1261527-54-1

Basic information

• Product Name: 6-methyl-2-(piperidin-1-yl)-1-(p-tolyl)-1H-benzo[d]imidazole
• Synonyms: 6-methyl-2-(piperidin-1-yl)-1-(p-tolyl)-1H-benzo[d]imidazole
• CAS NO: 1261527-54-1
• Molecular Weight: 305.423
• Mol File: 1261527-54-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-methyl-2-(piperidin-1-yl)-1-(p-tolyl)-1H-benzo[d]imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 6-methyl-2-(piperidin-1-yl)-1-(p-tolyl)-1H-benzo[d]imidazole(1261527-54-1)
• EPA Substance Registry System: 6-methyl-2-(piperidin-1-yl)-1-(p-tolyl)-1H-benzo[d]imidazole(1261527-54-1)

Safety Data

• Hazardous Substances Data: 1261527-54-1(Hazardous Substances Data)

Upstream product

• 106-49-0 p-toluidine 
• 110-89-4 piperidine 
• 5720-05-8 4-methylphenylboronic acid 
• 10532-64-6 N-(4-methylphenyl)cyanamide 
• 726-42-1 di-p-tolylcarbodiimide 

Relevant articles and documents

Copper-Catalyzed Domino Three-Component Approach for the Assembly of 2-Aminated Benzimidazoles and Quinazolines

A copper-promoted three-component synthesis of 2-aminobenzimidazoles (1) or of 2-aminoquinazolines (2) involving cyanamides, arylboronic acids, and amines has been developed. The operationally simple oxidative process, performed in the presence of K2

Copper(II) acetate/oxygen-mediated nucleophilic addition and intramolecular C-H activation/C-N or C-C bond formation: One-pot synthesis of benzimidazoles or quinazolines

Diarylcarbodiimides or benzylphenylcarbodiimides are converted to 1,2-disubstituted benzimidazoles or 1,2-disustituted quinazolines via addition/intramolecular C-H bond activation/C-N or C-C bond forming reaction using copper(II) acetate/oxygen [Cu(OAc)2/O2] as the oxidant at 100°C in one-pot cascade procedure. Copyright