1352335-19-3

Basic information

• Product Name: (S)-2-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-methylpropanal
• Synonyms: (S)-2-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-methylpropanal
• CAS NO: 1352335-19-3
• Molecular Weight: 324.174
• Mol File: 1352335-19-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (S)-2-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-methylpropanal(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-methylpropanal(1352335-19-3)
• EPA Substance Registry System: (S)-2-(1-(3-bromophenyl)-2,5-dioxopyrrolidin-3-yl)-2-methylpropanal(1352335-19-3)

Safety Data

• Hazardous Substances Data: 1352335-19-3(Hazardous Substances Data)

Upstream product

• 53534-14-8 N-(3-bromophenyl)maleimide 
• 78-84-2 isobutyraldehyde 

Relevant articles and documents

Highly enantioselective Michael addition of α,α-disubstituted aldehydes to maleimides catalyzed by new primary amine-squaramide bifunctional organocatalysts

New bifunctional primary amine-squaramides catalyzed asymmetric Michael addition reaction of α,α-disubstituted aldehydes to maleimides has been developed. This organocatalytic asymmetric reaction provides easy access to functionalized succinimides with a

A highly efficient large-scale asymmetric Michael addition of isobutyraldehyde to maleimides promoted by a novel multifunctional thiourea

A novel class of chiral multifunctional thioureas bearing a chiral lipophilic beyerane scaffold and a primary amino group were designed and prepared. The thioureas were proven to be effective for catalyzing the asymmetric Michael addition between isobutyr