182268-32-2

Basic information

• Product Name: benzyl (2S)-2-[(3R,4S)-4-chloro-3-phthalimido-2-oxazetidin-1-yl]-2-(1-chlorothio-1-methylethyl)-acetate
• CAS NO: 182268-32-2
• Molecular Weight: 507.394
• Mol File: 182268-32-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: benzyl (2S)-2-[(3R,4S)-4-chloro-3-phthalimido-2-oxazetidin-1-yl]-2-(1-chlorothio-1-methylethyl)-acetate(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl (2S)-2-[(3R,4S)-4-chloro-3-phthalimido-2-oxazetidin-1-yl]-2-(1-chlorothio-1-methylethyl)-acetate(182268-32-2)
• EPA Substance Registry System: benzyl (2S)-2-[(3R,4S)-4-chloro-3-phthalimido-2-oxazetidin-1-yl]-2-(1-chlorothio-1-methylethyl)-acetate(182268-32-2)

Safety Data

• Hazardous Substances Data: 182268-32-2(Hazardous Substances Data)

Upstream product

• 551-16-6 6-Aminopenicillanic Acid 
• 22509-74-6 N-ethoxycarbonylphthalimide 
• 20425-27-8 (2S,5R,6R)-6-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid 
• 59034-26-3 (2S,5R,6R)-benzyl 6-(1,3-dioxoisoindolin-2-yl)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 

Downstream Products

• 182268-25-3 benzyl (2S)-2-[(3S,4R)-4-chloro-3-phthalimido-2-oxazetidin-1-yl]-2-(1-chlorothio-1-methylethyl)-acetate 
• 182268-26-4 (2S,5S,6S)-benzyl 6-(1,3-dioxoisoindolin-2-yl)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 
• 182268-27-5 benzyl (-)-(2S,4S,5S,6S)-3,3-dimethyl-7-oxo-6-phthalimido-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate-4-oxide 
• 182268-33-3 benzyl (-)-(2S,4S,5S,6R)-3,3-dimethyl-7-oxo-6-phthalimido-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate 4-oxide 
• 182268-37-7 benzyl (-)-(6S,7S)-3-methyl-7-(4-nitrobenzenesulfenamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182186-39-6 benzyl (-)-(6S,7R)-3-methyl-7-(4-nitrobenzenesulfenamido)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182268-29-7 benzyl (-)-(6S,7S)-3-methyl-8-oxo-7-phenoxyacetamido-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182268-38-8 benzyl (-)-(6S,7R)-3-methyl-8-oxo-7-phenoxyacetamido-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182268-35-5 benzyl (-)-(6S,7S)-3-methyl-7-(4-nitrobenzylideneamino)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182186-35-2 (6S,7S)-benzyl 7-(1,3-dioxoisoindolin-2-yl)-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182186-38-5 benzyl (-)-(6S,7R)-3-methyl-8-oxo-7-phthalimido-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182186-48-7 benzyl (-)-(6S,7S)-3-methyl-8-oxo-5-thia-7-(4-toluenesulfenamido)-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182268-28-6 benzyl (-)-(6S,7S)-7-amino-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 182268-34-4 benzyl (-)-(6S,7R)-7-amino-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 

Relevant articles and documents

Asymmetric synthesis of new β-lactam lipopeptides as bacterial signal peptidase i inhibitors

The transmembrane bacterial enzyme, signal peptidase I, is recognized as being a promising target for reducing the emergence of drug resistance. The asymmetric synthesis and the biological evaluation of original β-lactam lipopeptides have been performed t