1441045-97-1

Basic information

• Product Name: (S)-[2-(methoxydiphenylmethyl)pyrrolidin-1-yl](1-methyl-1H-imidazol-2-yl)methanone
• Synonyms: (S)-[2-(methoxydiphenylmethyl)pyrrolidin-1-yl](1-methyl-1H-imidazol-2-yl)methanone
• CAS NO: 1441045-97-1
• Molecular Weight: 375.47
• Mol File: 1441045-97-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-[2-(methoxydiphenylmethyl)pyrrolidin-1-yl](1-methyl-1H-imidazol-2-yl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-[2-(methoxydiphenylmethyl)pyrrolidin-1-yl](1-methyl-1H-imidazol-2-yl)methanone(1441045-97-1)
• EPA Substance Registry System: (S)-[2-(methoxydiphenylmethyl)pyrrolidin-1-yl](1-methyl-1H-imidazol-2-yl)methanone(1441045-97-1)

Safety Data

• Hazardous Substances Data: 1441045-97-1(Hazardous Substances Data)

Upstream product

• 1111092-50-2 [(S)-2-(hydroxydiphenylmethyl)-pyrrolidin-1-yl]-(1-methyl-1H-imidazol-2-yl)methanone 
• 74-88-4 methyl iodide 
• 30148-21-1 ethyl 1-methyl-1H-imidazole-2-carboxylate 
• 22348-32-9 (S)-diphenylprolinol 

Relevant articles and documents

Mechanistic investigations of the asymmetric hydrosilylation of ketimines with trichlorosilane reveals a dual activation model and an organocatalyst with enhanced efficiency

Structural probes used to help elucidate mechanistic information of the organocatalyzed asymmetric ketimine hydrosilylation have revealed a new catalyst with unprecedented catalytic activity, maintaining adequate performance at 0.01 mol% loading. A new ‘dual activation’ model has been proposed that relies on the presence of both a Lewis basic and Br?nsted acidic site within the catalyst architecture.