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CAS 6590-65-4

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N-(2-Formylphenyl)-4-methylbenzenesulfonamide

Description:
N-(2-Formylphenyl)-4-methylbenzenesulfonamide, with the CAS number 6590-65-4, is an organic compound characterized by its sulfonamide functional group, which is known for its antibacterial properties. This compound features a sulfonamide moiety attached to a phenyl ring that is further substituted with a formyl group and a methyl group. The presence of the formyl group indicates that it can participate in various chemical reactions, such as condensation and reduction, making it a versatile intermediate in organic synthesis. The sulfonamide group contributes to its potential biological activity, as sulfonamides are often used in pharmaceuticals. The compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the presence of the sulfonamide group. Its molecular structure suggests that it may have specific interactions with biological targets, which could be of interest in medicinal chemistry. Overall, N-(2-Formylphenyl)-4-methylbenzenesulfonamide is a compound of interest for both its chemical properties and potential applications in drug development.
Formula:C14H13NO3S
InChI:InChI=1S/C14H13NO3S/c1-11-6-8-13(9-7-11)19(17,18)15-14-5-3-2-4-12(14)10-16/h2-10,15H,1H3
InChI key:InChIKey=QLQGABDYGHEFOM-UHFFFAOYSA-N
SMILES:S(NC1=C(C=O)C=CC=C1)(=O)(=O)C2=CC=C(C)C=C2
Synonyms:
  • 2-(N-Tosylamino)benzaldehyde
  • 2-(Tosylamino)benzaldehyde
  • 2-Formyl-N-tosylaniline
  • 2-[[(4-Tolyl)sulfonyl]amino]benzaldehyde
  • Benzenesulfonamide, N-(2-formylphenyl)-4-methyl-
  • N-(2-Formylphenyl)-4-toluenesulfonamide
  • N-(2-Formylphenyl)-p-toluenesulfonamide
  • NSC 120186
  • o-Tosylaminobenzaldehyde
  • p-Toluenesulfonanilide, 2′-formyl-
  • N-(2-Formylphenyl)-4-methylbenzenesulfonamide
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