65847-34-9

Basic information

• Product Name: Benzenamine, 4-(1-phenyl-1H-benzimidazol-2-yl)-
• CAS NO: 65847-34-9
• Molecular Formula: C19H15N3
• Molecular Weight: 285.348
• Mol File: 65847-34-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-(1-phenyl-1H-benzimidazol-2-yl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-(1-phenyl-1H-benzimidazol-2-yl)-(65847-34-9)
• EPA Substance Registry System: Benzenamine, 4-(1-phenyl-1H-benzimidazol-2-yl)-(65847-34-9)

Safety Data

• Hazardous Substances Data: 65847-34-9(Hazardous Substances Data)

Upstream product

• 729-13-5 2-(4-nitrophenyl)benzimidazole 
• 555-16-8 4-nitrobenzaldehdye 
• 95-54-5 1,2-diamino-benzene 
• 2620-76-0 2-(4-bromophenyl)-1-phenyl-1H-benzimidazole 
• 4403-71-8 (4-aminomethyl)aniline 
• 534-85-0 N-phenyl-1,2-benzenediamine 
• 122-04-3 4-nitro-benzoyl chloride 
• 65847-31-6 2-(4-nitrophenyl)-1-phenyl-1H-benzimidazole 

Relevant articles and documents

Organometallic compound, and organic light emitting diode and organic light emitting device including same

The present disclosure provides an organometallic compound shown in the specification, and an organic light emitting diode and an organic light emitting display device including the organometallic compound.

Tertiary amine derivatives and organic electroluminescent device including the same

Provided is a tertiary amine derivative which contributes to a substantial increase in service life of an organic electroluminescent device by minimizing damages to organic matter inside the organic electroluminescent device via effective absorption of a high-energy external light source in the UV region. According to the present invention, the organic electroluminescent device comprises: a first electrode and a second electrode; and one or more organic material layers disposed between the first electrode and the second electrode, wherein the organic material layers comprise a tertiary amine derivative represented by chemical formula 1. In the chemical formula 1, Z_1, Z_2, and Z_3 are each independently O or S.COPYRIGHT KIPO 2020

A Bioinspired Catalytic Aerobic Oxidative C-H Functionalization of Primary Aliphatic Amines: Synthesis of 1,2-Disubstituted Benzimidazoles

Aerobic oxidative C-H functionalization of primary aliphatic amines has been accomplished with a biomimetic cooperative catalytic system to furnish 1,2-disubstituted benzimidazoles that play an important role as drug discovery targets. This one-pot atom-economical multistep process, which proceeds under mild conditions, with ambient air and equimolar amounts of each coupling partner, constitutes a convenient environmentally friendly strategy to functionalize non-activated aliphatic amines that remain challenging substrates for non-enzymatic catalytic aerobic systems.