2-Chloro-4-methylthiazole-5-sulfonamide is a chemical compound characterized by its thiazole ring structure, which incorporates a chlorine atom and a methyl group at specific positions. This compound features a sulfonamide functional group, which is known for its antibacterial properties. The presence of the chlorine atom contributes to its reactivity and potential biological activity. The thiazole ring is a five-membered heterocyclic structure containing both sulfur and nitrogen, which enhances the compound's pharmacological profile. Typically, sulfonamides are utilized in medicinal chemistry for their ability to inhibit bacterial growth by interfering with folic acid synthesis. The specific arrangement of substituents in 2-Chloro-4-methylthiazole-5-sulfonamide may influence its solubility, stability, and interaction with biological targets. Overall, this compound is of interest in pharmaceutical research, particularly in the development of new antimicrobial agents. As with many sulfonamides, safety and toxicity profiles are essential considerations in its application.

2-Chloro-4-methylthiazole-5-sulfonamide

348086-67-9: 2-Chloro-4-methyl-1,3-thiazole-5-sulfonamide, 5-Thiazolesulfonamide, 2-Chloro-4-Methyl-

2-Chloro-4-Methyl-5-Thiazolesulfonamide

2-Chloro-4-methylthiazole-5-sulfonic acid amide

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CAS 348086-67-9: 2-Chloro-4-methylthiazole-5-sulfonamide

2-Chloro-4-methylthiazole-5-sulfonamide

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2-Chloro-4-Methyl-5-Thiazolesulfonamide

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2-Chloro-4-methylthiazole-5-sulfonic acid amide

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2-Chloro-4-methylthiazole-5-sulfonic acid amide

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2-Chloro-4-methylthiazole-5-sulfonamide

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