101067-93-0

Basic information

• Product Name: Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester
• CAS NO: 101067-93-0
• Molecular Weight: 305.331
• Mol File: 101067-93-0.mol

Chemical Properties

• CAS DataBase Reference: Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester(101067-93-0)
• EPA Substance Registry System: Benzoic acid (R)-1-((2R,3S)-2-ethoxycarbonylmethyl-4-oxo-azetidin-3-yl)-ethyl ester(101067-93-0)

Safety Data

• Hazardous Substances Data: 101067-93-0(Hazardous Substances Data)

Upstream product

• 18295-66-4 1-ethoxy-1-(trimethylsiloxy)ethene 
• 101067-92-9 Benzoic acid (R)-1-((2S,3R)-2-acetoxy-4-oxo-azetidin-3-yl)-ethyl ester 
• 65-85-0 benzoic acid 
• 101067-91-8 Benzoic acid (R)-1-((2R,3S)-2-acetyl-4-oxo-azetidin-3-yl)-ethyl ester 
• 101067-90-7 Benzoic acid (R)-1-((3S,4R)-2-oxo-4-trimethylsilanylethynyl-azetidin-3-yl)-ethyl ester 

Relevant articles and documents

A FACILE, STEREOCONTROLLED ENTRY TO KEY INTERMEDIATES FOR THIENAMYCIN SYNTHESIS FROM ETHYL (S)-3-HYDROXYBUTANOATE

A new synthetic approach to optically active key intermediates for thienamycin synthesis is described which involves the highly stereocontrolled transformation of the 2-azetidinone obtained via the condensation of ethyl (S)-3-hydroxybutanoate with the N-s