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CAS 14949-01-0

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N-[4-(Aminosulfonyl)phenyl]-2-chloroacetamide

Description:
N-[4-(Aminosulfonyl)phenyl]-2-chloroacetamide, also known by its CAS number 14949-01-0, is a chemical compound characterized by its aminosulfonyl and chloroacetamide functional groups. This compound typically appears as a solid and is soluble in polar solvents due to the presence of the sulfonamide group, which enhances its hydrophilicity. It is often utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. The presence of the chloroacetamide moiety suggests potential reactivity, making it a candidate for further chemical modifications. Additionally, the aminosulfonyl group may impart specific biological activities, including antimicrobial or anti-inflammatory properties. As with many sulfonamide derivatives, it may exhibit interactions with biological targets, influencing its pharmacological profile. Safety and handling precautions are essential, as with any chemical compound, to mitigate risks associated with exposure or reactivity. Overall, this compound represents a significant interest in medicinal chemistry and related fields.
Formula:C8H9ClN2O3S
InChI:InChI=1S/C8H9ClN2O3S/c9-5-8(12)11-6-1-3-7(4-2-6)15(10,13)14/h1-4H,5H2,(H,11,12)(H2,10,13,14)
InChI key:InChIKey=WBDDNKFSVVIFOG-UHFFFAOYSA-N
SMILES:S(N)(=O)(=O)C1=CC=C(NC(CCl)=O)C=C1
Synonyms:
  • 2-Chloro-N-(4-sulfamoylphenyl)acetamide
  • Acetamide, N-[4-(aminosulfonyl)phenyl]-2-chloro-
  • Acetanilide, 2-chloro-4′-sulfamoyl-
  • N-[4-(Aminosulfonyl)phenyl]-2-chloroacetamide
  • N<sup>4</sup>-Chloracetylsulfanilamide
  • NSC 525660
  • N4-Chloracetylsulfanilamide
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