Product Name:N-(5-Methylisoxazol-3-yl)benzenesulfonamide

IUPAC Name:N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide

CAS:13053-79-7
Molecular Formula:C10H10N2O3S
Purity:97%
Catalog Number:CM493261
Molecular Weight:238.26

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Product Details

CAS NO:13053-79-7
Molecular Formula:C10H10N2O3S
Melting Point:-
Smiles Code:O=S(C1=CC=CC=C1)(NC2=NOC(C)=C2)=O
Density:
Catalog Number:CM493261
Molecular Weight:238.26
Boiling Point:
MDL No:MFCD00447814
Storage:Sealed in dry,Room Temperature

Category Infos

Isoxazoles
Isoxazole is a liquid heterocyclic compound C3H3NO isomeric with oxazole and having a penetrating odor like that of pyridine. Isoxazoles belong to an important class of five-membered aromatic heterocycles containing two electronegative heteroatoms, nitrogen and oxygen, in a 1,2-relationship and three regular sp2 carbon atoms. These molecules are found to be key components in various synthetic products in daily use and also present as a pharmacophore essential for biological activity in many drugs and bioactive natural products. In addition, isoxazoles have demonstrated their ability to exhibit hydrogen bond donor/acceptor interactions with a variety of enzymes and receptors.

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Product Other Information

Product Overview N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamide, also known as Sulfamethoxazole, is a synthetic sulfonamide antibiotic commonly used in medical practice.
Synthesis Method N-(5-methyl-1,2-oxazol-3-yl)benzenesulfonamidezole is synthesized in a three-step process. First, 5-methyl-1,2-oxazol-3-ylbenzene is reacted with chlorosulfonic acid to form 5-methyl-1,2-oxazol-3-ylbenzenesulfonyl chloride. This is then reacted with sodium methoxide to form 5-methyl-1,2-oxazol-3-ylbenzenesulfonamide. Finally, the sulfonamide is reacted with sodium hydroxide to form the final product, sulfamethoxazole.
Chemical Properties It is relatively inexpensive and can be easily synthesized. 
Synthesis and Application It has been used in a variety of biological and medical studies, including studies of its pharmacokinetics, pharmacodynamics, and toxicity. It has also been used to study the mechanism of action of antibiotics, as well as the biochemical and physiological effects of antibiotics.
Future Directions It could be used to study the mechanisms of action of other antibiotics, as well as to develop new antibiotics. Additionally, it could be used to study the biochemical and physiological effects of antibiotics, and to develop new treatments for bacterial and fungal infections. It could also be used to study the effects of drug interactions, as well as to develop new drugs with improved pharmacokinetics and pharmacodynamics. Finally, it could be used to develop new treatments for inflammatory and immunological diseases.