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What is the sodium N-(5-methylisoxazol-3-yl)sulphanilamidate ?

sodium N-(5-methylisoxazol-3-yl)sulphanilamidate is , while it's Molecular Formula is C10H11N3NaO3S. Used in Pharmaceutical Research:
Sodium N-(5-methylisoxazol-3-yl)sulphanilamidate is used as a potential antibacterial agent for pharmaceutical research. Its structure, which includes a sulphanilamide moiety, suggests that it may exhibit antibacterial activities, making it a candidate for further investigation in the development of new antimicrobial drugs.
Used in Chemical Synthesis:
In the chemical industry, sodium N-(5-methylisoxazol-3-yl)sulphanilamidate may serve as an intermediate or a building block in the synthesis of more complex molecules. Its unique structure could be utilized in the creation of novel compounds with potential applications in various fields, such as materials science or medicinal chemistry.
Used in Material Science:
Sodium N-(5-methylisoxazol-3-yl)sulphanilamidate could be explored for its potential applications in material science. sodium N-(5-methylisoxazol-3-yl)sulphanilamidate's structure and properties might contribute to the development of new materials with specific characteristics, such as improved stability, reactivity, or selectivity in certain chemical processes.

What is the CAS number for sodium N-(5-methylisoxazol-3-yl)sulphanilamidate ?

The CAS number of sodium N-(5-methylisoxazol-3-yl)sulphanilamidate is 4563-84-2.

More information of sodium N-(5-methylisoxazol-3-yl)sulphanilamidate 4563-84-2 are:

What is sodium N-(5-methylisoxazol-3-yl)sulphanilamidate (4563-84-2) used for?

Sodium N-(5-methylisoxazol-3-yl)sulphanilamidate is a complex chemical compound that combines a metallic sodium atom with an organic component. This organic part features a 5-methylisoxazol-3-yl group and a sulphanilamidate moiety. The isoxazole ring in its structure is substituted with a methyl group at the fifth position, and the sulphanilamide portion is a sulfonamide derivative, which is known for its antibacterial properties. sodium N-(5-methylisoxazol-3-yl)sulphanilamidate may hold potential for pharmaceutical research, particularly in the development of new antibacterial agents. However, due to the lack of extensive information on its properties, applications, or safety profile, it appears to be a less commonly studied or utilized substance.

InChI:InChI=1/C10H10N3O3S.Na/c1-7-6-10(12-16-7)13-17(14,15)9-4-2-8(11)3-5-9;/h2-6H,11H2,1H3;/q-1;+1

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