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96133-99-2

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96133-99-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 96133-99-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,1,3 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 96133-99:
(7*9)+(6*6)+(5*1)+(4*3)+(3*3)+(2*9)+(1*9)=152
152 % 10 = 2
So 96133-99-2 is a valid CAS Registry Number.

96133-99-2Relevant academic research and scientific papers

Sulfamic acid-mediated, efficient, one-pot synthesis of novel 5-substituted 1,3,4-thiadiazol-2-ylcarbamoyl aliphatic amide acid derivatives and facile synthesis of cyclic amides

Toche,Janrao,Gangurde,Nikam

supporting information, p. 2527 - 2535 (2013/07/25)

Convenient and efficient one-pot syntheses of 5-substituted-1,3,4- thiadiazol-2- ylcarbamoyl aliphatic amide acid derivatives were described and developed using sulfamic acid catalyst. Thiosemicarbazide and substituted triethylorthoester and cyclic/alicyc

Derives de la dihydro-2,4 triazole-1,2,4 thione-3 et de l'amino-2 thiadiazole-1,3,4 a partir de nouvelles thiosemicarbazones d'esters

Malbec, Frederique,Milcent, Rene,Barbier, Geo

, p. 1689 - 1698 (2007/10/02)

A new general synthesis of 4,5-disubstituted 2,4-dihydro-1,2,3-triazole-3-thiones is proposed.These heterocycles are obtained by the action of primary amines, aralhydrazines or aroylhydrazines on the thiosemicarbazones of esters.These last compounds are prepared by action of chlorhydrates of iminoesters on thiosemicarbazide in dimethylformamide.These thiosemicarbazones react also with strong acids, acid anhydrides and chlorides; by thermolysis and they give 2-amino-1,3,4-thiadiazole derivatives.Also, two derivatives of 1,2,4-triazolo-1,3,4-thiadiazole have been prepared.

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