Cas 95361-55-0,(2S,5R,6R)-6-(Benzothiazol-2-ylsulfanylamino)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester

95361-55-0

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Basic information

Product Name: (2S,5R,6R)-6-(Benzothiazol-2-ylsulfanylamino)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester
Synonyms: (2S,5R,6R)-6-(Benzothiazol-2-ylsulfanylamino)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester
CAS NO:95361-55-0
Molecular Formula:
Molecular Weight: 471.625
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (2S,5R,6R)-6-(Benzothiazol-2-ylsulfanylamino)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5R,6R)-6-(Benzothiazol-2-ylsulfanylamino)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester(95361-55-0)
EPA Substance Registry System: (2S,5R,6R)-6-(Benzothiazol-2-ylsulfanylamino)-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid benzyl ester(95361-55-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 95361-55-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 95361-55-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,3,6 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 95361-55:
(7*9)+(6*5)+(5*3)+(4*6)+(3*1)+(2*5)+(1*5)=150
150 % 10 = 0
So 95361-55-0 is a valid CAS Registry Number.

95361-55-0Upstream product

95361-55-0Downstream Products

95361-53-8 C₂₂H₁₉N₃O₃S₃

95361-55-0Relevant academic research and scientific papers

MgBr2-PROMOTED ELECTROSYNTHESIS OF SULFENIMINES (THIOOXIMES) FROM α-AMINO-ALKANOATES AND DIARYL/DIALKYL DISULFIDES IN A CH2Cl2-H2O TWO-PHASE SYSTEM. A STRAIGHTFORWARD PREPARATION OF C(6)/C(7)-SULFENIMINE DERIVATIVES OF PENICILLIN AND CEPHALOSPORIN

Torii, Sigeru,Tanaka, Hideo,Hamano, Sin-ichi,Tada, Nobuhito,Nokami, Junzo,Sasaoka, Michio

, p. 1823 - 1826 (2007/10/02)

Direct transformation of α-aminoalkanoates and diaryl or dialkyl disulfides to the corresponding sulfenimines by electrolysis in a CH2Cl2-H2O-MgBr2-(Pt electrodes) system and its application to the sulfenylation of C(6)/C(7)-amino groups of penicillin and cephalosporin are described.

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