212385-56-3

Basic information

• Product Name: Benzenamine, 4-(9H-carbazol-9-yl)-N,N-diphenyl-
• CAS NO: 212385-56-3
• Molecular Formula: C30H22N2
• Molecular Weight: 410.518
• Mol File: 212385-56-3.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, 4-(9H-carbazol-9-yl)-N,N-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, 4-(9H-carbazol-9-yl)-N,N-diphenyl-(212385-56-3)
• EPA Substance Registry System: Benzenamine, 4-(9H-carbazol-9-yl)-N,N-diphenyl-(212385-56-3)

Safety Data

• Hazardous Substances Data: 212385-56-3(Hazardous Substances Data)

Upstream product

• 36809-26-4 4-N,N-diphenylamino-1-bromobenzene 
• 74367-40-1 N-(trimethylsilyl)-9H-carbazole 
• 16982-76-6 9-(4-nitrophenyl)-9H-carbazole 
• 122-39-4 diphenylamine 
• 86-74-8 9H-carbazole 
• 350-46-9 4-Fluoronitrobenzene 
• 591-50-4 iodobenzene 
• 52708-37-9 4-(9H-carbazol-9-yl)aniline 

Relevant articles and documents

Nickel-Catalyzed N-Arylation Using N -Trimethylsilyl-carbazole

Nickel-catalyzed N-arylation reaction of N -trimethylsilyl-carbazole using aryl bromides is found to proceed in the presence of sodium acetate, giving N -aryl-carbazoles in high yields. Under these conditions, N -trimethylsilyl-carbazole could react with aryl bromides selectively even in the presence of other N -trimethylsilyl-amines or N -H-amines. This arylation reaction was applied to the polymerization to provide a polycarbazole.

Electrochemically fabricated electrochromic films from 4-(: N -carbazolyl)triphenylamine and its dimethoxy derivative

A carbazolyl-substituted triphenylamine derivative, 4-(N-carbazolyl)triphenylamine (TPACz), was synthesized and used to build a fluorescent and electrochromic polymeric film (PTPACz) on the ITO-glass surface by electrochemical oxidative coupling reactions