162515-03-9

Basic information

• Product Name: (2S,3S,5R)-3-((E)-2-Chloro-vinyl)-3-methyl-4,4,7-trioxo-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester
• Synonyms: (2S,3S,5R)-3-((E)-2-Chloro-vinyl)-3-methyl-4,4,7-trioxo-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester
• CAS NO: 162515-03-9
• Molecular Weight: 445.923
• Mol File: 162515-03-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3S,5R)-3-((E)-2-Chloro-vinyl)-3-methyl-4,4,7-trioxo-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3S,5R)-3-((E)-2-Chloro-vinyl)-3-methyl-4,4,7-trioxo-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester(162515-03-9)
• EPA Substance Registry System: (2S,3S,5R)-3-((E)-2-Chloro-vinyl)-3-methyl-4,4,7-trioxo-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester(162515-03-9)

Safety Data

• Hazardous Substances Data: 162515-03-9(Hazardous Substances Data)

Upstream product

• 5350-57-2 benzophenone hydrazone 
• 87579-79-1 (R)-benzhydryl 2-((R)-2-(benzo[d]thiazol-2-yldisulfanyl)-4-oxoazetidin-1-yl)-3-methylbut-3-enoate 
• 162514-95-6 diphenylmethyl (2S,3R,5R)-3-formyl-3-methyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 
• 162514-96-7 benzhydryl (2S,3R,5R)-3-hydroxymethyl-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate 
• 100349-41-5 (2S,4S,5R,6S)-6-bromo-3,3-dimethyl-4,7-dioxo-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylic acid benzhydryl ester 
• 100349-42-6 (2S,4S,5R)-3,3-dimethyl-4,7-dioxo-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylic acid benzhydryl ester 
• 551-16-6 6-Aminopenicillanic Acid 
• 162515-01-7 Benzhydryl (E,Z)-(2S,3S,5R)-3-(2-chloro-vinyl)-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylate 

Relevant articles and documents

Design, synthesis, and evaluation of 2β-alkenyl penam sulfone acids as inhibitors of β-lactamases

A general method for synthesis of 2β-alkenyl penam sulfones has been developed. The new compounds inhibited most of the common types of β- lactamase. The level of activity depended very strongly on the nature of the substituent in the 2β-alkenyl group. Th