Cas 88587-31-9,(4S,5S,6S)-4-Methyl-6-[(R)-1-(4-nitro-benzyloxycarbonyloxy)-ethyl]-7-oxo-3-(pyrimidin-2-ylsulfanyl)-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester

88587-31-9

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Basic information

Product Name: (4S,5S,6S)-4-Methyl-6-[(R)-1-(4-nitro-benzyloxycarbonyloxy)-ethyl]-7-oxo-3-(pyrimidin-2-ylsulfanyl)-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester
Synonyms:
CAS NO:88587-31-9
Molecular Formula:
Molecular Weight: 635.611
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: (4S,5S,6S)-4-Methyl-6-[(R)-1-(4-nitro-benzyloxycarbonyloxy)-ethyl]-7-oxo-3-(pyrimidin-2-ylsulfanyl)-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (4S,5S,6S)-4-Methyl-6-[(R)-1-(4-nitro-benzyloxycarbonyloxy)-ethyl]-7-oxo-3-(pyrimidin-2-ylsulfanyl)-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester(88587-31-9)
EPA Substance Registry System: (4S,5S,6S)-4-Methyl-6-[(R)-1-(4-nitro-benzyloxycarbonyloxy)-ethyl]-7-oxo-3-(pyrimidin-2-ylsulfanyl)-1-aza-bicyclo[3.2.0]hept-2-ene-2-carboxylic acid 4-nitro-benzyl ester(88587-31-9)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 88587-31-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88587-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,8 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 88587-31:
(7*8)+(6*8)+(5*5)+(4*8)+(3*7)+(2*3)+(1*1)=189
189 % 10 = 9
So 88587-31-9 is a valid CAS Registry Number.

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88587-31-9Relevant academic research and scientific papers

A STEREOCONTROLLED ROUTE TO OPTICALLY ACTIVE 1-METHYL CARBAPENEMS

Brown, Pamela,Southgate, Robert

, p. 247 - 250 (1986)

Using a stereoselective carbene insertion reaction to form the β-lactam ring, optically active 1-methyl carbapenems have been prepared.

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