31413-80-6

Basic information

• Product Name: 1H-Benzimidazol-2-amine, N,1-diphenyl-
• CAS NO: 31413-80-6
• Molecular Formula: C19H15N3
• Molecular Weight: 285.348
• Mol File: 31413-80-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1H-Benzimidazol-2-amine, N,1-diphenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazol-2-amine, N,1-diphenyl-(31413-80-6)
• EPA Substance Registry System: 1H-Benzimidazol-2-amine, N,1-diphenyl-(31413-80-6)

Safety Data

• Hazardous Substances Data: 31413-80-6(Hazardous Substances Data)

Upstream product

• 102-06-7 diphenylguanidine 
• 583-53-9 2,3-dibromobenzene 
• 101-01-9 N,N',N''-triphenylguanidine 
• 2622-60-8 1-phenyl-1H-benzoimidazole 
• 62-53-3 aniline 
• 1397718-84-1 N-(2-iodophenyl) carbonimidoyl dichloride 
• 1397718-81-8 N-(2-bromophenyl) carbonimidoyl dichloride 
• 622-16-2 1,3-Diphenylcarbodiimide 
• 615-36-1 2-bromoaniline 
• 615-43-0 2-iodophenylamine 

Downstream Products

• 1242169-15-8 C₃₃H₂₄ClN₅ 

Relevant articles and documents

Oxidant-switchable selective synthesis of 2-aminobenzimidazoles via c-h amination/acetoxylation of guanidines

The iodine(III) compound promoted C-H amination and tandem C-H amination/acetoxylation of guanidines are achieved for the first time to provide efficiently 2-aminobenzimidazoles and acetoxyl-substituted 2-aminobenzimidazoles, respectively. The amount and

Eco-friendly strategy: design and synthesis of biologically potent benzimidazole-amine hybrids via visible-light generated oxidative C-H arylamylation of analenic amidines

An operationally simple visible light mediated intramolecular cyclization of benzimidazole to 2-amino benzimidazole hybrid. The disclosed procedure is rapid and the convenient synthesis of benzimidazole-amine hybrids from easily available substituted cycl

A protocol to 2-aminobenzimidazoles via copper-catalyzed cascade addition and cyclization of o-haloanilines and carbodiimides

An efficient strategy for the synthesis of a variety of 2-animobenzimidazole derivatives has been developed. The reaction proceeded from o-haloanilines and carbodiimides via copper(I)-catalyzed domino reaction in the presence of tert-butoxide to afford the corresponding 2-animobenzimidazole derivatives in good to excellent yields. o-Haloanilines could be o-iodoaniline, o-bromoaniline, and o-chloroaniline derivatives. Carbodiimides could be symmetrical and unsymmetrical substrates with aryl or alkyl substituents. The reaction exhibited a good regioselectivity when unsymmetrical carbodiimides were employed.