1572-03-8

Basic information

• Product Name: 2-(3-chlorophenyl)-1H-benzo[d]imidazol-5-amine
• Synonyms: 2-(3-chlorophenyl)-1H-benzo[d]imidazol-5-amine
• CAS NO: 1572-03-8
• Molecular Weight: 243.695
• Mol File: 1572-03-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-(3-chlorophenyl)-1H-benzo[d]imidazol-5-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-chlorophenyl)-1H-benzo[d]imidazol-5-amine(1572-03-8)
• EPA Substance Registry System: 2-(3-chlorophenyl)-1H-benzo[d]imidazol-5-amine(1572-03-8)

Safety Data

• Hazardous Substances Data: 1572-03-8(Hazardous Substances Data)

Upstream product

• 1571-88-6 2-(3-chlorophenyl)-5-nitro-1H-benzo[d]imidazole 
• 535-80-8 3-chlorobenzoate 
• 99-56-9 4-Nitrophenylene-1,2-diamine 

Downstream Products

• 1593834-62-8 N-(2-(3-chlorophenyl)-1H-benzo[d]imidazol-6-yl)quinolin-4-amine 

Relevant articles and documents

COMPOUNDS FOR TREATING TUBERCULOSIS

The invention concerns a compound of formula (Ia) or (Ib) wherein R1 is hydrogen or a methyl group; R2 is an unsubstituted or substituted alkyl group; R3 is an aryl group or a heteroaryl group, optionally substituted by on

Discovery of quinazolin-4-amines bearing benzimidazole fragments as dual inhibitors of c-Met and VEGFR-2

Both c-Met and VEGFR-2 are important targets for the treatment of cancers. In this study, a series of N-(2-phenyl-1H-benzo[d]imidazol-5-yl)quinazolin-4- amine derivatives were designed and identified as dual c-Met and VEGFR-2 inhibitors. Among these compounds bearing quinazoline and benzimidazole fragments, compound 7j exhibited the most potent inhibitory activity against c-Met and VEGFR-2 with IC50 of 0.05 μM and 0.02 μM, respectively. It also showed the highest anticancer activity against the tested cancer cell lines with IC50 of 1.5 μM against MCF-7 and 8.7 μM against Hep-G2. Docking simulation supported the initial pharmacophoric hypothesis and suggested a common mode of interaction at the ATP-binding site of c-Met and VEGFR-2, which demonstrates that compound 7j is a potential agent for cancer therapy deserving further researching.