399559-57-0

Basic information

• Product Name: 1-Pyrrolidinecarboxylic acid, 2-[(1R)-1-hydroxy-3-[(R)-(4-methylphenyl)sulfinyl]-3-butenyl]-, 1,1-dimethylethyl ester, (2S)-
• CAS NO: 399559-57-0
• Molecular Formula: C20H29NO4S
• Molecular Weight: 379.521
• Mol File: 399559-57-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-Pyrrolidinecarboxylic acid, 2-[(1R)-1-hydroxy-3-[(R)-(4-methylphenyl)sulfinyl]-3-butenyl]-, 1,1-dimethylethyl ester, (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1-Pyrrolidinecarboxylic acid, 2-[(1R)-1-hydroxy-3-[(R)-(4-methylphenyl)sulfinyl]-3-butenyl]-, 1,1-dimethylethyl ester, (2S)-(399559-57-0)
• EPA Substance Registry System: 1-Pyrrolidinecarboxylic acid, 2-[(1R)-1-hydroxy-3-[(R)-(4-methylphenyl)sulfinyl]-3-butenyl]-, 1,1-dimethylethyl ester, (2S)-(399559-57-0)

Safety Data

• Hazardous Substances Data: 399559-57-0(Hazardous Substances Data)

Upstream product

• 73365-02-3 tert-butoxycarbonyl-D-prolinal 
• 261900-93-0 (S_S)-(+)-3-chloro-2-(p-tolylsulfinyl)prop-2-ene 

Relevant articles and documents

Barbier-type diastereoselective allylation of α-amino aldehydes with an enantiopure 2-sulfinylallyl building block

An optimized procedure for the diastereoselective allylation under aqueous Barbier conditions of a series of α-amino aldehydes with our new chiral building block (Ss)-3-chloro-2-(p-tolylsulfinyl)-1-propene [(Ss)-1a] to afford enantiomerically pure sulfinylamino alcohols in good yields and diastereoselectivites is reported. High levels of diastereoinduction can be achieved from α-amino aldehydes configurationally related to natural α-amino acids.