75007-69-1

Upstream product

• 86862-92-2 diphenylmethyl <4-<(benzyloxycarbonyl)oxy>phenyl>acetate 
• 86862-84-2 Carbonic acid benzyl ester 4-chlorocarbonylmethyl-phenyl ester 
• 86862-83-1 <4-<(benzyloxycarbonyl)oxy>phenyl>acetic acid 
• 78984-21-1 diphenylmethyl (4-hydroxyphenyl)acetate 
• 66429-65-0 (6R)-7t-amino-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-(6rH)-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester 
• 156-38-7 4-hydroxyphenylacetate 
• 86862-86-4 (6R,7S)-7-[2-(4-Benzyloxycarbonyloxy-phenyl)-acetylamino]-3-(1-methyl-1H-tetrazol-5-ylsulfanylmethyl)-8-oxo-5-oxa-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid benzhydryl ester 

Relevant academic research and scientific papers

Synthesis and Substituent Effects on Antibacterial Activity, Alkaline Hydrolysis Rates, and Infrared Absorption Frequencies of Some Cephem Analogues Related to Latamoxef (Moxalactam)

Relationships between intrinsic antibacterial activity and β-lactam reactivity of 7β-amino- and 7β-amino derivatives of 1-oxa- and 1-thiacephems, with or without the 7α-methoxy group (1-8), were investiga