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CAS 14316-16-6

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N-(2-Aminoethyl)-4-methylbenzenesulfonamide

Description:
N-(2-Aminoethyl)-4-methylbenzenesulfonamide, also known as a sulfonamide compound, is characterized by its sulfonamide functional group, which consists of a sulfonyl (SO2) moiety attached to an amine. This compound features a 4-methylbenzene ring, indicating the presence of a methyl group at the para position relative to the sulfonamide group. The aminoethyl side chain contributes to its basicity and potential for forming hydrogen bonds, enhancing its solubility in polar solvents. Typically, sulfonamides exhibit antibacterial properties, as they can inhibit bacterial growth by interfering with folic acid synthesis. The compound may also demonstrate moderate to high stability under standard conditions, although it can be sensitive to extreme pH levels. Its applications may extend to pharmaceuticals, particularly in the development of antimicrobial agents or as intermediates in organic synthesis. Safety data should be consulted to understand its toxicity and handling precautions, as with any chemical substance.
Formula:C9H14N2O2S
InChI:InChI=1S/C9H14N2O2S/c1-8-2-4-9(5-3-8)14(12,13)11-7-6-10/h2-5,11H,6-7,10H2,1H3
InChI key:InChIKey=JATMCAQQSXISOR-UHFFFAOYSA-N
SMILES:S(NCCN)(=O)(=O)C1=CC=C(C)C=C1
Synonyms:
  • 2-[[(4-Methylphenyl)sulfonyl]amino]ethylamine
  • Benzenesulfonamide, N-(2-aminoethyl)-4-methyl-
  • N-(2-Aminoethyl)-4-methylbenzenesulfonamide
  • N-(2-Aminoethyl)-4-toluenesulfonamide
  • N-(2-Aminoethyl)-p-toluenesulfonamide
  • N-(4-Toluenesulfonyl)ethylene-1,2-diamine
  • N-Tosylethylenediamine
  • N-p-Tolylsulfonylethylenediamine
  • NSC 177937
  • p-Toluenesulfonamide, N-(2-aminoethyl)-
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