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Chemical Structure| 131922-15-1 Chemical Structure| 131922-15-1

Structure of 131922-15-1

Chemical Structure| 131922-15-1

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Product Details of [ 131922-15-1 ]

CAS No. :131922-15-1
Formula : C10H8O4
M.W : 192.17
SMILES Code : OC(O)C(C1=CC2=CC=CC=C2O1)=O
MDL No. :MFCD05864644
InChI Key :JVZHUDOMODCNLO-UHFFFAOYSA-N
Pubchem ID :44118544

Safety of [ 131922-15-1 ]

Application In Synthesis of [ 131922-15-1 ]

* 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 [ 131922-15-1 ]

[ 131922-15-1 ] Synthesis Path-Downstream   1~14

  • 1
  • [ 1646-26-0 ]
  • [ 131922-15-1 ]
YieldReaction ConditionsOperation in experiment
With iodine; In dimethyl sulfoxide; at 100.0℃; General procedure: A mixture of acetophenone 1a (120 mg, 1.0 mmol), benzylamine 2a (160.7 mg, 1.5 mmol), and iodine (507.6 mg, 2.0 mmol) in DMSO (3 mL) was stirred at 100 C for 5 h. After disappearance of the reactant (monitored by TLC), and added 50 mL water to the mixture, then extracted with EtOAc three times (3 50 mL). The extract was washed with 10% Na2S2O3 solution (w/w), dried over anhydrous Na2SO4 and evaporation. The residue was purified by column chromatography on silica gel (petroleum ether/EtOAc=100:1) to yield the desired product 3aa as a white solid (183.4 mg, 83% yield).
  • 3
  • [ 131922-15-1 ]
  • C19H14F3N3O3 [ No CAS ]
  • C19H14F3NO3 [ No CAS ]
  • C19H14F3NO3 [ No CAS ]
  • 4
  • [ 131922-15-1 ]
  • [ 1400693-93-7 ]
  • C19H14F3NO3 [ No CAS ]
  • C19H14F3N3O3 [ No CAS ]
  • 5
  • [ 131922-15-1 ]
  • [ 104-94-9 ]
  • C17H13NO4 [ No CAS ]
  • 6
  • [ 131922-15-1 ]
  • [ 100-46-9 ]
  • [ 1256602-69-3 ]
YieldReaction ConditionsOperation in experiment
With iodine; In dimethyl sulfoxide; at 100.0℃; 4.3.13 5-(Benzofuran-2-yl)-2-phenyloxazole (3ma) 11b Yield 72%; White solid; mp 140-143 C; IR (KBr): 3063, 2924, 1545, 1445, 1254, 1161, 1128, 1062, 879, 838, 789, 745, 703 cm-1; 1H NMR (400 MHz, CDCl3): delta (ppm) 8.15-8.08 (m, 2H), 7.61 (d, J=7.6 Hz, 1H), 7.57 (s, 1H), 7.54-7.45 (m, 4H), 7.33 (t, J=7.6 Hz, 1H), 7.29-7.22 (m, 1H), 7.05 (s, 1H); 13C NMR (100 MHz, CDCl3) delta (ppm) 161.7, 154.8, 145.2, 143.4, 130.7, 128.9, 128.3, 126.9, 126.5, 125.6, 125.1, 123.4, 121.2, 111.2, 103.2; HRMS (APCI): m/z [M+H]+ calcd for C17H12NO2: 262.0863; found: 262.0865.
  • 7
  • [ 131922-15-1 ]
  • [ 137-07-5 ]
  • C16H11NO2S [ No CAS ]
  • 8
  • [ 131922-15-1 ]
  • [ 75-64-9 ]
  • C20H21NO2 [ No CAS ]
  • 9
  • [ 131922-15-1 ]
  • [ 100-52-7 ]
  • benzofuran-2-yl(4,5-diphenyl-1H-pyrazol-3-yl)methanone [ No CAS ]
  • 10
  • [ 131922-15-1 ]
  • [ 123-54-6 ]
  • 1-(3-(benzofuran-2-carbonyl)-4-methyl-1H-pyrazol-5-yl)ethanone [ No CAS ]
  • 11
  • [ 95-20-5 ]
  • [ 131922-15-1 ]
  • [ 126-81-8 ]
  • C27H23NO4 [ No CAS ]
  • 12
  • [ 131922-15-1 ]
  • [ 438226-94-9 ]
YieldReaction ConditionsOperation in experiment
