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CAS 7463-35-6

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N-(3-Chloro-2-methylphenyl)acetamide

Description:
N-(3-Chloro-2-methylphenyl)acetamide, with the CAS number 7463-35-6, is an organic compound characterized by its amide functional group. It features a chloro-substituted aromatic ring, specifically a 3-chloro-2-methylphenyl moiety, attached to an acetamide group. This compound typically appears as a solid at room temperature and is soluble in organic solvents, reflecting its hydrophobic characteristics due to the aromatic ring. The presence of the chlorine atom introduces unique reactivity and polarity, which can influence its interactions in chemical reactions and biological systems. N-(3-Chloro-2-methylphenyl)acetamide may exhibit various biological activities, making it of interest in pharmaceutical research. Its synthesis generally involves acylation reactions, and it can be analyzed using techniques such as NMR spectroscopy and mass spectrometry to confirm its structure and purity. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken due to potential toxicity or reactivity.
Formula:C9H10ClNO
InChI:InChI=1S/C9H10ClNO/c1-6-8(10)4-3-5-9(6)11-7(2)12/h3-5H,1-2H3,(H,11,12)
InChI key:InChIKey=NALGTKRTIJHBBK-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=C(C)C(Cl)=CC=C1
Synonyms:
  • 2-Methyl-3-chloroacetanilide
  • 3-Chloro-2-methyl-N-acetyl-aniline
  • 3-Chloro-2-methyl-N-acetylaniline
  • Acetamide, N-(3-chloro-2-methylphenyl)-
  • N-(3-chloro-2-methylphenyl)acetamide
  • N-Acetyl-3-chloro-2-methylaniline
  • NSC 404347
  • o-Acetotoluidide, 3′-chloro-
  • 3′-Chloro-2′-methylacetanilide
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