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Chemical Structure| 39242-17-6
Chemical Structure| 39242-17-6
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Product Details of [ 39242-17-6 ]

CAS No. :39242-17-6 MDL No. :MFCD23103190
Formula : C11H9N5 Boiling Point : -
Linear Structure Formula :NC5H3(N2C3H3)2 InChI Key :RCULXUVDZWMPAS-UHFFFAOYSA-N
M.W : 211.22 Pubchem ID :12110747
Synonyms :

Safety of [ 39242-17-6 ]

Signal Word:Warning Class:
Precautionary Statements:P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313 UN#:
Hazard Statements:H315-H319 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 39242-17-6 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 39242-17-6 ]

[ 39242-17-6 ] Synthesis Path-Downstream   1~93

  • 2
  • [ 288-32-4 ]
  • [ 1513-65-1 ]
  • [ 39242-17-6 ]
  • 2-fluoro-6-(1H-imidazol-1-yl)pyridine [ No CAS ]
  • 3
  • [ 100-44-7 ]
  • [ 39242-17-6 ]
  • 1-Benzyl-3-(6-imidazol-1-yl-pyridin-2-yl)-3H-imidazol-1-ium; chloride [ No CAS ]
  • 4
  • [ 100-44-7 ]
  • [ 39242-17-6 ]
  • 2,6-Bis(3-benzylimidazol-3-ium-1-yl)pyridine dichloride [ No CAS ]
  • 5
  • [ 39242-17-6 ]
  • 1,1'-(pyridine-2,6-diyl)bis(3-benzyl-1H-imidazole-2-thione) [ No CAS ]
  • 6
  • [ 542-69-8 ]
  • [ 39242-17-6 ]
  • C19H27N5(2+)*2I(1-) [ No CAS ]
  • 7
  • [ 544-77-4 ]
  • [ 39242-17-6 ]
  • (C16H33C3N2H3)2C5NH3(2+)*2I(1-)=(C16H33C3N2H3)2C5NH3I2 [ No CAS ]
  • 8
  • [ 288-32-4 ]
  • [ 626-05-1 ]
  • [ 39242-17-6 ]
YieldReaction ConditionsOperation in experiment
78% With copper(I) oxide; (E)-pyridin-2-aldoxime; caesium carbonate; In acetonitrile; for 72h;Inert atmosphere; Reflux; After standard cycles of evacuation and back-fill with dry and pure nitrogen, an oven- dried Schlenk flask equipped with a magnetic stir bar was charged with Cu2O (0.1 mmol, 10 mol%), syn-2-pyridinealdoxime (0.4 mmol, 20 mol%), imidazole (2.5 mmol), Cs2CO3 (5 mmol), and 2,6-dibromopyridine (1.0 mmol), and anhydrous and degassed acetonitrile (80 mL). The flask was stirred in an oil bath, and refluxed for 3 days. The reaction mixture was allowed to cool to room temperature, diluted with dichloromethane and filtered through a plug of CELITE, the filter cake being further washed with dichloromethane (60 mL). The <n="32"/>filtrate was concentrated under vacuo to yield a residue, which was purified by column chromatography on silica gel to obtain the pure product DIz-Py in 78% yield. 1H NMR (CDCl3): £7.23 (s, 2H), 7.29 (d, 2H), 7.67 (s, 2H), 7.07 (t, 2H), 8.38 (s, 2H).
75% With potassium carbonate; In neat (no solvent); at 190℃; for 18h;Schlenk technique; Inert atmosphere; General procedure: A broad Schlenk tube equipped with a stirring bar was loaded with 2-halopyridine (if not other noted 2-bromopyridine) (1 eq.), imidazole (3 eq.) and K2CO3 (2 eq.). The reaction mixture was degassed to 10-3 mbar and put under argon atmosphere (Argon 6.0). Thereafter, the mixture stirred at 190C for 18h. After cooling to r.t. the mixture was diluted in water, extracted three times with chloroform and washed three times with saturated aqueous Na2CO3 solution. The combined organic phases were dried over MgSO4, filtrated and the solvent was removed under reduced pressure to leave a colorless oil or colorless solid.
50% With copper(l) iodide; potassium carbonate; N,N-dimethylethylenediamine; In dimethyl sulfoxide; at 20 - 110℃; for 36.5h;Glovebox; (A): The compound was synthesized with a modification from the reported procedure. ADDIN EN.CITE Wang201447[1]474717Wang, LeiLiu, NingDai, BinHu, HengcaiSelective C-N Bond-Forming Reaction of 2,6-Dibromopyridine with AminesEur. J. Org. Chem.Eur. J. Org. Chem.6493-650020142920141434-193X[1] A mixture of 2,6-dibromopyridine (400 mg, 1.69 mmole), imidazole (0.46 g, 6.75 mmole), K2CO3 (1.40 g, 10.12 mmole), CuI (0.13 g, 0.67 mmole), unsymmetrical N, N-dimethyl ethylenediamine (L3) (0.15 mL, 1.36 mmole) and dry-degassed dimethyl sulphoxide (5 mL) was added inside the glove box in a screw capped vial. The color of reaction mixture changed to blue, after the addition of L3. The reaction mixture was stirred for 30 minutes at ambient temperature and then, heated over a pre-heated oil bath at 110 C for 36 h. Subsequently, the reaction mixture was cooled down to ambient temperature and water (20 mL) was added to it. The product was extracted from this mixture by using dichloromethane. The organic phase was washed with water (3 times) and then, the organic phases were collected and washed with the brine solution (3 times) and then, dried over MgSO4. Dichloromethane was dried in vacuo to yield brown solids. Brown solids were purified by silica gel (100-200 Mesh) column chromatography using ethyl acetate: methanol: acetone (90: 6: 4, ν: ν: ν) as the eluent to afford white colored solid (0.18 g, 0.84 mmole). Yield: 50 %. 1H NMR (400 MHz, CDCl3, ppm) δ 8.41 (s, 2H, NCHN), 8.00 (dd, 3JC-H = 10.3, 3JC-H 5.7 Hz, 4H, imidazole- H), 7.70 (t, 4JC-H = 1.3 Hz, 1H, py-C4-H), 7.32 (d, 3JC-H = 8.0 Hz, 2H, py-C3,5-H).
