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4-[(3,5-dimethyl-1H-pyrazol-4-yl)diazenyl]-N-(pyrimidin-2-yl)benzenesulfonamide is a complex organic compound with the molecular formula C16H16N6O2S. It is characterized by a benzene ring with a sulfonamide group attached to the 4-position, a pyrimidin-2-yl group at the nitrogen, and a 3,5-dimethyl-1H-pyrazol-4-yl diazenyl group at the same position. 4-[(3,5-dimethyl-1H-pyrazol-4-yl)diazenyl]-N-(pyrimidin-2-yl)benzenesulfonamide is known for its potential applications in pharmaceuticals and chemical research, particularly in the development of new drugs and the study of molecular interactions. Its structure provides a foundation for understanding its reactivity and potential therapeutic properties.

978-73-4

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978-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 978-73-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,7 and 8 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 978-73:
(5*9)+(4*7)+(3*8)+(2*7)+(1*3)=114
114 % 10 = 4
So 978-73-4 is a valid CAS Registry Number.

978-73-4Downstream Products

978-73-4Relevant academic research and scientific papers

Pyrazole and Nicotinonitrile Derivatives Synthesized from Sulfa Drugs, and Their Antibacterial Activity

El-Sayed,Moustafa,Fadda,Abd El-Rahman

, p. 339 - 347 (2019/04/13)

Utility of sulfadiazine and sulfaguanidine in synthesis of new series of pyrazoles and 2-pyridones is described. Diazotization of sulfadiazine that results in formation of diazonium salt 2 followed by coupling of the latter with active methylene compounds

Polysubstituted pyrazoles. Part 2: Sulphonamidophenylhydrazone-2-pyrazolin-4-ones and sulphonamidophenylazopyrazoles as potential anticancer agents.

Soliman,Shafik

, p. 436 - 439 (2007/10/08)

The synthesis of some new derivatives of 1-[4-nitrophenyl]-5-[4-substituted sulphonamidophenylhydrazono]-2-pyrazolin-4-ones and 3,5-dimethyl-4-[4-substituted sulphonamidophenylazo]-pyrazoles is described. Bromination of ethyl 2-[nitrophenylhydrazono]-3-oxobutyrates in dry benzene afforded the 4-bromo derivatives which upon cyclization gave high yields of the 4-hydroxpyrazoles. Many other new intermediates were prepared and the results of the UV and IR spectral studies are discussed.

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