96735-60-3

Basic information

• Product Name: Formic acid (R)-1-[(S)-2-oxo-4-((E)-styryl)-azetidin-3-yl]-ethyl ester
• CAS NO: 96735-60-3
• Molecular Weight: 245.278
• Mol File: 96735-60-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Formic acid (R)-1-[(S)-2-oxo-4-((E)-styryl)-azetidin-3-yl]-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Formic acid (R)-1-[(S)-2-oxo-4-((E)-styryl)-azetidin-3-yl]-ethyl ester(96735-60-3)
• EPA Substance Registry System: Formic acid (R)-1-[(S)-2-oxo-4-((E)-styryl)-azetidin-3-yl]-ethyl ester(96735-60-3)

Safety Data

• Hazardous Substances Data: 96735-60-3(Hazardous Substances Data)

Upstream product

• 64-18-6 formic acid 
• 96735-59-0 (S)-3-((S)-1-Hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one 
• 83948-28-1 N-(trimethylsilyl)cinnamaldimine 

Downstream Products

• 96735-59-0 (S)-3-((R)-1-Hydroxy-ethyl)-4-((E)-styryl)-azetidin-2-one 
• 96735-61-4 (S)-1-(tert-Butyl-dimethyl-silanyl)-3-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-4-((E)-styryl)-azetidin-2-one 

Relevant articles and documents

Stereocontrolled total synthesis of the chiral building block (3S,4R)-3-[(R)-1-hydroxyethyl]-4-acetyloxy-azetidin-2-one: A useful synthon for the synthesis of (+)-thienamycin, carbapenems and penems

A total stereocontrolled synthesis of (1), an intermediate in the synthesis of (+)-thienamycin, carbapenems and penems, based on a strategy that uses the S(-)hydroxyethylbutyrate as chiral building block, is reported.