37591-56-3

Basic information

• Product Name: benzhydryl 6β-(phenylacetamido)penicillanate 1β-oxide
• Synonyms: benzhydryl 6β-(phenylacetamido)penicillanate 1β-oxide
• CAS NO: 37591-56-3
• Molecular Weight: 516.618
• Mol File: 37591-56-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: benzhydryl 6β-(phenylacetamido)penicillanate 1β-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: benzhydryl 6β-(phenylacetamido)penicillanate 1β-oxide(37591-56-3)
• EPA Substance Registry System: benzhydryl 6β-(phenylacetamido)penicillanate 1β-oxide(37591-56-3)

Safety Data

• Hazardous Substances Data: 37591-56-3(Hazardous Substances Data)

Upstream product

• 67565-52-0 diphenylmethyl 6β-(2-phenylacetamido)penicillanate 
• 101760-73-0 (2S,5R,6R)-6-(Bis-phenylacetyl-amino)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 
• 114-70-5 sodium phenylacetate 
• 101760-76-3 (2S,4R,5R,6R)-6-(Bis-phenylacetyl-amino)-3,3-dimethyl-4,7-dioxo-4λ⁴-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 
• 66363-41-5 (S)-3,3-Dimethyl-7-oxo-6-phenylacetylamino-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzhydryl ester 

Downstream Products

• 51415-50-0 10-chloro-6β-(2-phenyl-acetylamino)-penicillanic acid benzhydryl ester 
• 100349-41-5 (2S,4S,5R,6S)-6-bromo-3,3-dimethyl-4,7-dioxo-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylic acid benzhydryl ester 
• 100349-42-6 (2S,4S,5R)-3,3-dimethyl-4,7-dioxo-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylic acid benzhydryl ester 
• 78037-13-5 (R)-2-((1S,5R)-3-Benzyl-7-oxo-4-oxa-2,6-diaza-bicyclo[3.2.0]hept-2-en-6-yl)-3-methyl-but-3-enoic acid benzhydryl ester 
• 100298-43-9 benzhydryl 6-diazopenicillanate 1β-oxide 

Relevant articles and documents

A practical method for synthesis of penicillin and cephalosporin sulfoxides

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Process for the preparation of esters of N-blocked penicillin acids which comprises reacting the acid or a salt thereof with a primary amine and a nitrosating agent

A process is described for the preparation of esters of N-blocked amino acids (such as penicillins or cephalosporins) wherein the amino acid or a salt thereof is reacted with a primary amine and nitrosating agent.