2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole

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CAS:2620-76-0
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2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole manufacturers

2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole Basic information
Uses
Product Name:2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole
Synonyms:2-(4-BROMO-PHENYL)-1-PHENYL-1H-BENZOIMIDAZOLE;2-(4-broMophenyl)-1-phenyl-1H-1,3-benzodiazole;2-(4-BroMophenyl)-1-phenylbenziMidazole;BIBA-A;1H-Benzimidazole,2-(4-bromophenyl)-1-phenyl-;2-(4-broMophenyl)-1-phenyl-1H-benzo[d]iMidazole;2-(4-BroMophenyl)-1-phenylbenzoiMidazole, 97%;2-(4-Bromophenyl)-1-phenylbenzimidazole >
CAS:2620-76-0
MF:C19H13BrN2
MW:349.22
EINECS:1533716-785-6
Product Categories:OLED materials,pharm chemical,electronic;OLED
Mol File:2620-76-0.mol
2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole Structure
2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole Chemical Properties
Melting point 162-166℃
Boiling point 503.5±52.0 °C(Predicted)
density 1.38±0.1 g/cm3(Predicted)
storage temp. Inert atmosphere,Room Temperature
form Powder
pka3.75±0.10(Predicted)
color Off-white
λmax297nm(CH3CN)(lit.)
InChIInChI=1S/C19H13BrN2/c20-15-12-10-14(11-13-15)19-21-17-8-4-5-9-18(17)22(19)16-6-2-1-3-7-16/h1-13H
InChIKeyDXRLALXPCIOIDK-UHFFFAOYSA-N
SMILESC1(C2=CC=C(Br)C=C2)N(C2=CC=CC=C2)C2=CC=CC=C2N=1
CAS DataBase Reference2620-76-0
Safety Information
HS Code 2934999090
MSDS Information
2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole Usage And Synthesis
Uses2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole is a useful research chemical.
Chemical PropertiesWhite to yellow Crystal
Synthesis
4-Bromo-N-(2-(phenylamino)phenyl)benzamide

359427-13-7

2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole

2620-76-0

General procedure for the synthesis of 1-phenyl-2-(4-bromophenyl)-1H-benzimidazole from the compound (CAS:359427-13-7): Example 1.3.2; 9; Synthesis of 2-(4-bromophenyl)-1-phenyl-1H-benzo[d]imidazole (9): amide 1 (9.6 g, 26 mmol) was suspended in anhydrous 1,4-dioxane (100 mL), and phosphorus oxychloride (POCl3) (9.2 mL, 100 mmol) was slowly added. Subsequently, the reaction mixture was heated at 100 °C overnight. After completion of the reaction, it was cooled to room temperature and the mixture was slowly poured into ice (200 g) under stirring. The precipitate was collected by filtration and recrystallized in dichloromethane (DCM)/hexane solvent mixture to give a light gray solid product (compound 9) (8.2 g, 90% yield).

References[1] Advanced Functional Materials, 2010, vol. 20, # 3, p. 399 - 408
[2] Journal of Materials Chemistry, 2012, vol. 22, # 43, p. 23005 - 23011
[3] Journal of Materials Chemistry C, 2013, vol. 1, # 11, p. 2217 - 2223
[4] Patent: WO2011/8560, 2011, A1. Location in patent: Page/Page column 30
[5] Patent: WO2011/34967, 2011, A1. Location in patent: Page/Page column 22
Tag:2-(4-Bromophenyl)-1-phenyl-1H-benzoimidazole(2620-76-0) Related Product Information
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