CAS 363-40-6
:N-(2,4,6-trifluorophenyl)acetamide
Description:
N-(2,4,6-trifluorophenyl)acetamide, with the CAS number 363-40-6, is an organic compound characterized by the presence of a trifluorophenyl group attached to an acetamide moiety. This compound features a phenyl ring substituted with three fluorine atoms at the 2, 4, and 6 positions, which significantly influences its chemical properties, including increased electronegativity and potential reactivity. The acetamide functional group contributes to its ability to engage in hydrogen bonding, affecting its solubility and boiling point. Typically, compounds like N-(2,4,6-trifluorophenyl)acetamide exhibit moderate to high stability under standard conditions, although they may be sensitive to strong bases or acids. The trifluoromethyl groups can enhance lipophilicity, making such compounds of interest in pharmaceutical and agrochemical applications. Additionally, the unique electronic properties imparted by the fluorine atoms can influence the compound's biological activity, making it a subject of study in medicinal chemistry. Overall, this compound exemplifies the interplay between structure and reactivity in organic chemistry.
Formula:C8H6F3NO
InChI:InChI=1/C8H6F3NO/c1-4(13)12-8-6(10)2-5(9)3-7(8)11/h2-3H,1H3,(H,12,13)
SMILES:CC(=Nc1c(cc(cc1F)F)F)O
Synonyms:- acetamide, N-(2,4,6-trifluorophenyl)-
- N-(2,4,6-Trifluorophenyl)acetamide
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2',4',6'-Trifluoroacetanilide
CAS:<p>2',4',6'-Trifluoroacetanilide</p>Color and Shape:PowderMolecular weight:189.13g/mol
