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Chemical Structure| 1232101-98-2 Chemical Structure| 1232101-98-2

Structure of 1232101-98-2

Chemical Structure| 1232101-98-2

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Product Details of [ 1232101-98-2 ]

CAS No. :1232101-98-2
Formula : C26H20BNO2
M.W : 389.25
SMILES Code : OB(C1=CC=C(NC2=CC=C3C=CC=CC3=C2C4=C5C=CC=CC5=CC=C4)C=C1)O

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Application In Synthesis of [ 1232101-98-2 ]

* 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 [ 1232101-98-2 ]

[ 1232101-98-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 1232101-98-2 ]
  • [ 4181-20-8 ]
  • tris-{4-[(naphthalen-1-yl(naphthalen-2-yl)amino)]biphenyl}amine [ No CAS ]
YieldReaction ConditionsOperation in experiment
32% With tetrakis(triphenylphosphine) palladium(0); tri-tert-butyl phosphine; potassium carbonate; In water; toluene; at 100℃; for 2h;Inert atmosphere; General procedure: A mixture of 9-(3-(9H-carbazol-9-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-9H-carbazole 1 (3.9 g,7.30 mmol), <strong>[4181-20-8]tris(4-iodophenyl)amine</strong> 3b (1 g, 1.61 mmol),Pd(Ph3P)4 (0.37 g, 0.32mmol), t-Bu3P 50percent in toluene(0.3 mL, 0.64mmol), and K2CO3 (4.4 g, 31.8 mmol) in 100 mL of toluene and 50 mL of distilled water was stirred at 100°C for 2 days under argon. After completion of the reaction,the mixture was extracted with dichloromethane. The organic layers were then separated, dried over magnesium sulfate, filtered,and concentrated. The residues were purified by column chromatography using silica gel as the stationary phase and an n-hexane: dichloromethanemixture as the eluent to give the requisiteproduct 4b. Yield: 40percent;
32% With tetrakis(triphenylphosphine) palladium(0); tri-tert-butyl phosphine; potassium carbonate; In toluene; at 100℃; for 48h;Inert atmosphere; 4-(N-(naphthalen-2-yl)-N-(naphthalen-4-yl)amino)phenylboronic acid (2.84 g, 7.30 mmol) in toluene (100 ml) and distilled water (50 ml) Pd (Pd3P)4(0.37 g, 0.32 mmol), t-Bu3P intoluene(0.3 ml, 0.64 mmol) and K2CO3(4.4 g, 31.8 mmol) was stirred at 100 ° C. for 2 days under argon atmosphere.After completion of the reaction, the mixture was extracted with dichloromethane.Then, the organic layer was separated, MgSO4was then dried filtered and concentrated.The resulting residue was purified by silica gel column chromatography using n-hexane: dichloromethane as an eluent to obtain a product of formula (2b) as a yellow solid (yield: 32percent).
  • 2
  • [ 1232101-98-2 ]
  • [ 171408-84-7 ]
  • N,N'-(9,9'-spirobi[fluorene]-2,7-diylbis(4,1-phenylene))bis(N-(naphthalene-2-yl)naphthalene-1-amine) [ No CAS ]
YieldReaction ConditionsOperation in experiment
64.4% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In toluene; at 110℃; for 24h; A mixture of 2,7-dibromo-9,9'-spirobifluorene (1, 1 g, 1 equiv.), 4-(N-(naphthalen-2-yl)-N-(naphthalen-4-yl)amino)phenylboronic acid (B, 2.5 g, 3 equiv.), Pd(Ph3P)4 (0.09 g, 0.2 equiv.),K2CO3 (2 M, 50 mL) and toluene (100 mL) were mixed and then stirred at 110° C for 24 h.After completion of the reaction, the reaction mixture was extracted with dichloromethane and water.The organic layer was dried over anhydrous magnesium sulphate then filtered and concentratedby rotary evaporation. The crude residue was purified by silica gel column chromatography usinga n-hexanedichloromethane solvent system to provide pure HTM 1B. Yield: 64.4percent; yellow solid;1H-NMR (CDCl3) delta 7.81?7.90 (m, 8H), 7.75?7.77 (d, J = 10 Hz, 2H), 7.69?7.71 (d, J = 10 Hz, 2H),7.63?7.65 (d, J = 10 Hz, 2H), 7.56?7.58 (d, J = 10 Hz, 2H), 7.40?7.48 (m, 6H), 7.24?7.35 (m, 18H), 7.07?7.10(t, J = 11 Hz, 2H), 6.96?6.98 (d, J = 10 Hz, 4H), 6.88 (s, 2H), 6.78?6.80 (d, J = 10 Hz, 2H); 13C-NMR(CDCl3) delta 117.9, 120.0, 120.2, 122.0, 122.1, 122.9, 124.2, 124.3, 124.4, 126.2, 126.3, 126.4, 126.5, 126.6, 126.7,126.9, 127.2, 127.5, 127.7, 127.9, 128.4, 128.8, 129.6, 131.1, 134.3, 134.4, 135.3, 140.2, 140.3, 141.8, 143.4,145.9, 147.6, 149.8; GC-MS: 1003.05 for C77H50N2 [M + H+].
  • 3
  • [ 1232101-98-2 ]
  • [ 57103-20-5 ]
  • C70H47N3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% With tetrakis(triphenylphosphine) palladium(0); tri-tert-butyl phosphine; potassium carbonate; In toluene; at 110℃; for 48h; General procedure: A mixture of <strong>[57103-20-5]3,6-dibromo-9-phenyl-9H-carbazole</strong> 1 (1 g, 1 equiv), 4-(N-(naphthalen-2-yl)-N-(naphthalen-4-yl)amino)phenylboronic acid A(3.5 g, 3 equiv) or 9-(4-diphenylamino)phenyl)-9H-carbazol-2-yl-2-boronic acid B (4 g, 3.5 equiv), Pd(Ph3P)4 (0.8 g, 0.3 equiv), t-Bu3P 50%in toluene (0.15 ml, 0.6 equiv), K2CO3 (2 M, 50 ml) and 100 ml oftoluene were added then stirred under 110 C for 48 h. After completionof the reaction, the reaction mixtures were extracted with dichloromethaneand water. The organic layer was dried over anhydrousmagnesium sulphate then filtered and removed the solvent through rotary evaporation method. Crude residues were purified by silica gelcolumn chromatography by using n-hexane: dichloromethane solventsystem to achieve the requisite products 1A and 1B. 1AYield: 52%; yellow solid; 1H NMR (500 MHz, CDCl3) delta 8.38 (s, 2H),8.02-8.03 (d, J=5 Hz, 2H), 7.90-7.91 (d, J=5 Hz, 2H), 7.80-7.81 (d,J = 5 Hz, 2H), 7.68-7.73 (m, 4H), 7.43-7.60 (m, 22H), 7.33-7.36 (m,9H), 7.16-7.17 (d, J=5 Hz, 4H); 13C NMR (500 MHz, CDCl3) delta 147.28,146.22, 143.63, 140.56, 135.59, 135.42, 134.53, 133.93, 131.26,130.02, 129.61, 128.92, 128.53, 127.98, 127.64, 127.39, 127.02,126.96, 126.68, 126.62, 126.51, 126.36, 126.31, 125.32, 125.31,124.43, 124.16, 124.12, 123.00, 122.60, 118.40, 117.69, 110.21; GCMS:929.98 for C70H47N3 [M+H+]. Anal.calcd for C70H47N3 (%): C90.39, H 5.09, N 4.52; found C 89.76, H 5.05, N 4.56.
 

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