N-((3-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)propionamide
$300.00
CAS No.: 1709956-89-7
Catalog No.: 194203
Purity: 95%
MF: C19H18N2O4S
MW: 370.43
Storage: 2-8 degree Celsius
SMILES: CC1=C(C(=NO1)C1=CC=CC=C1)C=1C=C(C=CC1)S(=O)(=O)NC(CC)=O
Catalog No.: 194203
Purity: 95%
MF: C19H18N2O4S
MW: 370.43
Storage: 2-8 degree Celsius
SMILES: CC1=C(C(=NO1)C1=CC=CC=C1)C=1C=C(C=CC1)S(=O)(=O)NC(CC)=O
N-((3-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)propionamide; CAS No.: 1709956-89-7; N-((3-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)propionamide. PROPERTIES: N-((3-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)propionamide is a crystalline solid. Its molecular formula is C17H16N2O3S, and the molecular weight is approximately 324.39 g/mol. The compound has a melting point of approximately 150-152 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 sulfonyl group, an amide 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 contact with skin or eyes, immediate rinsing with water is necessary. APPLICATIONS: In organic synthesis, N-((3-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)propionamide serves as a versatile intermediate. The sulfonyl group can undergo various reactions such as hydrolysis and alkylation. The amide group can participate in acylation and amidation reactions. In the pharmaceutical industry, derivatives of this compound can be explored as potential drug candidates. For instance, in the development of certain antimicrobial agents, the structure of N-((3-(5-methyl-3-phenylisoxazol-4-yl)phenyl)sulfonyl)propionamide can be modified to enhance the drug's antimicrobial activity and selectivity (as reported in medicinal chemistry journals). 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 noted in organic chemistry research papers).
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