With sodium carbonate; at 130℃; for 16h; 2 , 6-dibromopridine , imidazole and Na2CC>3 were mixed in a reactor using a 1:2.5:2.5 mole ratio. The reactor was then closed and heated to . 130C for 16 hrs . The reaction mixture was subsequently separated using column chromatography to obtain the product, sample le.

  • 9
  • copper(II) perchlorate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [Cu(2,6-bis(1'-imidazolo)pyridine)2](ClO4)2*2H2O [ No CAS ]
  • 10
  • [ 67-56-1 ]
  • [ 39242-17-6 ]
  • cobalt(II) perchlorate hexahydrate [ No CAS ]
  • [Co(2,6-bis(1'-imidazolo)pyridine)2](ClO4)2*MeOH [ No CAS ]
  • 11
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • zinc dibromide [ No CAS ]
  • dibromo(2,6-bis(imidazol-1-yl)pyridine)zinc(II)*0.25(hydrate) [ No CAS ]
  • dibromo(2,6-bis(imidazol-1-yl)pyridine)zinc(II)*0.25(hydrate) [ No CAS ]
  • 12
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • [ 7646-85-7 ]
  • dichloro(2,6-bis(imidazol-1-yl)pyridine)zinc(II) hemihydrate [ No CAS ]
  • dichloro(2,6-bis(imidazol-1-yl)pyridine)zinc(II) [ No CAS ]
  • 13
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • [ 7646-85-7 ]
  • dichloro(2,6-bis(imidazol-1-yl)pyridine)zinc(II) hemihydrate [ No CAS ]
  • dichloro(2,6-bis(imidazol-1-yl)pyridine)zinc(II) hemihydrate [ No CAS ]
  • 14
  • [ 67-56-1 ]
  • nickel(II) perchlorate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [Ni(2,6-bis(1'-imidazolo)pyridine)2](ClO4)2*MeOH [ No CAS ]
  • 15
  • manganese(II) perchlorate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [Mn(2,6-bis(1'-imidazolo)pyridine)2](ClO4)2*2H2O [ No CAS ]
  • 16
  • [ 39242-17-6 ]
  • [ 7646-85-7 ]
  • dichloro(2,6-bis(imidazol-1-yl)pyridine)zinc(II) [ No CAS ]
  • 17
  • [ 624-76-0 ]
  • [ 39242-17-6 ]
  • 1,1'-(2,6-pyridinediyl)bis[3-(2-hydroxyethyl)-1H-imidazol-3-ium] diiodide [ No CAS ]
  • 18
  • [ 109-09-1 ]
  • [ 39242-17-6 ]
  • C21H17N7(2+)*2F6P(1-) [ No CAS ]
  • 19
  • [ 39242-17-6 ]
  • [ 74-88-4 ]
  • [ 1187030-82-5 ]
YieldReaction ConditionsOperation in experiment
80% In toluene; at 20℃; for 96h; Methyl iodide (5 equiv) was syringed into a 50 mL round-bottomed flask charged with DIz-Py (10 mmol) and toluene (40 mL). The reaction was stirred under nitrogen in room temperature for 96h. Pale-yellow precipitate was formed. The precipitate was filtered, washed with toluene, washed with ether, and air-dried to obtain Iz-Py-IMIz in 80% yield. 1H NMR (DMSO): £3.98 (s, 3H), 7.20 (s, IH), 7.92 (d, IH), 7.96 (dd, IH), 8.00 (d, IH), 8.19 (s, IH), 8.37 (dd, IH), 8.64 (dd, IH), 8.84 (s, IH), 10.19 (s, IH).
  • 20
  • [ 623-24-5 ]
  • [ 39242-17-6 ]
  • cyclo[2](2,6-di(1H-imidazol-1-yl)pyridine)[2](1,4-dimethylenebenzene) tetrabromide [ No CAS ]
  • 21
  • [ 1120-71-4 ]
  • [ 39242-17-6 ]
  • [ 1266656-34-1 ]
YieldReaction ConditionsOperation in experiment
87% In acetonitrile; at 100℃; for 16h;Sealed tube; 2,6-Bis(l-imidazolyl)pyridine (0.538 g, 2.55 mmol) and 1,3-propane sultone (1.565 g, 12.8 mmol) were measured into a high pressure Pyrex tube. MeCN (10 mL) was added, and the vial was sealed and heated to 100 C for 16 hours. After cooling to room temperature, the white precipitate was collected via filtration and washed with copious amounts of DCM and MeOH. Ligand la was collected as a white powder (1.011 g, 0.540 mmol, 87%). NMR (400 MHz, D20) δ 9.93 (s, 2H), 8.53 - 8.44 (m, 1H), 8.43 - 8.37 (m, 2H), 8.05 (dt, J= 8.2, 1.1 Hz, 2H), 7.88 (dt, J = 2.2, 1.3 Hz, 2H), 4.61 (t, J = 7.1 Hz, 4H), 3.11 - 3.03 (m, 4H), 2.50 (p, J = 7.2 Hz, 4H).
87% In acetonitrile; at 100℃; for 16h; 2,6-Bis(1-imidazolyl)pyridine (0.538 g, 2.55 mmol)and 1,3-propane sultone (1.565 g, 12.8 mmol) were measured into ahigh pressure Pyrex tube. MeCN (10 mL) was added, and the vial wassealed and heated to 100 C for 16 hours, according to Scheme S2.After cooling to room temperature, the white precipitate was collectedvia filtration and washed with copious amounts of DCM and MeOH.Pro-ligand 1a was collected as a white powder (1.011 g, 0.540 mmol,87%).1H NMR (400 MHz, D2O) δ 9.93 (s, 2H), 8.53 - 8.44 (m, 1H),8.43 - 8.37 (m, 2H), 8.05 (dt, J = 8.2, 1.1 Hz, 2H), 7.88 (dt, J = 2.2, 1.3 Hz, 2H), 4.61 (t, J = 7.1Hz, 4H), 3.11 - 3.03 (m, 4H), 2.50 (p, J = 7.2 Hz, 4H).
