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CAS 78521-39-8

:

6-[[(4-Methylphenyl)sulfonyl]amino]hexanoic acid

Description:
6-[[(4-Methylphenyl)sulfonyl]amino]hexanoic acid, with the CAS number 78521-39-8, is an organic compound characterized by its sulfonamide functional group and a hexanoic acid backbone. This compound features a 4-methylphenyl group attached to a sulfonyl moiety, which contributes to its chemical reactivity and solubility properties. The presence of the amino group enhances its potential for hydrogen bonding, making it more soluble in polar solvents. The hexanoic acid chain provides hydrophobic characteristics, influencing its interaction with biological membranes. This compound may exhibit biological activity, potentially serving as a pharmaceutical intermediate or a research chemical. Its structural features suggest it could participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Additionally, the sulfonamide group is known for its role in medicinal chemistry, particularly in the development of antibacterial agents. Overall, 6-[[(4-Methylphenyl)sulfonyl]amino]hexanoic acid is a versatile compound with applications in both research and industry, particularly in the fields of organic synthesis and drug development.
Formula:C13H19NO4S
InChI:InChI=1/C13H19NO4S/c1-11-6-8-12(9-7-11)19(17,18)14-10-4-2-3-5-13(15)16/h6-9,14H,2-5,10H2,1H3,(H,15,16)
InChI key:InChIKey=GLKZGJGPYOFPKV-UHFFFAOYSA-N
SMILES:S(NCCCCCC(O)=O)(=O)(=O)C1=CC=C(C)C=C1
Synonyms:
  • 6-[(4-Methylbenzenesulfonyl)amino]caproic acid
  • 6-{[(4-Methylphenyl)Sulfonyl]Amino}Hexanoic Acid
  • Hexanoic acid, 6-(((4-methylphenyl)sulfonyl)amino)-
  • Hexanoic acid, 6-p-toluenesulfonamido-
  • NSC 38047
  • 6-(((4-Methylphenyl)sulphonyl)amino)hexanoic acid
  • Arylsulphonylamino carboxylic acid
  • 6-(Toluene-4-sulfonylamino)-hexanoic acid
  • 6-(4-methylphenylsulfonamido)hexanoic acid
  • Einecs 278-934-5
  • See more synonyms
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