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CAS 220227-80-5

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2,4,6-Trifluorophenylacetonitrile

Description:
2,4,6-Trifluorophenylacetonitrile is an organic compound characterized by its trifluoromethyl-substituted phenyl group and a nitrile functional group. It features a phenyl ring with three fluorine atoms positioned at the 2, 4, and 6 positions, which significantly influences its chemical properties, including increased electronegativity and potential reactivity. The acetonitrile moiety contributes to its polar nature, making it soluble in polar solvents. This compound is often utilized in synthetic organic chemistry, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to serve as an intermediate in various chemical reactions. The presence of fluorine atoms enhances its stability and lipophilicity, which can affect its biological activity. Additionally, 2,4,6-Trifluorophenylacetonitrile may exhibit unique spectral properties, making it useful in analytical applications. Safety data should be consulted, as fluorinated compounds can pose specific health and environmental risks. Overall, this compound exemplifies the importance of halogenated derivatives in modern chemical synthesis and applications.
Formula:C8H4F3N
InChI:InChI=1/C8H4F3N/c9-5-3-7(10)6(1-2-12)8(11)4-5/h3-4H,1H2
SMILES:C(C#N)c1c(cc(cc1F)F)F
Synonyms:
  • (2,4,6-Trifluorophenyl)acetonitrile
  • 2,4,6-Trifluorobenzeneacetonitrile
  • Benzeneacetonitrile, 2,4,6-trifluoro-
  • Nc1R Bf Df Ff
  • 2,4,6-Trifluorobenzylcyanide
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