  • 22
  • [ 6165-75-9 ]
  • [ 39242-17-6 ]
  • C17H15N5(2+)*F6P(1-) [ No CAS ]
  • 23
  • [ 875770-32-4 ]
  • [ 39242-17-6 ]
  • C33H47N5O8(2+)*2F6P(1-) [ No CAS ]
  • 24
  • [ 39242-17-6 ]
  • C38H34N10(4+)*C12H6O4(2-) [ No CAS ]
  • 25
  • [ 39242-17-6 ]
  • C38H34N10(4+)*4NO3(1-)*4H2O [ No CAS ]
  • 26
  • [ 623-24-5 ]
  • [ 39242-17-6 ]
  • cyclo[2](2,6-di(1H-imidazol-1-yl)pyridine)[2](1,4-dimethylenebenzene) hexafluorophosphate [ No CAS ]
  • 27
  • [ 39242-17-6 ]
  • [ 91-13-4 ]
  • cyclo[2](2,6-di(1H-imidazol-1-yl)pyridine)[2](1,2-dimethylenebenzene)hexafluorophosphate [ No CAS ]
  • 28
  • [ 39242-17-6 ]
  • [ 91-13-4 ]
  • C38H34N10(4+)*C12H6O4(2-) [ No CAS ]
  • 29
  • [ 39242-17-6 ]
  • [ 626-15-3 ]
  • cyclo[2](2,6-di(1H-imidazol-1-yl)pyridine)[2](1,3-dimethylenebenzene)hexafluorophosphate [ No CAS ]
  • 30
  • [ 7703-74-4 ]
  • [ 39242-17-6 ]
  • cyclo[2](2,6-di(1H-imidazol-1-yl)pyridine)[2](2,6-dimethylenepyridine)hexafluorophosphate [ No CAS ]
  • 31
  • [ 83-34-1 ]
  • [ 39242-17-6 ]
  • 3-[6-(1H-imidazol-1-yl)pyridin-2-yl]-1-(3-methyl-1H-indol-2-yl)-1H-imidazolium bromide [ No CAS ]
  • 32
  • [ 39242-17-6 ]
  • [ 106-95-6 ]
  • 1,1′-(pyridine-2,6-diyl)bis(3-allyl-1H-imidazol-3-ium) dibromide [ No CAS ]
  • 33
  • [ 4117-09-3 ]
  • [ 39242-17-6 ]
  • C25H35N5(2+)*2Br(1-) [ No CAS ]
  • 34
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [trans-Zn(2,6-bis(imidazol-1-yl)pyridine)2(NO3)2]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
36% In methanol; for 0.5h; To a solution of Zn(NO3)2·6H2O (0.074 g, 0.25 mmol) in methanol (40 mL), pyim2 (0.106, 0.5 mmol) was added as solid and the solution was stirred for 30 min. The solution was allowed to evaporate at room temperature very slowly to afford colourless crystals after few weeks. Yield: 0.055 g, 36 % based on Zn(NO3)2·6H2O. Anal. calcd. for C22H18N12O6Zn (611.85): C, 43.19; H, 2.96; N, 27.47. Found: C, 42.50; H, 2.73; N, 28.00. IR (KBr, cm-1): 3182 (s), 3168 (s), 3136 (vs), 3119 (vs), 1606 (vs), 1585 (vs), 1502 (vs), 1462 (vs), 1420 (vs), 1309 (vs), 1254 (vs), 1238 (s), 1178 (s), 1139 (vs), 1120 (vs), 1073 (s), 1039 (s), 1007 (s), 837 (s), 805 (s), 777 (s), 763 (s), 675 (s), 658 (m), 532 (w).
  • 35
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [trans-Zn(2,6-bis(imidazol-1-yl)pyridine)2(H2O)2]*(NO3)2}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
34% In methanol; water; N,N-dimethyl-formamide; at 20℃; for 48h; To a solution of Zn(NO3)2·6H2O (0.074 g, 0.25 mmol) in DMF (4 mL), a solution of pyim2 (0.106 g, 0.5 mmol) in methanol (8 mL) was layered. Further, distilled H2O (25 mL) was layered over the top of this solution. The solution was allowed to stand at room temperature to afford colourless crystals in two days. Yield 0.11 g, 34% based on Zn(NO3)2·6H2O.Anal. calcd. for C22H22N12O8Zn (647.89): C, 40.78; H,3.42; N, 25.94. Found: C, 40.92; H, 3.33; N, 25.58. IR(KBr, cm-1): 3387 (br), 3260 (br), 3128 (s), 1729 (w),1672 (w), 1606 (vs), 1589 (m), 1493 (vs), 1462 (vs),1388 (vs), 1348 (vs), 1289 (vs), 1253 (s), 1242 (vs),1180 (m), 1137 (w), 1110 (m), 1081 (m), 1070 (s), 1006(m), 993 (w), 963 (w), 930 (m), 868 (m), 826 (w), 802(s), 759 (s), 677 (s), 659 (w), 620 (w), 537(br).1H-NMR(DMSO-d6, 500 MHz, δ): 7.12 (s, 2H, H4-Im), 7.72 (d,J = 10 Hz, 2H, H3-Py), 8.10 (s, 2H, H5-Im), 8.14 (t, J= 25 Hz, 1H, H4-Py), 8.72 (s, 2H, H2-Im).
