96035-08-4

Basic information

• Product Name: (2S,4R)-2-carbamoyl-4-mesyloxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine
• Synonyms: (2S,4R)-2-carbamoyl-4-mesyloxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine
• CAS NO: 96035-08-4
• Molecular Weight: 387.37
• Mol File: 96035-08-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,4R)-2-carbamoyl-4-mesyloxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,4R)-2-carbamoyl-4-mesyloxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine(96035-08-4)
• EPA Substance Registry System: (2S,4R)-2-carbamoyl-4-mesyloxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine(96035-08-4)

Safety Data

• Hazardous Substances Data: 96035-08-4(Hazardous Substances Data)

Upstream product

• 4457-32-3 4-nitrobenzyl chloroformate 
• 51-35-4 4R-4-hydroxyproline 
• 101803-29-6 (2S,4R)-4-hydroxy-2-methoxycarbonyl-1-(4-nitrobenzyloxycarbonyl)pyrrolidine 
• 96034-57-0 (2S,4R)-4-Hydroxy-1-(4-nitrobenzyloxycarbonyl)pyrrolidine-2-carboxylic acid 
• 138324-82-0 (2S,4R)-4-mesyloxy-1-(p-nitrobenzyloxycarbonyl)pyrrolidine-2-carboxylic acid methyl ester 

Downstream Products

• 117336-17-1 (2S,4R)-4-methanesulfonyloxy-1-(4-nitrobenzyloxycarbonyl)-2-thiocarbamoylpyrrolidine 
• 230964-57-5 p-nitrobenzyl (1R,5S,6S)-6-<(1R)-1-hydroxyethyl>-2-<(5S,7S)-2,2,3-trimethyl-4-oxo-1,3-diazabicyclo<3.3.0>octan-7-ylthio>-1-methylcarbapen-2-em-3-carboxylate 
• 474670-86-5 (4R,5S,6S)-6-((R)-1-Hydroxy-ethyl)-4-methyl-3-((6S,7aS)-3-methyl-1-oxo-3-phenyl-hexahydro-pyrrolo[1,2-c]imidazol-6-ylsulfanyl)-7-oxo-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 
• 474670-58-1 thioacetic acid S-(3-methyl-1-oxo-3-phenyl-hexahydro-pyrrolo[1,2-c]imidazol-6-yl) ester 

Relevant articles and documents

Synthesis and antibacterial activity of 1β-methylcarbapenem having a 1,3-diazabicyclo[3.3.0]octan-4-one moiety, Part II

The synthesis of a new series of 1β-methylcarbapenems having a 1,3- diazabicyclo[3.3.0]octan-4-one moiety is described. Their in vitro antibacterial activities against both Gram-positive and Gram-negative bacteria are tested and the effect of substituent on the bicyclic ring was investigated. A particular compound (11h) having aminoethyl group showed the most potent antibacterial activity.