Cas 112078-58-7,(2S,5R,6R)-1-aza-3,3'-dimethyl-6-(5-p-nitrobenzyloxycarbonylpentanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester

112078-58-7

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Basic information

Product Name: (2S,5R,6R)-1-aza-3,3'-dimethyl-6-(5-p-nitrobenzyloxycarbonylpentanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester
Synonyms:
CAS NO:112078-58-7
Molecular Formula:
Molecular Weight: 614.633
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)-1-aza-3,3'-dimethyl-6-(5-p-nitrobenzyloxycarbonylpentanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2S,5R,6R)-1-aza-3,3'-dimethyl-6-(5-p-nitrobenzyloxycarbonylpentanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester(112078-58-7)
EPA Substance Registry System: (2S,5R,6R)-1-aza-3,3'-dimethyl-6-(5-p-nitrobenzyloxycarbonylpentanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester(112078-58-7)

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: 112078-58-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112078-58-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,7 and 8 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 112078-58:
(8*1)+(7*1)+(6*2)+(5*0)+(4*7)+(3*8)+(2*5)+(1*8)=97
97 % 10 = 7
So 112078-58-7 is a valid CAS Registry Number.

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112078-58-7Relevant academic research and scientific papers

THE ENZYMATIC RING EXPANSION OF PENICILLINS TO CEPHALOSPORINS: SIDE CHAIN SPECIFICITY

Baldwin, Jack E.,Adlington, Robert M.,Crabbe, M. James,Knight, Graham,Nomoto, Takashi,et al.

, p. 3009 - 3014 (1987)

Structural variants of the acylamino side chain of penicillins have been tested as substrates for Deacetoxy/Deacetyl Cephalosporin C Synthetase from C. acremonium CO 728.A six carbon chain terminating in a carboxyl group was found to permit efficient ring expansion to cephems, with the exception of δ-(L-α-aminoadipoyl).

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