Cas 115391-30-5,(2S,5R,6S)-3,3-Dimethyl-4,4,7-trioxo-6-(2-phenoxy-acetylamino)-4λ<sup>6</sup>-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester

115391-30-5

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Basic information

Product Name: (2S,5R,6S)-3,3-Dimethyl-4,4,7-trioxo-6-(2-phenoxy-acetylamino)-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester
Synonyms:
CAS NO:115391-30-5
Molecular Formula:
Molecular Weight: 517.516
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,6S)-3,3-Dimethyl-4,4,7-trioxo-6-(2-phenoxy-acetylamino)-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5R,6S)-3,3-Dimethyl-4,4,7-trioxo-6-(2-phenoxy-acetylamino)-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester(115391-30-5)
EPA Substance Registry System: (2S,5R,6S)-3,3-Dimethyl-4,4,7-trioxo-6-(2-phenoxy-acetylamino)-4λ⁶-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 4-nitro-benzyl ester(115391-30-5)

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: 115391-30-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 115391-30-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,3,9 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 115391-30:
(8*1)+(7*1)+(6*5)+(5*3)+(4*9)+(3*1)+(2*3)+(1*0)=105
105 % 10 = 5
So 115391-30-5 is a valid CAS Registry Number.

115391-30-5Upstream product

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115391-30-5Relevant academic research and scientific papers

RETENTION OF STEREOCHEMISTRY IN THE RING-OPENING OF PENICILLIN V SULPHONE p-NITROBENZYL ESTER

Davis, Michael,Wu, Wen-Yang

, p. 183 - 188 (2007/10/02)

By careful control of the basic catalyst, the solvent, and the temperature, p-nitrobenzyl phenoxymethylpenicillinate 1,1-dioxide (penicillin V sulphone p-nitrobenzyl ester) (1d) can be converted into (2R,3R)-1-2-methyl-(p-nitrobenzyloxycarbonyl)prop-1-en

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