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"N-(5-amino-[1,3,4]thiadiazole-2-sulfonyl)-N'(-4-methoxy-phenyl)-oxalamide" is a complex organic compound with a molecular formula of C11H10N4O4S2. It features a central oxalamide structure, which is a derivative of oxalic acid amide. The compound is characterized by the presence of a 5-amino-[1,3,4]thiadiazole-2-sulfonyl group, which contributes to its sulfur-containing heterocyclic nature, and a 4-methoxy-phenyl group, indicating the presence of a methoxy substituent on the phenyl ring. This chemical is known for its potential applications in pharmaceuticals and as a building block in the synthesis of various biologically active molecules. Its unique structure, which includes both amine and sulfonyl functionalities, suggests that it may have interesting chemical reactivity and could be involved in a range of chemical transformations.

72304-32-6

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72304-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72304-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,3,0 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 72304-32:
(7*7)+(6*2)+(5*3)+(4*0)+(3*4)+(2*3)+(1*2)=96
96 % 10 = 6
So 72304-32-6 is a valid CAS Registry Number.

72304-32-6Downstream Products

72304-32-6Relevant academic research and scientific papers

INVESTIGATION OF THE KINETICS AND THERMODYNAMIC CHARACTERISTICS OF THE ACYLATION OF SODIUM 2-AMINO-1,3,4-THIADIAZOLE-5-SULFONAMIDATE BY N-ARYLOXAMIC ESTERS IN DIMETHYLFORMAMIDE

Shapovalov, V. A.,Bulada, Zh. P.,Bezuglyi, P. A.,Chernykh, V. P.,Bezuglyi, V. D.

, p. 2276 - 2279 (2007/10/02)

The acylation of sodium 2-amino-1,3,4-thiadiazole-5-sulfonamidate by N-aryloxamic esters in dimethylformamide was investigated by a polarographic method.The obtained data made it possible to establish that the reaction is described by a second-order kinetic equation and takes in two stages with the formation of a complex of the anion of the salt form with the oxamic ester as intermediate product.The kinetic and thermodynamic characteristics of this process were calculated, and the effect of the nature of the solvent in the benzene ring of the ester was investigated.

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