N-acetyl-4-(5-methyl-3-phenyl-isoxazol-4-yl)-benzenesulfonamide
$250.00
CAS No.: 198471-06-6
Catalog No.: 194183
Purity: 95%
MF: C18H16N2O4S
MW: 356.403
Storage: 2-8 degree Celsius
SMILES: C(C)(=O)NS(=O)(=O)C1=CC=C(C=C1)C=1C(=NOC1C)C1=CC=CC=C1
Catalog No.: 194183
Purity: 95%
MF: C18H16N2O4S
MW: 356.403
Storage: 2-8 degree Celsius
SMILES: C(C)(=O)NS(=O)(=O)C1=CC=C(C=C1)C=1C(=NOC1C)C1=CC=CC=C1
N-acetyl-4-(5-methyl-3-phenyl-isoxazol-4-yl)-benzenesulfonamide; CAS No.: 198471-06-6; N-acetyl-4-(5-methyl-3-phenyl-isoxazol-4-yl)-benzenesulfonamide. PROPERTIES: N-acetyl-4-(5-methyl-3-phenyl-isoxazol-4-yl)-benzenesulfonamide is a crystalline solid. Its molecular formula is C18H16N2O3S, and the molecular weight is approximately 356.40 g/mol. The compound has a melting point of approximately 170-172 C. It is slightly soluble in water but dissolves well in organic solvents such as methanol and dimethylformamide. For proper storage, it should be kept in a sealed container at room temperature, away from heat and direct sunlight. As a compound containing a sulfonamide group and an isoxazole ring, it may exhibit certain reactivity and stability. When handling it, protective gloves and eye protection should be worn. In case of accidental ingestion, medical attention should be sought immediately. APPLICATIONS: In organic synthesis, N-acetyl-4-(5-methyl-3-phenyl-isoxazol-4-yl)-benzenesulfonamide serves as a valuable intermediate. The sulfonamide group can undergo various reactions such as hydrolysis and acylation. The isoxazole ring provides opportunities for further functionalization. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For instance, in the development of certain anti-inflammatory drugs, the structure of N-acetyl-4-(5-methyl-3-phenyl-isoxazol-4-yl)-benzenesulfonamide can be modified to enhance the drug's efficacy and reduce side effects (as described in medicinal chemistry research articles). Additionally, in the field of chemical research, it can be used as a starting material for the synthesis of novel organic compounds with potential applications in catalysis and sensing (as mentioned in organic chemistry research papers).
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