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CAS 101167-02-6

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

Description:
N-[[4-(Aminosulfonyl)phenyl]methyl]-2-chloroacetamide, identified by its CAS number 101167-02-6, is a chemical compound characterized by its amide functional group and the presence of a chloroacetyl moiety. This compound features a phenyl ring substituted with an aminosulfonyl group, which contributes to its potential biological activity. The presence of the chlorine atom in the chloroacetamide structure enhances its reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions. The sulfonamide group is known for its role in medicinal chemistry, particularly in the development of antibacterial agents. This compound may exhibit properties such as solubility in polar solvents and potential interactions with biological targets, which could be of interest in pharmaceutical research. Its structural characteristics suggest that it may participate in hydrogen bonding and other intermolecular interactions, influencing its behavior in biological systems and its utility in drug design. Overall, N-[[4-(Aminosulfonyl)phenyl]methyl]-2-chloroacetamide represents a compound of interest in both synthetic and medicinal chemistry.
Formula:C9H11ClN2O3S
InChI:InChI=1S/C9H11ClN2O3S/c10-5-9(13)12-6-7-1-3-8(4-2-7)16(11,14)15/h1-4H,5-6H2,(H,12,13)(H2,11,14,15)
InChI key:InChIKey=LTZYLTKHHXTVBQ-UHFFFAOYSA-N
SMILES:S(N)(=O)(=O)C1=CC=C(CNC(CCl)=O)C=C1
Synonyms:
  • 2-Chloro-N-(4-sulfamoylbenzyl)acetamide
  • 2-Chloro-N-[(4-sulfamoylphenyl)methyl]acetamide
  • Acetamide, 2-chloro-N-p-sulfamoylbenzyl-
  • N-[[4-(Aminosulfonyl)phenyl]methyl]-2-chloroacetamide
  • acetamide, N-[[4-(aminosulfonyl)phenyl]methyl]-2-chloro-
  • N-[4-(aminosulfonyl)benzyl]-2-chloroacetamide
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