185675-66-5

Basic information

• Product Name: (1S,5S,8aS,8bR)-5-(Benzyloxycarbonyl-methyl-amino)-1-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-1,2,5,6,7,8,8a,8b-octahydro-azeto[2,1-a]isoindole-4-carboxylic acid benzyl ester
• CAS NO: 185675-66-5
• Molecular Weight: 618.846
• Mol File: 185675-66-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (1S,5S,8aS,8bR)-5-(Benzyloxycarbonyl-methyl-amino)-1-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-1,2,5,6,7,8,8a,8b-octahydro-azeto[2,1-a]isoindole-4-carboxylic acid benzyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,5S,8aS,8bR)-5-(Benzyloxycarbonyl-methyl-amino)-1-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-1,2,5,6,7,8,8a,8b-octahydro-azeto[2,1-a]isoindole-4-carboxylic acid benzyl ester(185675-66-5)
• EPA Substance Registry System: (1S,5S,8aS,8bR)-5-(Benzyloxycarbonyl-methyl-amino)-1-[(R)-1-(tert-butyl-dimethyl-silanyloxy)-ethyl]-2-oxo-1,2,5,6,7,8,8a,8b-octahydro-azeto[2,1-a]isoindole-4-carboxylic acid benzyl ester(185675-66-5)

Safety Data

• Hazardous Substances Data: 185675-66-5(Hazardous Substances Data)

Upstream product

• 181228-87-5 (3S,4R)-3-[(1R)-1-(tert-butyldimethylsilyloxy)ethyl]-4-[(1S,2S,6R)-1-hydroxy-2-methylaminocyclohexyl-6-yl]azetidin-2-one 
• 185675-65-4 ((1S,3R)-3-{(2R,3S)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-oxo-cyclohexyl)-methyl-carbamic acid benzyl ester 
• 300568-72-3 ((1S,2S,3R)-3-{(2R,3S)-3-[(R)-1-(tert-Butyl-dimethyl-silanyloxy)-ethyl]-4-oxo-azetidin-2-yl}-2-hydroxy-cyclohexyl)-methyl-carbamic acid benzyl ester 
• 501-53-1 benzyl chloroformate 
• 35249-73-1 benzyl chlorooxalate 

Downstream Products

• 185675-67-6 (1S,5S,8aS,8bR)-5-(Benzyloxycarbonyl-methyl-amino)-1-((R)-1-hydroxy-ethyl)-2-oxo-1,2,5,6,7,8,8a,8b-octahydro-azeto[2,1-a]isoindole-4-carboxylic acid benzyl ester 

Relevant articles and documents

Synthesis and antibacterial activity of 4-ureido trinems

This article describes studies carried out on the synthesis and biological activity of 4-ureido trinems 1 obtained by the condensation of various isocyanates and the intermediate 6. Among others, 4-N-methyl-N'-alkyl ureido trinems showed a promising antimicrobial activity against Gram-negative bacteria.