1431769-22-0

Basic information

• Product Name: (S)-tert-butyl 2-{[2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-methylpropanoyl]carbamoyl}-3-methylbutanoate
• Synonyms: (S)-tert-butyl 2-{[2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-methylpropanoyl]carbamoyl}-3-methylbutanoate
• CAS NO: 1431769-22-0
• Molecular Weight: 416.517
• Mol File: 1431769-22-0.mol

Chemical Properties

• CAS DataBase Reference: (S)-tert-butyl 2-{[2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-methylpropanoyl]carbamoyl}-3-methylbutanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-tert-butyl 2-{[2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-methylpropanoyl]carbamoyl}-3-methylbutanoate(1431769-22-0)
• EPA Substance Registry System: (S)-tert-butyl 2-{[2-((S)-2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-methylpropanoyl]carbamoyl}-3-methylbutanoate(1431769-22-0)

Safety Data

• Hazardous Substances Data: 1431769-22-0(Hazardous Substances Data)

Upstream product

• 1242461-29-5 (S)-2-(2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-methylpropionaldehyde 
• 941-69-5 N-phenyl-maleimide 
• 1431769-80-0 (S)-2-(2,5-dioxo-1-phenylpyrrolidin-3-yl)-2-methylpropanoic acid 
• 13518-40-6 L-valine tert-butylester hydrochloride 

Relevant articles and documents

An asymmetric Michael addition of α,α-disubstituted aldehydes to maleimides leading to a one-pot enantioselective synthesis of lactones catalyzed by amino acids

A cheap and fast construction of both enantiomers of substituted succinimides is reported. α- or β-amino acids, such as β-phenylalanine and α-tert-butyl aspartate, were found to be efficient organocatalysts for the reaction between α,α-disubstituted aldeh