247115-21-5

Basic information

• Product Name: (2S,3R,5R)-3-Acetoxymethyl-3-methyl-7-oxo-6-[1-pyridin-2-yl-meth-(Z)-ylidene]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester
• CAS NO: 247115-21-5
• Molecular Weight: 514.602
• Mol File: 247115-21-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: (2S,3R,5R)-3-Acetoxymethyl-3-methyl-7-oxo-6-[1-pyridin-2-yl-meth-(Z)-ylidene]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R,5R)-3-Acetoxymethyl-3-methyl-7-oxo-6-[1-pyridin-2-yl-meth-(Z)-ylidene]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester(247115-21-5)
• EPA Substance Registry System: (2S,3R,5R)-3-Acetoxymethyl-3-methyl-7-oxo-6-[1-pyridin-2-yl-meth-(Z)-ylidene]-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester(247115-21-5)

Safety Data

• Hazardous Substances Data: 247115-21-5(Hazardous Substances Data)

Upstream product

• 38700-15-1 triphenyl-(2-pyridylmethyl)phosphonium chloride 
• 247115-19-1 (2S,3R,5R)-3-Acetoxymethyl-3-methyl-6,7-dioxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 
• 47547-28-4 6-aminopenicillanic acid diphenylmethyl ester 
• 247114-99-4 (2S,3R,5R,6R)-3-Acetoxymethyl-6-allyloxycarbonylamino-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 
• 247115-14-6 (2S,3R,5R,6R)-3-Acetoxymethyl-6-amino-3-methyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 
• 211623-24-4 (2S,4S,5R,6R)-6-Allyloxycarbonylamino-3,3-dimethyl-4,7-dioxo-4λ⁴-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 
• 211623-25-5 (R)-benzhydryl 2-((2R,3R)-3-(allyloxycarbonyl)amino-2-(benzo[d]thiazol-2-yldisulfanyl)-4-oxoazetidin-1-yl)-3-methylbut-3-enoate 
• 121464-10-6 benzhydryl 6-(allyloxycarbonylamino)penicillinate 

Relevant articles and documents

The synthesis and evaluation of 6-alkylidene-2'β-substituted penam sulfones as β-lactamase inhibitors

Penicillin sulfones, which structurally incorporate both a 6-position alkylidene substituent and a 2'β substituent, have been synthesized and evaluated as inhibitors of class C and class A serine β-lactamases. Incorporation of the 2'β-substituent generall