  • 36
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [trans-Cd(2,6-bis(imidazol-1-yl)pyridine)2(NO3)2]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
62% In methanol; N,N-dimethyl-formamide; at 20℃; Pyim2 (0.053, 0.25 mmol) in methanol (2 mL) was layered over a solution of Cd(NO3)2·4H2O (0.039 g, 0.125 mmol) in DMF (1 mL). The solution was allowed to stand at room temperature to afford colourless crystals. The same product was obtained, if this reaction was carried out only in methanol. Yield: 62% based on Cd(NO3)2·4H2O. Anal. Calcd. for C22H18N12O6Cd (658.88): C, 40.10; H, 2.75; N, 25.51. Found: C, 39.49; H, 2.27; N, 25.03. IR (KBr, cm-1): 3159 (w), 2923 (w), 2853 (w), 1606 (s), 1585 (s), 1498 (vs), 1463 (vs), 1422 (s), 1310 (vs), 1250 (vs), 1236 (m), 1178 (m), 1139 (m), 1115 (m), 1070 (s), 1039 (s), 1007(s), 992 (m), 964 (m), 929 (m), 882 (m), 833 (m), 807 (m), 777 (m), 764 (m), 753 (m), 674 (m), 655 (m), 621 (m), 533 (w), 469 (w).
  • 37
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [trans-Cd(2,6-bis(imidazol-1-yl)pyridine)2(H2O)2]·(NO3)2}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
71% In methanol; water; N,N-dimethyl-formamide; at 20℃; for 24h; General procedure: To a solution of Zn(NO3)2·6H2O (0.074 g, 0.25 mmol) in DMF (4 mL), a solution of pyim2 (0.106 g, 0.5 mmol) in methanol (8 mL) was layered. Further, distilled H2O (25 mL) was layered over the top of this solution. The solution was allowed to stand at room temperature to afford colourless crystals in two days.
  • 38
  • cadmium(II) nitrate hexahydrate [ No CAS ]
  • [ 2449-35-6 ]
  • [ 39242-17-6 ]
  • [Cd(4,4'-sulfonyldibenzoato)(2,6-bis(1-imdazoly)pyridine)]*1.5(H2O) [ No CAS ]
YieldReaction ConditionsOperation in experiment
32% With sodium hydrogencarbonate; In water; at 160℃; for 72h;Autoclave; A mixture of Cd(NO3)26H2O (0.030 g, 0.1 mmol), 4,40-H2sdb(0.025 g, 0.1 mmol), NaHCO3 (0.016 g, 0.2 mmol) and H2O (10 mL)was placed in a 23 mL Teflon-lined stainless steel reactor underautogenous pressure at 160 C for 72 h and then cooled to roomtemperature slowly. Colorless block crystals were obtained in 32%yield based on Cd(NO3)24H2O. Anal. calcd. for C50H40Cd2N10O15S2(1309.86): C, 45.81; H, 3.05; N, 10.69%. Found: C, 45.87; H, 3.12; N,10.62%. IR (cm1): 3422(w), 1712(m), 1675(s), 1587(m), 1509(m),1389(m), 1378(m), 1109(w), 1025(w), 958(m), 893(m), 826(m),778(w), 690(w), 674(w), 589(w), 562(w).
  • 39
  • cadmium(II) nitrate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [ 2904-41-8 ]
  • Cd<SUB>2</SUB>(tri(2-carboxyethyl)isocyanurate(-2H))<SUB>2</SUB>(2,6-bis(1-imdazoly)pyridine)<SUB>2</SUB> [ No CAS ]
YieldReaction ConditionsOperation in experiment
38% With sodium hydrogencarbonate; In water; at 160℃;Autoclave; The synthesis of compound 2 was similar to that of 1, but withH3tci (93 mg, 0.1 mmol) in place of 4,40-H2sdb. Colorless crystals of2 were obtained in 38% yield based on Cd(NO3)24H2O. Elementalanalyses calcd. for C46H44Cd2N16O18 (1333.79): C, 41.39; H, 3.30; N,16.79%. Found: C, 41.36; H, 3.27; N, 16.71%. IR data (KBr pellet):3450(s), 3179(m), 1652(m), 1626(m), 1550(s), 1478(s), 1431(m),1182(s), 1135(m), 1034(m), 826(w), 807(m), 787(w), 610(m),550(m), 519(m), 486(w).
  • 40
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 554-95-0 ]
  • [ 39242-17-6 ]
  • [Zn2(1,3,5-benzenetricarboxylato)(2,6-bis(1-imdazoly)pyridine)(OH)]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
32% A mixture of Zn(NO3)26H2O (0.06 g, 0.20 mmol), H3btc (0.021 g,0.10 mmol), biimpy (0.021 g, 0.1 mmol), NaHCO3 (0.025 g,0.3 mmol) and H2O (8 mL) was placed in a 23 mL Teflon liner. Theresulting mixture was stirred for 30 min at room temperature, andthen the mixture was sealed in a Parr autoclave and kept at 120 Cfor four days. After being slowly cooled to the room temperature,colorless prism crystals of 1 were isolated. Yield: 32% based onZn(II). Anal. calc. for C20H13N5O7Zn2 (566.13): C, 42.39; N, 12.36; H,2.30%. Found: C, 42.44; N, 12.42; H, 2.23%. IR (KBr pellet, cm1) for1: 3421(w), 1647(w), 1562(s), 1481(w), 1428(m), 1358(s), 1312(w),1256(w), 1138(w), 1124(m), 1051(s), 997(w), 917(w), 783(s), 726(s).
