634193-92-3

Basic information

• Product Name: 1H-Benzimidazole, 1-[(3,5-dimethylphenyl)methyl]-2-[(1-methylethyl)sulfonyl]-
• CAS NO: 634193-92-3
• Molecular Formula: C19H22N2O2S
• Molecular Weight: 342.462
• Mol File: 634193-92-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1H-Benzimidazole, 1-[(3,5-dimethylphenyl)methyl]-2-[(1-methylethyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazole, 1-[(3,5-dimethylphenyl)methyl]-2-[(1-methylethyl)sulfonyl]-(634193-92-3)
• EPA Substance Registry System: 1H-Benzimidazole, 1-[(3,5-dimethylphenyl)methyl]-2-[(1-methylethyl)sulfonyl]-(634193-92-3)

Safety Data

• Hazardous Substances Data: 634193-92-3(Hazardous Substances Data)

Upstream product

• 27129-86-8 1-bromomethyl-3,5-dimethylbenzene 
• 124530-70-7 2-(1-methylthio)benzimidazole 
• 634193-85-4 1-[(3,5-dimethylphenyl)methyl]-2-[(1-methylethyl)thio]benzimidazole 

Downstream Products

• 634194-03-9 1-[(3,5-dimethylphenyl)methyl]-2-[(1-methylethenyl)sulfonyl]benzimidazole 

Relevant articles and documents

Enantioselective hydrogen atom transfer to α-sulfonyl radicals controlled by selective coordination of a chiral Lewis acid to an enantiotopic sulfonyl oxygen

Enantioselective hydrogen atom transfer to α-sulfonyl radicals generated from the alkyl radical addition to 2-propenyl and 1-phenylethenyl sulfones in the presence of chiral Lewis acids affords products with high enantioselectivity. The stereochemical course is discussed with the transition states involving selective coordination of a chiral Lewis acid to an enantiotopic sulfonyl oxygen.