92411-47-7

Basic information

• Product Name: [(2R,3S)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-(2-fluoro-ethylsulfanylthiocarbonylsulfanyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester
• Synonyms: [(2R,3S)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-(2-fluoro-ethylsulfanylthiocarbonylsulfanyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester
• CAS NO: 92411-47-7
• Molecular Weight: 590.79
• Mol File: 92411-47-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [(2R,3S)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-(2-fluoro-ethylsulfanylthiocarbonylsulfanyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [(2R,3S)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-(2-fluoro-ethylsulfanylthiocarbonylsulfanyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester(92411-47-7)
• EPA Substance Registry System: [(2R,3S)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-2-(2-fluoro-ethylsulfanylthiocarbonylsulfanyl)-4-oxo-azetidin-1-yl]-oxo-acetic acid 4-nitro-benzyl ester(92411-47-7)

Safety Data

• Hazardous Substances Data: 92411-47-7(Hazardous Substances Data)

Upstream product

• 76899-07-5 (3R,4R)-3-[(R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-acetoxyazetidin-2-one 
• 81779-73-9 chloroxoacetic acid (4-nitrophenyl)methyl ester 
• 85905-08-4 (3S,4R)-3-<(1R)-1-tert-butyldimethylsilyloxyethyl>-4-<<(2-fluoroethylthio)thiocarbonyl>thio>azetidin-2-one 

Downstream Products

• 85905-02-8 (5S,6S)-6-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-3-(2-fluoro-ethylsulfanyl)-7-oxo-4-thia-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester 
• 111969-80-3 C₂₉H₄₆FN₂O₉PS₃Si 

Relevant articles and documents

EFFICIENT SYNTHESES OF A NEW PENEM ANTIBIOTIC, SODIUM (5R,6S)-2-(2-FLUOROETHYLTHIO)-6-PENEM-3-CARBOXYLATE

Two useful routes to sodium (5R,6S)-2-(2-fluoroethylthio)-6-penem-3-carboxylate (1) via trithiocarbonate (3) are reported.An intramolecular Wittig reaction of 6 and an oxalimide cyclization of 9 with phosphite are employed as key steps.