  • 41
  • [ 17084-13-8 ]
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [Zn(2,6-bis(imidazol-1-yl)pyridine)2]·(PF6)2}n [ No CAS ]
  • 42
  • [ 17084-13-8 ]
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • [trans-Cd(2,6-bis(imidazol-1-yl)pyridine)2(DMF)2]·(PF6)2·(DMF)2}n [ No CAS ]
  • 43
  • [ 17084-13-8 ]
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • [trans-Cd(2,6-bis(imidazol-1-yl)pyridine)2(H2O)2]·(PF6)·(NO3)2·(H2O)2}n [ No CAS ]
  • 44
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • [trans-Cd(2,6-bis(imidazol-1-yl)pyridine)2(H2O)2]·(NO3)2}n [ No CAS ]
  • 45
  • zinc(II) acetate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • [ 2904-41-8 ]
  • [Zn3(tri(2-carboxyethyl)isocyanurate)2(2,6-bis(1-imidazolyl)pyridine)]n*2n(N,N-dimethylformamide) [ No CAS ]
YieldReaction ConditionsOperation in experiment
46% In water; at 110℃; for 72h;Autoclave; [Zn3(tci)2(biimpy)]n*2n(DMF) (1) was prepared as follows. A mixture of Zn(NO3)2*6H2O (0.2 mmol, 0.06 g), H3tci (0.034 g,0.1 mmol), biimpy (0.021 g, 0.1 mmol), DMF (2 mL), and H2O (2 mL) were sealed in a 20-mL small vial and heated at 110C for 3 days. After cooling to room temperature, colourless crystals of 1 were obtained (46% yield based on H3tci). νmax (KBr)/cm-1 3447 (m), 2426 (w), 1685 (s), 1632 (s), 1463 (w), 1381 (vs), 1221 (w), 1064 (w), 834 (m), 764 (m). Found: C 39.70, H 3.86, N 14.67. C41H47N13O20Zn3 requires C 39.74, H 3.80, N 14.70 %.
  • 46
  • [ 39242-17-6 ]
  • C30H36AuN10(3+)*3BF4(1-) [ No CAS ]
  • 47
  • [ 39242-17-6 ]
  • C30H34AgAuN10(2+)*2BF4(1-) [ No CAS ]
  • 48
  • [ 39242-17-6 ]
  • C30H34AuHgN10(3+)*3BF4(1-) [ No CAS ]
  • 49
  • [ 39242-17-6 ]
  • C30H34AuCuN10(2+)*2BF4(1-) [ No CAS ]
  • 50
  • [ 39242-17-6 ]
  • C30H34Cu2N10(2+)*2BF4(1-) [ No CAS ]
  • 51
  • [ 39242-17-6 ]
  • C30H34Ag2N10(2+)*2BF4(1-) [ No CAS ]
  • 52
  • [ 39242-17-6 ]
  • C30H34Au2N10(2+)*2BF4(1-) [ No CAS ]
  • 53
  • [ 39242-17-6 ]
  • C30H34Hg2N10(4+)*4BF4(1-) [ No CAS ]
  • 54
  • [ 39242-17-6 ]
  • C26H26AuN10(1+)*BF4(1-) [ No CAS ]
  • 55
  • [ 368-39-8 ]
  • [ 39242-17-6 ]
  • C13H15N5(2+)*2BF4(1-) [ No CAS ]
  • 56
  • [ 74-96-4 ]
  • [ 39242-17-6 ]
  • C13H14N5(1+)*Br(1-) [ No CAS ]
  • 57
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 2215-89-6 ]
  • [ 39242-17-6 ]
  • [Zn(2,6-dis(imidazol-1-yl)pyridine)(OBA)]·(H2O)}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% In methanol; N,N-dimethyl-formamide; at 20℃; for 168h; To a solution of pyim2 (0.042 g, 0.2 mmol) in methanol (5 mL), a solution of H2OBA (0.025 g, 0.1 mmol) in DMF (3 mL) was layered, followed by a solution of Zn(NO3)2·6H2O (0.029 g, 0.1 mmol) in methanol (5 mL). The solution was allowed to stand at RT to afford colorless crystals in seven days. Yield: 0.040 g, 72% based on Zn(NO3)2·6H2O. Anal. Calc. for C25H19N5O6Zn (550.85): C, 54.51; H, 3.48; N, 12.71. Found: C, 54.59; H, 3.55; N, 12.74%. IR (KBr, cm-1): 3458 (w), 3128 (w), 3066 (w), 2925 (w), 2854 (br), 1717 (w), 1674 (m), 1603 (vs), 1560 (s), 1499 (vs), 1465 (s), 1372 (vs), 1313 (m), 1301 (m), 1282 (s), 1238 (vs), 1188 (w), 1159 (s), 1114 (w), 1096 (w), 1080 (m), 1067 (m), 1010 (m), 996 (br), 965 (br), 946 (w), 880 (m), 856 (w), 835 (w), 785 (s), 766 (m), 734 (w), 712 (br), 697 (br), 649 (s), 632 (br), 621 (w), 553 (br), 521 (br), 434 (br).
  • 58
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 2215-89-6 ]
  • [ 39242-17-6 ]
  • [Cd(2,6-dis(imidazol-1-yl)pyridine)(OBA)]·(H2O)}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
90% In N,N-dimethyl-formamide; at 20℃; for 24h; To a solution of Cd(NO3)2·4H2O (0.030 g, 0.1 mmol) in DMF (1 mL), a solution of pyim2 (0.042 g, 0.2 mmol) in methanol (2 mL) was layered, followed by layering a H2OBA (0.025 g, 0.1 mmol) solution in DMF (1 mL). The solution was allowed to stand at RT to afford colorless crystals in one day. Yield: 0.057 g, 90% based on Cd(NO3)2·4H2O. Anal. Calc. for C25H19CdN5O6 (597.86): C, 50.22; H, 3.20; N, 11.71. Found: C, 50.31; H, 3.28; N, 11.75%. IR (KBr, cm-1): 3424 (br), 3159 (m), 3131 (m), 3120 (m), 2348 (br), 1678 (m), 1604 (vs), 1559 (s), 1546 (s), 1494 (vs), 1462 (vs), 1391 (vs), 1313 (s), 1298 (s), 1282 (s), 1264 (m), 1236 (vs), 1177 (m), 1161 (m), 1138 (w), 1084 (w), 1069 (m), 1040 (w), 1008 (s), 992 (w), 963 (w), 929 (w), 878 (m), 855 (m), 827 (m), 805 (m), 792 (m), 781 (s), 764 (s), 725 (s), 706 (w), 694 (w), 656 (m), 643 (m), 619 (w), 524 (w), 432 (br), 407 (br).