89% With caesium carbonate; toluene-4-sulfonic acid hydrazide; In chloroform; at 20.0℃; for 0.08333330000000001h; General procedure: 4.2. General procedure for synthesis of 3 (3a as an example) A reaction mixture of phenylglyoxal monohydrate 1a (152.2 mg,1.0 mmol), tosylhydrazine 2 (186.2 mg, 1.0 mmol), and Cs2CO3(977.4 mg, 3.0 mmol) in CHCl3 (2 mL) was stirred at room tem-perature for 5 min. Water (50 mL) was then added to the mixture.The organic layer was separated and the aqueous layer wasextracted with EtOAc (50 mL3). The product was dried over an-hydrous Na2SO4 and concentrated under reduced pressure. Theresidue was puried by column chromatography on silica gel (pe-troleum ether/EtOAc5/1) to afford the desired product 3a.
  • 13
  • [ 5344-90-1 ]
  • [ 131922-15-1 ]
  • C34H24N2O5 [ No CAS ]
YieldReaction ConditionsOperation in experiment
40% With trifluoroacetic acid; In methanol; at 60.0℃; for 1.0h;Sealed tube; 4.2 General procedure for synthesis of 3 (3a as an example).The mixture of phenylglyoxal monohydrate 1a (1.0mmol), 2-aminobenzylalcohol 2a (1.0mmol) was heated at 60C in 3mL of MeOH in a sealed vessel for 1h till almost completed conversion of the substrates monitored by TLC analysis. Then 50mL water was added to the mixture, which was extracted with EtOAc three times (3×50mL). The extract was dried over anhydrous Na2SO4 and concentrated in vacuo. The crude product was purified by column chromatography on silica gel (eluent: petroleum ether/EtOAc=15/1) to afford the product 3a. 4.3 Characterization data 4.3.1 Compound 3a Brown solid; mp 171-173C; 1H NMR (600MHz, CDCl3) delta 8.30 (d, J=7.8Hz, 2H), 7.65 (d, J=7.2Hz, 2H), 7.58 (t, J=7.2Hz, 1H), 7.44 (t, J=7.8Hz, 2H), 7.36-7.29 (m, 3H), 7.05 (t, J=7.8Hz, 1H), 7.00 (t, J=7.8Hz, 1H), 6.95 (t, J=7.8Hz, 1H), 6.92 (d, J=7.8Hz, 1H), 6.82-6.76 (m, 2H), 6.71 (t, J=7.2Hz, 1H), 6.51 (d, J=8.4Hz, 1H), 5.54 (s, 1H), 5.49 (s, 1H), 4.98 (d, J=14.4Hz, 1H), 4.92-4.87 (m, 2H), 4.59 (d, J=15.6Hz, 1H); 13C NMR (150MHz, CDCl3) delta 200.4, 139.10, 139.08, 136.7, 134.9, 133.4, 129.4, 128.7, 128.6, 128.4, 127.4, 126.2, 125.0, 124.0, 122.7, 120.4, 118.8, 112.3, 93.5, 91.9, 84.8, 68.3, 62.4; IR (KBr): 3056, 2944, 2854, 1973, 1681, 1598, 1499,1322, 1055, 754cm-1; HRMS (ESI): m/z [M+Na]+ calcd for C30H24N2NaO3: 483.1679; found: 483.1675.
40% With trifluoroacetic acid; In methanol; at 60.0℃; for 1.0h; General procedure: The mixture of phenylglyoxal monohydrate 1a (1.0 mmol), 2-aminobenzyl alcohol 2a (1.0 mmol) was heated at 60 C in 3 mL of MeOH in a sealed vessel for 1 h till almost completed conversion ofthe substrates monitored by TLC analysis. Then 50 mL water was added to the mixture, which was extracted with EtOAc three times (3*50 mL). The extract was dried over anhydrous Na2SO4 and concentrated in vacuo. The crude product was purified by column chromatography on silica gel (eluent: petroleum ether/EtOAc 15/1) to afford the product 3a.
  • 14
  • [ 95-20-5 ]
  • [ 533-31-3 ]
  • [ 131922-15-1 ]
  • 3-(6-(benzofuran-2-yl)-[1,3]dioxolo[4,5-f]benzofuran-7-yl)-2-methyl-1H-indole [ No CAS ]
 

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