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4-(2-(3-methyl-5-oxoisoxazol-4(5H)-ylidine)hydrazinyl)benzenesulfonamide is a complex organic compound with the molecular formula C10H11N5O4S. It is characterized by a benzene ring with a sulfonamide group attached to the 4-position, and a hydrazinyl group at the 2-position, which is further connected to a 3-methyl-5-oxoisoxazole ring. 4-(2-(3-methyl-5-oxoisoxazol-4(5H)-ylidine)hydrazinyl)benzenesulfonamide is known for its potential applications in pharmaceutical research, particularly as an intermediate in the synthesis of various drugs. Its structure provides a foundation for exploring its chemical properties and reactivity, which can be crucial in the development of new therapeutic agents.

5669-72-7

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5669-72-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5669-72-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5669-72:
(6*5)+(5*6)+(4*6)+(3*9)+(2*7)+(1*2)=127
127 % 10 = 7
So 5669-72-7 is a valid CAS Registry Number.

5669-72-7Downstream Products

5669-72-7Relevant academic research and scientific papers

Aqueous phase synthesis, crystal structure and antimicrobial activity of 4-(substituted phenylazo)-3-methyl-4H-isoxazol-5-one azo dyes

Banpurkar, Anita R.,Wazalwar, Sachin S.,Perdih, Franc

, p. 249 - 257 (2018/09/06)

3-Methyl-4H-isoxazol-5-one was synthesized at room temperature by simple stirring method from ethyl acetoacetate and hydroxylamine hydrochloride in aqueous medium and coupled with diazotized substituted amine to form series of 4-(substituted phenylazo)-3-methyl-4H-isoxazol-5-ones through green chemistry. All the compounds formed were characterized by IR, 1H and 13C NMR spectroscopy, MS and elemental analysis. Crystal structure of novel 4-(4-fluorophenylazo)-3-methyl-4H-isoxazol-5-one was determined by the X-ray diffraction. Antibacterial and antifungal activity was studied against Escherichia coli, Pseudomonas aeruginosa, Staphylococcus aureus, Staphylococcus pyogenus and Candida albicans, Aspergillus niger, Aspergillus clavatus, respectively. All synthesized compounds were found to be active against a gram-positive bacterium Staphylococcus aureus. Two compounds showed antifungal activity against Candida albicans close to standard greseofulvin.

Synthesis and antibacterial activity of some heterocyclic derivatives of sulfanilamide

Subudhi,Ghosh

, p. 455 - 459 (2012/11/07)

Considering the promising antimicrobial potential of carbonic anhydrase inhibitors and heterocyclic compounds some heterocyclic derivatives of sulfanilamide (2a-e) were synthesized. The diazotisation of sulfanilamide followed by substitution with ethylace

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