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1H-1,2,4-Triazole-3-carboxamide,4,5-dihydro-4-methyl-5-thioxo-(9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61320-82-9

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61320-82-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61320-82-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,3,2 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 61320-82:
(7*6)+(6*1)+(5*3)+(4*2)+(3*0)+(2*8)+(1*2)=89
89 % 10 = 9
So 61320-82-9 is a valid CAS Registry Number.

61320-82-9Upstream product

61320-82-9Downstream Products

61320-82-9Relevant academic research and scientific papers

7-[2-(2-Imino-4-thiazolin-4-yl)-2-(syn)-hydroxy-iminoacetamido]-cephalosporins

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, (2008/06/13)

Disclosed are 2-(syn)-hydroxyimino-acetamide derivatives of the formula: STR1 wherein Y is hydrogen, hydroxyl, an acyloxy, carbamoyloxy, a quaternary ammonium or a nitrogen-containing heterocyclic ring-substituted thio group; or pharmaceutically acceptable salts or esters thereof are useful as antibacterial agents. Also disclosed are processes for producing them.

Cephalosporin displacement reaction

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, (2008/06/13)

The present invention is directed to a process for the displacement of the acetoxy group of a cephalosporanic acid by a sulfur nucleophile, in an organic solvent and under essentially anhydrous conditions.

Cephalosporin derivatives

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, (2008/06/13)

A series of novel 7-(Dα-aminophenylacetamido)- and 7-(D-α-hydroxyphenylacetamido)- Δ3 -cephem derivatives have been prepared wherein a heterocyclic thiomethyl moiety is located at the 3-position of the molecule. These compounds are useful as antibacterial agents for the treatment of diseases caused by Gram-positive and Gram-negative bacteria. Preferred members include 7-(D-α-hydroxyphenylacetamido)-3-(3-carbamoyl-1,2,4-triazol-5-yl)thiomethylceph-3-em-4-carboxylic acid and 7-(D-α-hydroxyphenylacetamido)-3-(2-carboxymethoxy-methyl-1,3,4-thiadiazol-5-yl)thiomethylceph-3-em-4-carboxylic acid. Alternative methods of preparation are provided for these compounds, including various synthetic routes leading to the required novel heterocyclic thiol intermediates.

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