1441063-84-8

Basic information

• Product Name: (S,E)-4-benzyl-3-(3-oxobut-1-en-1-yl)oxazolidin-2-one
• Synonyms: (S,E)-4-benzyl-3-(3-oxobut-1-en-1-yl)oxazolidin-2-one
• CAS NO: 1441063-84-8
• Molecular Weight: 245.278
• Mol File: 1441063-84-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S,E)-4-benzyl-3-(3-oxobut-1-en-1-yl)oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S,E)-4-benzyl-3-(3-oxobut-1-en-1-yl)oxazolidin-2-one(1441063-84-8)
• EPA Substance Registry System: (S,E)-4-benzyl-3-(3-oxobut-1-en-1-yl)oxazolidin-2-one(1441063-84-8)

Safety Data

• Hazardous Substances Data: 1441063-84-8(Hazardous Substances Data)

Upstream product

• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 
• 1423-60-5 methyl ethynyl ketone 
• 1333419-28-5 (S)-4-benzyl-3-[(E)-2-(methoxycarbonyl)vinyl]-1,3-oxazolidin-2-one 

Downstream Products

• 1333419-28-5 (S)-4-benzyl-3-[(E)-2-(methoxycarbonyl)vinyl]-1,3-oxazolidin-2-one 
• 90719-32-7 (S)-4-Benzyl-2-oxazolidinone 

Relevant articles and documents

Diastereoselective synthesis of β-amino ketone and acid derivatives by palladium-catalyzed conjugate addition

The first diastereoselective synthesis of β-amino ketone and β-amino acid derivatives by palladium-catalyzed conjugate addition of arylboronic acids to chiral β-enamino ketones and β-enamino esters is reported. The catalytic system employing (S)-4-(tert-butyl)oxazolidin-2-one as the chiral auxiliary in water under an air atmosphere provides β-amino ketone and β-amino acid derivatives in high yields with excellent diastereoselectivity.