615579-75-4

Basic information

• Product Name: (3S)-3-[(4R)-2-oxo-4-phenyl-1,3-oxazolan-3-yl]pentanoic acid
• Synonyms: (3S)-3-[(4R)-2-oxo-4-phenyl-1,3-oxazolan-3-yl]pentanoic acid
• CAS NO: 615579-75-4
• Molecular Weight: 263.293
• Mol File: 615579-75-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (3S)-3-[(4R)-2-oxo-4-phenyl-1,3-oxazolan-3-yl]pentanoic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (3S)-3-[(4R)-2-oxo-4-phenyl-1,3-oxazolan-3-yl]pentanoic acid(615579-75-4)
• EPA Substance Registry System: (3S)-3-[(4R)-2-oxo-4-phenyl-1,3-oxazolan-3-yl]pentanoic acid(615579-75-4)

Safety Data

• Hazardous Substances Data: 615579-75-4(Hazardous Substances Data)

Upstream product

• 615579-48-1 (4R)-4-phenyl-3-(1S)-1-[(trimethylsilyl)oxy]propyl-1,3-oxazolan-2-one 
• 160695-26-1 (4R)-3-propionyl-4-phenyl-1,3-oxazolidin-2-one 
• 615579-62-9 ethyl (3S)-3-[(4R)-2-oxo-4-phenyl-1,3-oxazolan-3-yl]pentanoate 

Downstream Products

• 271600-24-9 (3S)-3-({[(phenylmethyl)oxy]carbonyl}amino)pentanoic acid 

Relevant articles and documents

Stereoselective formation of N-acyliminium ion via chiral N,O-acetal TMS ether and its application to the synthesis of β-amino acids

(Matrix Presented) The highly stereoselective synthesis of β-amino acids via the chiral 4-phenyloxazolidinone-controlled linear N-acyliminium ion reaction has been achieved by employing chiral N,O-acetal TMS ethers. In addition, the mechanism of the excel