134856-47-6

Basic information

• Product Name: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-4-methyl- (9CI)
• Synonyms: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-4-methyl- (9CI)
• CAS NO: 134856-47-6
• Molecular Formula: C12H14N2
• Molecular Weight: 186.25296
• Product Categories: BENZIMIDAZOLE
• Mol File: 134856-47-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-4-methyl- (9CI)(CAS DataBase Reference)
• NIST Chemistry Reference: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-4-methyl- (9CI)(134856-47-6)
• EPA Substance Registry System: Pyrido[1,2-a]benzimidazole, 1,2,3,4-tetrahydro-4-methyl- (9CI)(134856-47-6)

Safety Data

• Hazardous Substances Data: 134856-47-6(Hazardous Substances Data)

Upstream product

• 821-09-0 n-Pent-4-enyl alcohol 
• 64818-35-5 4-pentenyl mesylate 
• 1374668-49-1 1-(pent-4-en-1-yl)-1H-benzo[d]imidazole 
• 134856-53-4 N-(pent-4-enyl)-2-nitrobenzenamine 
• 88-73-3 2-Chloronitrobenzene 
• 22537-07-1 4-pentenyl-1-amine 
• 201230-82-2 carbon monoxide 
• 134856-37-4 N-(pent-4-enyl)benzene-1,2-diamine 

Relevant articles and documents

Construction of All-Carbon Quaternary Stereocenters by Scandium-Catalyzed Intramolecular C-H Alkylation of Imidazoles with 1,1-Disubstituted Alkenes

The exo-selective C-H cycloaddition of imidazoles to 1,1-disubstituted alkenes has been achieved for the first time by using half-sandwich scandium catalysts. A wide range of imidazole compounds bearing various 1,1-disubstituted aliphatic alkenes, styrenes, dienes, and enynes have been selectively converted in high yields to the corresponding bicyclic imidazole derivatives bearing β-all-carbon-substituted quaternary stereocenters. By using a chiral half-sandwich scandium catalyst, the asymmetric exo-selective cyclization has also been achieved with a high level of enantioselectivity.

A metal catalysed route to benzimidazoles containing a fused alicyclic ring

Rhodium catalysed reactions of N-alkenyl-1,2-diaminobenzenes (1) with hydrogen and carbon monoxide give benzimidazoles containing a fused alicyclic ring (6,7) in excellent yields.