Cas 112100-10-4,(2S,5R,6R)-1-aza-3,3'-dimethyl-6-(4-N-benzyloxycarbonylbutanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester

112100-10-4

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Basic information

Product Name: (2S,5R,6R)-1-aza-3,3'-dimethyl-6-(4-N-benzyloxycarbonylbutanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester
Synonyms:
CAS NO:112100-10-4
Molecular Formula:
Molecular Weight: 555.609
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-(4-N-benzyloxycarbonylbutanamido)-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-(4-N-benzyloxycarbonylbutanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester(112100-10-4)
EPA Substance Registry System: (2S,5R,6R)-1-aza-3,3'-dimethyl-6-(4-N-benzyloxycarbonylbutanamido)-7-oxo-4-thiabicyclo<3.2.0>heptane-2-carboxylic acid p-nitrobenzyl ester(112100-10-4)

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: 112100-10-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112100-10-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,1,0 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 112100-10:
(8*1)+(7*1)+(6*2)+(5*1)+(4*0)+(3*0)+(2*1)+(1*0)=34
34 % 10 = 4
So 112100-10-4 is a valid CAS Registry Number.

112100-10-4Upstream product

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112100-10-4Relevant 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 (2007/10/02)

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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