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CAS 38283-38-4

:

N-(4-Acetylphenyl)-2-chloroacetamide

Description:
N-(4-Acetylphenyl)-2-chloroacetamide, with the CAS number 38283-38-4, is an organic compound characterized by its amide functional group, which is derived from the reaction of 4-acetylphenylamine and chloroacetyl chloride. This compound typically appears as a solid at room temperature and is soluble in organic solvents such as ethanol and acetone, but may have limited solubility in water due to its hydrophobic aromatic structure. The presence of the chloroacetyl group imparts reactivity, making it useful in various synthetic applications, including the development of pharmaceuticals and agrochemicals. Its molecular structure features a phenyl ring substituted with an acetyl group, contributing to its potential biological activity. Additionally, the compound may exhibit properties such as antimicrobial or anti-inflammatory effects, although specific biological activities would depend on further empirical studies. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or reactivity associated with the chloroacetamide moiety.
Formula:C10H10ClNO2
InChI:InChI=1S/C10H10ClNO2/c1-7(13)8-2-4-9(5-3-8)12-10(14)6-11/h2-5H,6H2,1H3,(H,12,14)
InChI key:InChIKey=FLMLTMFETZMOHW-UHFFFAOYSA-N
SMILES:N(C(CCl)=O)C1=CC=C(C(C)=O)C=C1
Synonyms:
  • 4′-Acetyl-2-chloroacetanilide
  • 4′-(2-Chloroacetamido)acetophenone
  • N-(4-Acetylphenyl)-2-chloroacetamide
  • Acetamide, N-(4-acetylphenyl)-2-chloro-
  • Acetanilide, 4′-acetyl-2-chloro-
  • TIMTEC-BB SBB003429
  • ASISCHEM V69547
  • N1-(4-Acetylphenyl)-2-chloroacetamide, tech
  • N1-(4-ACETYLPHENYL)-2-CHLOROACETAMIDE
  • 2-chloro-N-(4-ethanoylphenyl)ethanamide
  • See more synonyms
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