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(6R,7R)-3-Chloromethyl-4-methyl-8-oxo-7-(2-thiophen-2-yl-acetylamino)-5-thia-1-aza-bicyclo[4.2.0]oct-3-ene-2-carboxylic acid benzhydryl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

87263-06-7

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87263-06-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87263-06-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,6 and 3 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 87263-06:
(7*8)+(6*7)+(5*2)+(4*6)+(3*3)+(2*0)+(1*6)=147
147 % 10 = 7
So 87263-06-7 is a valid CAS Registry Number.

87263-06-7Relevant academic research and scientific papers

2 - Substituted cephem compound-containing pharmaceutical composition

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Paragraph 0243; 0244, (2018/10/03)

PROBLEM TO BE SOLVED: To provide a cephem compound which has a strong antimicrobial activity, in particular effective against various β-lactamase producing Gram negative bacteria, and a composition comprising the compound.SOLUTION: The present invention provides a pharmaceutical composition comprising a compound represented by formula (I), an ester at a carboxyl group, an amino-protected compound when the amino is present on a ring in the 7-side chain, or a pharmaceutically acceptable salt thereof.

2 SUBSTITUTED CEPHEM COMPOUNDS

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Paragraph 0182, (2014/05/24)

The compounds of formula (I) of the subject invention are related to 2-substituted cephem compounds, which have a wide antimicrobial spectrum, in particular exhibit potent antimicrobial activity against beta-lactamase producing Gram negative bacteria, and pharmaceutical compositions comprising the same.

Synthesis of 2α-methyl- and 2β-methyl-3-(substituted methyl)cephalosporins, and 2,3-diexomethylenecepham

Mizokami,Fukase,Horii,Kuwada

, p. 1482 - 1493 (2007/10/02)

The stereoselective synthesis of 2α-methyl- and 2β-methyl-3-(substituted methyl)- cephalosporins via 2-methyl-3-formyloxymethylceph-2-em (5) and 2-methyl-3-acetoxymethylceph-2-em (16) from 2-methylene-3-acetoxymethylcephalosporin (1) is described. Reducti

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