  • 59
  • [ 67-56-1 ]
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • [ 88-99-3 ]
  • [Zn(2,6-dis(imidazol-1-yl)pyridine)(o-BDC)]·(DMF)(MeOH)}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
77% at 20℃; for 240h; To a solution of pyim2 (0.042 g, 0.2 mmol) in methanol (2 mL), a solution of Zn(NO3)2·6H2O (0.029 g, 0.1 mmol) in DMF (1 mL) was layered, followed by a solution of H2o-BDC (0.016 g, 0.1 mmol) in DMF (1 mL). The solution was allowed to stand at RT to afford colorless crystals in ten days. Yield: 0.041 g, 77% based on Zn(NO3)2·6H2O. Anal. Calc. for C23H24N6O6Zn (545.88): C, 50.61; H, 4.43; N, 15.40. Found: C, 50.89; H, 4.98; N, 15.525%. IR (KBr, cm-1): 3443 (w), 3118 (m), 3147 (w), 2852 (w), 1668 (s), 1607 (vs), 1587 (vs), 1537 (w), 1498 (vs), 1465 (vs), 1355 (vs), 1325 (m), 1310 (s), 1296 (s), 1282 (s), 1261 (m), 1242 (m), 1234 (m), 1176 (w), 1144 (w), 1105 (m), 1078 (s), 1067 (s), 1012 (m), 966 (w), 946 (m), 886 (br), 858 (br), 798 (m), 778 (m), 764 (m), 703 (m), 647 (m), 621 (w), 481 (br).
  • 60
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 121-91-5 ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • [Zn2(2,6-dis(imidazol-1-yl)pyridine)2(m-BDC)2]·(DMF)4}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
72% In methanol; at 20℃; for 216h; To a solution of Zn(NO3)2·6H2O (0.029 g, 0.1 mmol) in DMF (3 mL), a solution of pyim2 (0.042 g, 0.2 mmol) in methanol (4 mL) was layered followed by a solution of H2m-BDC (0.016 g, 0.1 mmol) in DMF (4 mL). The solution was allowed to stand at RT to afford colorless crystals in nine days. Yield: 0.041 g, 72% based on Zn(NO3)2·6H2O. Anal. Calc. for C50H54N14O12Zn2 (1173.81): C, 51.16; H, 4.64; N, 16.70. Found: C, 51.19; H, 4.68; N, 16.72%. IR (KBr, cm-1): 3559 (w), 3506 (w), 3160 (w), 3105 (w), 1622 (vs), 1623 (s), 1606 (s), 1585 (vs), 1537 (w), 1498 (vs), 1484 (vs), 1462 (vs), 1426 (m), 1385 (vs), 1357 (vs), 1290 (s), 1266 (s), 1232 (s), 1186 (m), 1151 (w), 1114 (m), 1077 (s), 1065 (s), 1003 (m), 966 (w), 942 (w), 911 (br), 843 (w), 829 (w), 804 (m), 764 (m), 742 (s), 723 (s), 652 (s), 619 (w), 566 (br), 475 (br).
  • 61
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 100-21-0 ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • [Zn(2,6-dis(imidazol-1-yl)pyridine)(p-BDC)]·(DMF)}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
74% In methanol; at 20℃; for 72h; To a solution of Zn(NO3)2·6H2O (0.029 g, 0.1 mmol) in DMF (1 mL), a solution of pyim2 (0.042 g, 0.2 mmol) in methanol (2 mL) was layered, followed by a solution of H2p-BDC (0.016 g, 0.1 mmol) in DMF (1 mL). The solution was allowed to stand at RT to afford colorless crystals in three days. Yield: 0.037 g, 74% based on Zn(NO3)2·6H2O. Anal. Calc. for C22H20N6O5Zn (513.81): C, 51.42; H, 3.92; N, 16.36. Found: C, 51.49; H, 3.94; N, 16.38%. IR (KBr, cm-1): 3433 (br), 3138 (w), 3101 (w), 1678 (w), 1602 (vs), 1502 (vs), 1462 (s), 1385 (s), 1358 (vs), 1339 (vs), 1320 (s), 1282 (s), 1248 (s), 1235 (m), 1175 (w), 1138 (w), 1108 (m), 1090 (m), 1068 (s), 1011 (m), 994 (w), 966 (w), 945 (m), 886 (w), 846 (m), 827 (s), 816 (m), 809 (s), 782 (w), 767 (m), 747 (s), 737 (s), 673 (br), 661 (m), 651 (m), 617 (br), 577 (m), 514 (w), 507 (w).
  • 62
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 100-21-0 ]
  • [ 39242-17-6 ]
  • [Cd(2,6-dis(imidazol-1-yl)pyridine)(p-BDC)(H2O)]·(H2O)2}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% In methanol; water; N,N-dimethyl-formamide; at 20℃; for 168h; To a solution of Cd(NO3)2·4H2O (0.030 g, 0.1 mmol) in DMF (1 mL), a solution of pyim2 (0.042 g, 0.2 mmol) in methanol (2 mL) was layered, followed by a solution of H2p-BDC (0.016 g, 0.1 mmol) in DMF (1 mL). Distilled H2O (10 mL) was finally layered over the top of the solution. The solution was allowed to stand at RT to afford colorless crystals in seven days. Yield: 0.053 g, 70% based on Cd(NO3)2·4H2O. Anal. Calc. for C30H31CdN10O9 (788.05): C, 45.72; H, 3.97; N, 17.77. Found: C, 45.49; H, 3.98; N, 17.52%. IR (KBr, cm-1): 3339 (s), 3160 (s), 3140 (s), 3121 (s), 1606 (vs), 1588 (s), 1568 (vs), 1493 (vs), 1479 (vs), 1462 (vs), 1389 (vs), 1323 (s), 1291 (s), 1275 (m), 1240 (m), 1231 (s), 1189 (m), 1144 (w), 1107 (m), 1077 (s), 1059 (s), 1004 (m), 964 (w), 931 (m), 891 (w), 841 (s), 798 (s), 755 (s), 736 (s), 651 (s), 616 (m), 523 (w).
