CAS 5611-64-3

6-chloro-2-methyl-3-[(prop-2-en-1-ylsulfanyl)methyl]-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide

Description:

6-Chloro-2-methyl-3-[(prop-2-en-1-ylsulfanyl)methyl]-3,4-dihydro-2H-1,2,4-benzothiadiazine-7-sulfonamide 1,1-dioxide, with CAS number 5611-64-3, is a chemical compound characterized by its complex structure, which includes a benzothiadiazine core. This compound features a sulfonamide functional group, which is known for its biological activity, particularly in medicinal chemistry. The presence of a chlorine atom and a methyl group contributes to its reactivity and potential pharmacological properties. The prop-2-en-1-ylsulfanyl group introduces additional reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions. The compound's dihydro form indicates it has a saturated ring structure, which may influence its stability and solubility in different solvents. Overall, this compound's unique structural features suggest potential applications in pharmaceuticals, particularly in the development of new therapeutic agents. However, specific biological activities and safety profiles would require further investigation through experimental studies.

Formula: C₁₂H₁₆ClN₃O₄S₃

InChI: InChI=1/C12H16ClN3O4S3/c1-3-4-21-7-12-15-9-5-8(13)10(22(14,17)18)6-11(9)23(19,20)16(12)2/h3,5-6,12,15H,1,4,7H2,2H3,(H2,14,17,18)

Synonyms:

• 2H-1,2,4-Benzothiadiazine-7-sulfonamide, 6-chloro-3,4-dihydro-2-methyl-3-[(2-propenylthio)methyl]-, 1,1-dioxide

Methalthiazide

CAS: 5611-64-3

Methalthiazide enhances the activity of natural agonists of AMPA receptors and can be utilized in schizophrenia research.

Formula: C₁₂H₁₆ClN₃O₄S₃

Color and Shape: Solid

Molecular weight: 397.92

Ref: TM-T203373