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1-(4-Bromophenyl)-2-phenylbenzimidazole

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1-(4-Bromophenyl)-2-phenylbenzimidazole Basic information

Product Name:
1-(4-Bromophenyl)-2-phenylbenzimidazole
Synonyms:
  • 1H-BenziMidazole, 1-(4-broMophenyl)-2-phenyl
  • 1-(4-broMophenyl)-2-phenyl-1H-benzo[d]iMidazole
  • 1-(4-BroMo-phenyl)-2-phenyl-1H-benzoiMidazole
  • 1-(4-Bromophenyl)-2-phenyl-1H-benzimidazole
  • 1-(4-bromophenyl)-2-phenyl-1H-benzo[d]imidazole1
  • 1-(4-Bromophenyl)-2-phenyl-1H-1,3-benzodiazole
  • 1-(4-Bromophenyl)-2-phenylbenzimidazole
  • 2-1H-BenziMidazole, 1-(4-broMophenyl)-2-phenyl
CAS:
760212-58-6
MF:
C19H13BrN2
MW:
349.22
EINECS:
208-028-7
Product Categories:
  • OLED
Mol File:
760212-58-6.mol
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1-(4-Bromophenyl)-2-phenylbenzimidazole Chemical Properties

Melting point:
135.0 to 139.0 °C
Boiling point:
503.5±52.0 °C(Predicted)
Density 
1.38±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
pka
3.85±0.10(Predicted)
color 
White to Light yellow to Light orange
InChI
InChI=1S/C19H13BrN2/c20-15-10-12-16(13-11-15)22-18-9-5-4-8-17(18)21-19(22)14-6-2-1-3-7-14/h1-13H
InChIKey
PPYIZNYOMNYZCG-UHFFFAOYSA-N
SMILES
C1(C2=CC=CC=C2)N(C2=CC=C(Br)C=C2)C2=CC=CC=C2N=1
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Safety Information

HS Code 
2933.99.8290
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1-(4-Bromophenyl)-2-phenylbenzimidazole Usage And Synthesis

Uses

1-(4-bromophenyl)-2-phenyl-1H-benzo[d]imidazole is a useful research chemical.

Uses

1-(4-Bromophenyl)-2-phenylbenzimidazole is a phosphorescent organic semiconductor. It can be used in devices such as light emitting diodes and organic solar cells, which are based on the electroluminescence of materials that emit light when electrically stimulated. 1-(4-Bromophenyl)-2-phenylbenzimidazole has been shown to exhibit efficient electron and ionic transport properties, both in cyclic voltammetry and in thin film transistors.

Synthesis

1-(4-Bromophenyl)-2-phenylbenzimidazole can be synthesized using tert-butylchloroformate, benzaldehyde, and 4-bromobenzaldehyde in a cyclic reaction with potassium tert-butoxide as the catalyst. The product is purified by recrystallization from acetone.

References

[1] Patent: US9548460, 2017, B2. Location in patent: Page/Page column 80; 82
[2] Patent: EP1734038, 2006, A1. Location in patent: Page/Page column 47
[3] Patent: EP1602648, 2005, A1. Location in patent: Page/Page column 36
[4] Patent: EP2524913, 2012, A1. Location in patent: Page/Page column 31
[5] Patent: EP2530071, 2012, A1. Location in patent: Page/Page column 28-29

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