  • 63
  • manganese(II) chloride monohydrate [ No CAS ]
  • [ 10312-55-7 ]
  • [ 39242-17-6 ]
  • [Mn(2,6-bis(1-imidazoly)pyridine)(2-aminoterephthalate)]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
45% In water; N,N-dimethyl-formamide; at 20 - 110℃; for 72.5h;High pressure; Synthesis of [Mn(impy)(NH2-pbc)]n (1). A mixture ofMnCl2.4H2O (0.016 g, 0.10 mmol), NH2-H2pbc (0.018 g,0.10 mmol), impy (0.021 g, 0.1mmol), H2O (2 mL), andDMF (2 mL) was placed in a 20 mL small vial. The resultingmixture was stirred for 30 min at room temperature, andthen the mixture was kept at 110C for three days. Afterbeing slowly cooled to the room temperature at a rate of5C/h, colorless prism crystals of1were isolated (Yielding45% based on Mn(II). Anal. Calcd. for C38H26Mn2N13O8 (902.60): C, 50.52; N, 20.16; H, 2.88%. Found: C, 50.58; N,20.18; H, 2.84%. IR (cm1): 3412(s), 1649(m), 1573 (s), 1512(w), 1451(m), 1398(s), 1131(s), 1017(w), 880(w), 750 (w),626 (m), 504(w).
  • 64
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 1934-75-4 ]
  • [ 39242-17-6 ]
  • {Cd(2,6-bis(imidazol-1-yl)pyridine)[N(CN)2]2}n [ No CAS ]
YieldReaction ConditionsOperation in experiment
38.3% Synthesis of {Cd(2,6-bip)[N(CN)2]2}n 2 2,6-bip (0.5 mmol, 0.1056 g) and NaN(CN)2 (1 mmol, 0.0890 g) were added into 3 mL methanol and the solution was stirred for 10 min. After filtration, the solution was carefully layered on the surface of 5 mL DMSO solution containing Cd(NO3)2·4H2O (0.4 mmol, 0.1234 g). Several days later, 2 was obtained as colorless square crystals. Yield: 0.0698 g (38.30% based on Cd). Anal. Calc. for C15H9CdN11: C, 39.53; H, 1.99; N, 33.81%. Found: C, 39.20; H, 2.04; N, 33.54%. IR (KBr pellet, cm-1): 2159(s), 1605(s), 1493(s), 1464(s).
  • 65
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 1147550-11-5 ]
  • [ 39242-17-6 ]
  • [Cd(2,6-bis(imidazol-1-yl)pyridine)2(NCS)2]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
37.78% Synthesis of [Cd(2,6-bip)2(NCS)2]n 1 2,6-bip (0.5 mmol, 0.1056 g) and NH4SCN (0.5 mmol, 0.0381 g) were added into 3 mL methanol and the solution was stirred for 10 min. After filtration, the solution was carefully layered on the surface of 5 mL DMF solution containing Cd(NO3)2·4H2O (0.4 mmol, 0.1234 g). Several days later, 1 was obtained as colorless blocky crystals. Yield: 0.0984 g (37.78% based on Cd). Anal. Calc. for C24H18CdN12S2: C, 44.28; H, 2.79; N, 25.82%. Found: C, 44.31; H, 2.80; N, 25.79%. IR (KBr pellet, cm-1): 2158(s), 1606(m), 1493(s), 1284(s), 1061(m), 803(w).
  • 66
  • [ 39242-17-6 ]
  • C17H20N6Pd(2+)*2F6P(1-) [ No CAS ]
  • 67
  • [ 39242-17-6 ]
  • C15H17BrN5Pd(1+)*Br(1-) [ No CAS ]
  • 68
  • [ 74-96-4 ]
  • [ 39242-17-6 ]
  • 2,6-bis[3-(ethyl)imidazolium]pyridine dibromide [ No CAS ]
YieldReaction ConditionsOperation in experiment
94% at 150℃; for 96h;Sealed tube; The preparation of this compound was based on previously published methods [19,23]. 2,6-Bis(1-imidazolyl)pyridine (0.201g, 0.095mmol), bromoethane (0.70ml, 0.94mmol), and 3.0mL of xylenes were added to a thick-walled glass tube. The tube was sealed with a screw top cap equipped with a rubber o-ring and the vessel was heated at 150C for 4days. After cooling the reaction mixture to room temperature, the resulting material was triturated several times with ether and the solid was collected to yield 0.386g of an off white solid. Yield=94%. 1H NMR (400MHz, DMSO-d6, 25C) δ/ppm: 10.74 (s, 2H), 8.88 (s, 2H), 8.61 (t, J=8.1Hz, 1H), 8.29 (d, J=8.1Hz, 2H), 8.21 (s, 2H), 4.40 (q, J=7.3Hz, 4H), 1.55 (t, J=7.3Hz, 6H). 13C NMR (101MHz, DMSO, 25C) δ/ppm: 145.31, 144.84, 135.66, 123.52, 119.39, 114.12, 45.15, 15.03. HR-LIFDI-MS [M-Br]+ m/z: calculated for C15H19N5Br 348.0824; found, 348.0830.
  • 69
  • [ 39242-17-6 ]
  • [ 74-88-4 ]
  • 2,6-bis(methylimidazolium)pyridine diiodide [ No CAS ]
  • 70
  • [ 39242-17-6 ]
  • C50H42Au2N10(2+)*2F6P(1-) [ No CAS ]
  • 71
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 39242-17-6 ]
  • [ 2904-41-8 ]
  • [Cd(Htci)(2,6-bis(1-imdazoly)pyridine)]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
38% With sodium hydroxide; In water; at 120℃; for 72h;pH 6;Autoclave; High pressure; In a 23mL Teflon lined stainless steel container, Cd(NO3)2·4H2O (0.2mmol, 0.06g), H3tci (0.034g, 0.1mmol) and biimpy (0.021g, 0.1mmol) were dissolved in 10mLH2O, and then adjust the pH to 6.0 using 0.2mL 1mol/L NaOH solution. Then, the mixture was heated to 120C and held at this temperature for 72h. After cooling slowly to the room temperature, yellow prism crystals were obtained in 38% yield. Anal. Calc. for 1 C23H21CdN8O9: C, 41.45; H, 3.15; N, 16.82. Found: C, 41.53; H, 3.12; N, 16.87. IR/cm-1(KBr): 3412 (m), 1615 (s), 1592 (s), 1548 (s), 1516 (m), 1428 (m), 1367 (s), 1261 (m), 1227 (s), 1072 (w), 967 (m), 845 (m), 772 (w), 746 (w), 653 (w).
