1095532-20-9

Basic information

• Product Name: (2R,3R)-2-(benzylthio)-3-(3-chlorophenyl)-3-(2,5-dioxopyrrolidin-1-yl)propanal
• Synonyms: (2R,3R)-2-(benzylthio)-3-(3-chlorophenyl)-3-(2,5-dioxopyrrolidin-1-yl)propanal
• CAS NO: 1095532-20-9
• Molecular Weight: 387.887
• Mol File: 1095532-20-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2R,3R)-2-(benzylthio)-3-(3-chlorophenyl)-3-(2,5-dioxopyrrolidin-1-yl)propanal(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,3R)-2-(benzylthio)-3-(3-chlorophenyl)-3-(2,5-dioxopyrrolidin-1-yl)propanal(1095532-20-9)
• EPA Substance Registry System: (2R,3R)-2-(benzylthio)-3-(3-chlorophenyl)-3-(2,5-dioxopyrrolidin-1-yl)propanal(1095532-20-9)

Safety Data

• Hazardous Substances Data: 1095532-20-9(Hazardous Substances Data)

Upstream product

• 56578-37-1 3-(3-chlorophenyl)acrylaldehyde 
• 14204-23-0 N-(benzylthio)succinimide 

Relevant articles and documents

Organocatalytic enantioselective aminosulfenylation of α,β- unsaturated aldehydes

(Chemical Equation Presented) Domino theory: A simple, highly enantioselective organocatalytic aminosulfenylation of α,β- unsaturated aldehydes affords orthogonally protected β-amino-α- mercaptoaldehydes in high yields and 93 to >99% ee (see scheme, Bn=benzyl). Notably, the catalytic transformation shows that it is possible to efficiently employ all components of an electrophile, which includes a nucleofuge, in organocatalytic domino reactions of enals.