Cas 192764-48-0,benzoic Acid (6R,7S)-2-tert-butylsulfanylcarbonyl-7-methoxy-3-methyl-5,5,8-trioxo-5-thia-1-aza-bicyclo [4.2.0]oct-2-en-4-yl Ester

192764-48-0

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Basic information

Product Name: benzoic Acid (6R,7S)-2-tert-butylsulfanylcarbonyl-7-methoxy-3-methyl-5,5,8-trioxo-5-thia-1-aza-bicyclo [4.2.0]oct-2-en-4-yl Ester
Synonyms: benzoic Acid (6R,7S)-2-tert-butylsulfanylcarbonyl-7-methoxy-3-methyl-5,5,8-trioxo-5-thia-1-aza-bicyclo [4.2.0]oct-2-en-4-yl Ester
CAS NO:192764-48-0
Molecular Formula:
Molecular Weight: 453.537
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: benzoic Acid (6R,7S)-2-tert-butylsulfanylcarbonyl-7-methoxy-3-methyl-5,5,8-trioxo-5-thia-1-aza-bicyclo [4.2.0]oct-2-en-4-yl Ester(CAS DataBase Reference)
NIST Chemistry Reference: benzoic Acid (6R,7S)-2-tert-butylsulfanylcarbonyl-7-methoxy-3-methyl-5,5,8-trioxo-5-thia-1-aza-bicyclo [4.2.0]oct-2-en-4-yl Ester(192764-48-0)
EPA Substance Registry System: benzoic Acid (6R,7S)-2-tert-butylsulfanylcarbonyl-7-methoxy-3-methyl-5,5,8-trioxo-5-thia-1-aza-bicyclo [4.2.0]oct-2-en-4-yl Ester(192764-48-0)

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: 192764-48-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 192764-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,7,6 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 192764-48:
(8*1)+(7*9)+(6*2)+(5*7)+(4*6)+(3*4)+(2*4)+(1*8)=170
170 % 10 = 0
So 192764-48-0 is a valid CAS Registry Number.

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192764-48-0Relevant academic research and scientific papers

4-SUBSTITUTED CEPHEM DERIVATIVES AS ELASTASE INHIBITORS

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, (2008/06/13)

The present invention relates to cephem-derivatives and to a process for their preparation, having proper substituents at C-2 position, i.e. heterocyclylthio or acyloxy group. They are potent protease inhibitors, in particular human leucocyte elastase (HL

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