161675-43-0

Basic information

• Product Name: [6R-[3(E),6α,7β]]-3-[(1-Cyclopropyl-2-oxo-3-pyrrolidinylidene)-methyl]-7-[[(1,1-dimethylethoxy)carbonyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester
• Synonyms: [6R-[3(E),6α,7β]]-3-[(1-Cyclopropyl-2-oxo-3-pyrrolidinylidene)-methyl]-7-[[(1,1-dimethylethoxy)carbonyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester
• CAS NO: 161675-43-0
• Molecular Weight: 601.723
• Mol File: 161675-43-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: [6R-[3(E),6α,7β]]-3-[(1-Cyclopropyl-2-oxo-3-pyrrolidinylidene)-methyl]-7-[[(1,1-dimethylethoxy)carbonyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [6R-[3(E),6α,7β]]-3-[(1-Cyclopropyl-2-oxo-3-pyrrolidinylidene)-methyl]-7-[[(1,1-dimethylethoxy)carbonyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester(161675-43-0)
• EPA Substance Registry System: [6R-[3(E),6α,7β]]-3-[(1-Cyclopropyl-2-oxo-3-pyrrolidinylidene)-methyl]-7-[[(1,1-dimethylethoxy)carbonyl]amino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid diphenylmethyl ester(161675-43-0)

Safety Data

• Hazardous Substances Data: 161675-43-0(Hazardous Substances Data)

Upstream product

• 135263-64-8 Diphenylmethyl [6R-(6α,7β)]-7-[[(1,1-dimethylethoxy)carbonyl]amino]-3-formyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate 
• 144-55-8 sodium hydrogencarbonate 
• 7487-88-9 magnesium sulfate 
• 865-47-4 potassium tert-butylate 
• 161754-80-9 (Z)-(2R,6R,7R)-7-tert-Butoxycarbonylamino-3-(1-cyclopropyl-2-oxo-pyrrolidin-3-ylidenemethyl)-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester 
• 148776-24-3 N-cyclopropyl-2,4-dibromobutyrylamide 
• 148776-25-4 N-cyclopropyl-3-bromopyrrolidin-2-one 

Relevant articles and documents

Process for producing cephalosporin derivatives

The present invention is concerned with a novel process for the manufacture of cephalosporin derivatives of the formula by converting a phosphonium salt into the corresponding ylide and reacting same with an aldehyde wherein R1 and R2 /su

Synthesis and structure-activity relationship of (lactamylvinyl)cephalosporins exhibiting activity against staphylococci, pneumococci, and enterococci

The synthesis and structure-activity relationships of a new class of vinylcephalosporins substituted with a lactamyl residue (1) are described. These compounds show excellent activity against enterococci and retain the broad spectrum activity of third-gen