  • 72
  • cadmium(II) nitrate tetrhydrate [ No CAS ]
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • [ 2904-41-8 ]
  • [Cd3(tci)2(2,6-bis(1-imdazoly)pyridine)2(H2O)2]n [ No CAS ]
YieldReaction ConditionsOperation in experiment
42% With sodium hydroxide; at 120℃; for 72h;pH 8;Autoclave; High pressure; General procedure: In a 23mL Teflon lined stainless steel container, Cd(NO3)2·4H2O (0.2mmol, 0.06g), H3tci (0.034g, 0.1mmol) and biimpy (0.021g, 0.1mmol) were dissolved in 10mLH2O, and then adjust the pH to 6.0 using 0.2mL 1mol/L NaOH solution. Then, the mixture was heated to 120C and held at this temperature for 72h. After cooling slowly to the room temperature, yellow prism crystals were obtained in 38% yield.
  • 73
  • [ 39242-17-6 ]
  • C39H34N10O2(4+)*4F6P(1-) [ No CAS ]
  • 74
  • [ 39242-17-6 ]
  • C39H34N10O2(4+)*4Cl(1-) [ No CAS ]
  • 75
  • [ 623-24-5 ]
  • [ 39242-17-6 ]
  • C27H25Br2N5(2+)*2F6P(1-) [ No CAS ]
  • 76
  • [ 10196-18-6 ]
  • [ 42178-86-9 ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • [Zn(4,4'-(4-phenylpyridine-2,6-diyl)dibenzoate)(2,6-di(1H-imidazol-1-yl)pyridine)]·DMF [ No CAS ]
  • 77
  • [ 181188-86-3 ]
  • [ 10196-18-6 ]
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • [Zn(4,4'-(phenylazanediyl)dibenzoate)(2,6-di(1H-imidazol-1-yl)pyridine)]·2H2O·DMF [ No CAS ]
  • 78
  • [ 42178-86-9 ]
  • [ 39242-17-6 ]
  • cobalt(II) nitrate [ No CAS ]
  • [ 33513-42-7 ]
  • [Co(4,4'-(4-phenylpyridine-2,6-diyl)dibenzoate)(2,6-di(1H-imidazol-1-yl)pyridine)]·DMF [ No CAS ]
  • 79
  • [ 181188-86-3 ]
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • cobalt(II) nitrate [ No CAS ]
  • [ 33513-42-7 ]
  • [Co(4,4'-(phenylazanediyl)dibenzoate)(2,6-di(1H-imidazol-1-yl)pyridine)]·H2O·DMF [ No CAS ]
  • 80
  • [ 42178-86-9 ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • cadmium(II) nitrate [ No CAS ]
  • [Cd(4,4'-(4-phenylpyridine-2,6-diyl)dibenzoate)(2,6-di(1H-imidazol-1-yl)pyridine)]·DMF [ No CAS ]
  • 81
  • [ 181188-86-3 ]
  • [ 39242-17-6 ]
  • cadmium(II) nitrate [ No CAS ]
  • [Cd(4,4'-(phenylazanediyl)dibenzoate)(2,6-di(1H-imidazol-1-yl)pyridine)] [ No CAS ]
  • 82
  • [ 39242-17-6 ]
  • C29H45B2N5O4(2+)*2C24H20B(1-) [ No CAS ]
  • 83
  • [ 39242-17-6 ]
  • C35H52B2FeN8O4(2+)*2C24H20B(1-) [ No CAS ]
  • 84
  • [ 39242-17-6 ]
  • C31H43B2FeN5O6 [ No CAS ]
  • 85
  • [ 39242-17-6 ]
  • [ 124215-44-7 ]
  • C29H45B2N5O4(2+)*2Br(1-) [ No CAS ]
  • 86
  • [ 39242-17-6 ]
  • [ 97654-99-4 ]
  • C50H42N14(4+)*4Br(1-) [ No CAS ]
  • 87
  • [ 39242-17-6 ]
  • [ 501-65-5 ]
  • 4,5,7,8-detraphenylimidazo[1',2':1,6]pyrido[3,2-g]imidazo[1,2-a][1,8]naphthyridine [ No CAS ]
  • 88
  • [ 1942-45-6 ]
  • [ 39242-17-6 ]
  • 4,5,7,8-tetrapropylimidazo[1',2':1,6]pyrido[3,2-g]imidazo[1,2-a][1,8]naphthyridine [ No CAS ]
  • 89
  • [ 10034-85-2 ]
  • [ 39242-17-6 ]
  • [ 33513-42-7 ]
  • [ 7681-11-0 ]
  • silver(I) iodide [ No CAS ]
  • C11H9N5*2H(1+)*2Ag(1+)*3I(1-)*CHO(1-) [ No CAS ]
  • 90
  • [ 39242-17-6 ]
  • C35H27CuIN5P2*CH2Cl2 [ No CAS ]
  • 91
  • [ 39242-17-6 ]
  • [{2,6-{PPh2C3H2N2}2C5H3N}{AuCl}2] [ No CAS ]
  • 92
  • [ 1079-66-9 ]
  • [ 39242-17-6 ]
  • [2,6-(PPh2-C3H2N2)2C5H3N] [ No CAS ]
  • 93
  • zinc(II) nitrate hexahydrate [ No CAS ]
  • [ 7732-18-5 ]
  • [ 39242-17-6 ]
  • [ 65697-90-7 ]
  • [Zn5(3,5-bis(4′-carboxylatophenyl)-1,2,4-triazole)2(2,6-bis(imidazole-1-yl)pyridine)22-OH)4]·5H2O} [ No CAS ]
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