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CAS 392-16-5

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N-(2,6-Dichloro-4-fluorophenyl)acetamide

Description:
N-(2,6-Dichloro-4-fluorophenyl)acetamide, with the CAS number 392-16-5, is an organic compound characterized by its amide functional group. It features a phenyl ring substituted with two chlorine atoms and one fluorine atom, contributing to its unique chemical properties. The presence of these halogen substituents typically enhances the compound's lipophilicity and may influence its biological activity. This compound is often studied for its potential applications in pharmaceuticals, particularly in the development of agrochemicals or medicinal agents. Its molecular structure suggests that it may exhibit specific interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the halogen substituents. As with many organic compounds, safety and handling precautions are essential, as it may pose health risks if not managed properly. Overall, N-(2,6-Dichloro-4-fluorophenyl)acetamide represents a significant compound in the realm of synthetic organic chemistry.
Formula:C8H6Cl2FNO
InChI:InChI=1S/C8H6Cl2FNO/c1-4(13)12-8-6(9)2-5(11)3-7(8)10/h2-3H,1H3,(H,12,13)
InChI key:InChIKey=CXYGMKNUTOTBGM-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=C(Cl)C=C(F)C=C1Cl
Synonyms:
  • Acetanilide, 2′,6′-dichloro-4′-fluoro-
  • acetamide, N-(2,6-dichloro-4-fluorophenyl)-
  • N-(2,6-Dichloro-4-fluorophenyl)acetamide
  • N-(2,6-Dichloro-4-fluorophenyl)acetamide
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