3115-55-7

Basic information

• Product Name: 6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYL
• Synonyms: LABOTEST-BB LT00039160;6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYL
• CAS NO: 3115-55-7
• Molecular Formula: C₈H₁₂N₂O₃S
• Molecular Weight: 216.26
• Mol File: 3115-55-7.mol
• Article Data: 10

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYL(CAS DataBase Reference)
• NIST Chemistry Reference: 6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYL(3115-55-7)
• EPA Substance Registry System: 6-AMINO-3,3-DIMETHYL-7-OXO-4-THIA-1-AZA-BICYCLO[3.2.0]HEPTANE-2-CARBOXYL(3115-55-7)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 3115-55-7(Hazardous Substances Data)

Upstream product

• 496809-25-7 benzylpenicillin 
• 61-33-6 penicillin G 
• 40273-68-5 rac-6β-tritylamino-penicillanic acid benzyl ester 
• 97656-36-5 (4S)-2t-((R)-carboxy-tritylamino-methyl)-5,5-dimethyl-thiazolidine-4r-carboxylic acid benzyl ester 
• 113-98-4 Penicillin G potassium 
• 62-55-5 thioacetamide 
• 594-42-3 chlorothio-trichloro-methane 
• 75-78-5 dimethylsilicon dichloride 
• 40124-92-3 rac-6β-tritylamino-penicillanic acid 

Downstream Products

• 24158-88-1 6,6-dibromopenicillanic acid 
• 85573-73-5 2β-chloromethyl-2α-methylpenicillin-3α-carboxylic acid diphenylmethyl ester 
• 89051-48-9 Benzhydryl 2β-bromomethyl-2α-methyl-6,6-dihydropenicillanate 
• 205320-23-6 benzhydryl-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylate-4-oxide 
• 80353-26-0 Benzhydryl 6α-bromopenicillanate-1-oxide 
• 85573-72-4 (R)-2-[2-(benzothiazol-2-yldisulfanyl)-4-oxo-azetidin-1-yl]-3-methyl-butyl-3-enoic acid benzhydryl ester 
• 32886-98-9 Cyanomethyl 6-aminopenicillanate p-toluenesulfonate 
• 61-33-6 penicillin G 
• 37880-24-3 N-Salicylidene-6-aminopenicillanic Acid Sulfoxide 

Relevant articles and documents

Enzymatic hydrolysis of β-lactam antibiotics at low pH in a two-phase "aqueous solution - Water-immiscible organic solvent" system

The application of the two-phase "aqueous solution - water-immiscible organic solvent" system is suggested not for effective biocatalytic synthesis, but for hydrolytic purposes. Enzymatic hydrolysis of benzylpenicillin and N-phenylacetamidodesacetoxycepha

Extractive deacylation of benzylpenicillin in aqueous two-phase systems

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Process for producing 6-aminopenicillanic acid or 7-aminocephalosporanic acid derivatives

A derivative of 6-aminopenicillanic acid or 7-aminocephalosporanic acid is produced by a process which comprises disulfidizing a 6-thioacylaminopenicillanic acid or 7-thioacylaminocephalosporanic acid compound to obtain a corresponding disulfide compound, and then solvolyzing the disulfide compound. The process is novel and industrially feasible for producing the amino compound, which is not accompanied by "reconversion reaction".