34582-70-2

Basic information

• Product Name: chloromethyl <2S-(2α,5α,6β)>-3,3-dimethyl-7-oxo-6-(2,6-dimethoxybenzamido)-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate
• Synonyms: chloromethyl <2S-(2α,5α,6β)>-3,3-dimethyl-7-oxo-6-(2,6-dimethoxybenzamido)-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate
• CAS NO: 34582-70-2
• Molecular Weight: 428.894
• Mol File: 34582-70-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: chloromethyl <2S-(2α,5α,6β)>-3,3-dimethyl-7-oxo-6-(2,6-dimethoxybenzamido)-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: chloromethyl <2S-(2α,5α,6β)>-3,3-dimethyl-7-oxo-6-(2,6-dimethoxybenzamido)-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate(34582-70-2)
• EPA Substance Registry System: chloromethyl <2S-(2α,5α,6β)>-3,3-dimethyl-7-oxo-6-(2,6-dimethoxybenzamido)-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate(34582-70-2)

Safety Data

• Hazardous Substances Data: 34582-70-2(Hazardous Substances Data)

Upstream product

• 49715-04-0 chlorosulfuric acid chloromethyl ester 
• 132-92-3 methicillin sodium 

Downstream Products

• 122648-68-4 <<(1,4-dihydro-1-methyl-3-pyridinyl)carbonyl>oxy>methyl <2S-(2α,5α,6β)>-3,3-dimethyl-7-oxo-6-(2,6-dimethoxybenzamido)-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate 
• 122648-61-7 <(3-pyridinylcarbonyl)oxy>methyl <2S-(2α,5α,6β)>-3,3-dimethyl-7-oxo-6-(2,6-dimethoxybenzamido)-4-thia-1-azabicyclo<3.2.0>heptane-2-carboxylate 

Relevant articles and documents

Chemical delivery systems for some penicillinase-resistant semisynthetic penicillins

Chemical delivery systems (CDS's) based on a dihydropyridine ? quaternary pyridinium ion redox system analogous to the naturally occurring NADH ? NAD+ system were synthesized for a group of staphylococcal penicillinase resistant penicillins, in

Pharmaceutical formulations for parenteral use

Aqueous parenteral solutions of drugs which are insoluble or only sparingly soluble in water and/or which are unstable in water, combined with cyclodextrin selected from the group consisting of hydroxypropyl, hydroxyethyl, glucosyl, maltosyl and maltotriosyl derivatives of β- and γ-cyclodextrin, provide a means for alleviating problems associated with drug precipitation at the injection site and/or in the lungs or other organs following parenteral administration.