3-(2,2,2-Trifluoroacetyl)benzonitrile, with the CAS number 23568-85-6, is an organic compound characterized by the presence of both a nitrile and a trifluoroacetyl functional group. This compound features a benzene ring substituted at the meta position with a benzonitrile group, which contributes to its aromatic properties and potential reactivity. The trifluoroacetyl group enhances the compound's electrophilicity due to the strong electron-withdrawing nature of the trifluoromethyl group, making it useful in various synthetic applications. The presence of fluorine atoms increases the compound's lipophilicity and may influence its biological activity. Additionally, the compound may exhibit unique physical properties, such as increased stability and altered solubility in organic solvents compared to its non-fluorinated counterparts. Its applications can range from pharmaceuticals to agrochemicals, where the trifluoroacetyl moiety can play a crucial role in modulating biological interactions. Overall, 3-(2,2,2-trifluoroacetyl)benzonitrile is a versatile compound with significant implications in chemical synthesis and research.

3-(2,2,2-trifluoroacetyl)benzonitrile

23568-85-6: 3-(2,2,2-Trifluoroacetyl)benzonitrile, with the CAS number 23568-85-6, is an organic compound characterized by the presence of both a nitrile and a trifluoroacetyl functional group. This compound features a benzene ring substituted at the meta position with a benzonitrile group, which contributes to its aromatic properties and potential reactivity. The trifluoroacetyl group enhances the compound's electrophilicity due to the strong electron-withdrawing nature of the trifluoromethyl group, making it useful in various synthetic applications. The presence of fluorine atoms increases the compound's lipophilicity and may influence its biological activity. Additionally, the compound may exhibit unique physical properties, such as increased stability and altered solubility in organic solvents compared to its non-fluorinated counterparts. Its applications can range from pharmaceuticals to agrochemicals, where the trifluoroacetyl moiety can play a crucial role in modulating biological interactions. Overall, 3-(2,2,2-trifluoroacetyl)benzonitrile is a versatile compound with significant implications in chemical synthesis and research.

CAS 23568-85-6

3-(2,2,2-trifluoroacetyl)benzonitrile

3-(2,2,2-Trifluoroacetyl)benzonitrile

Ref: IN-DA002NON

3′-Cyano-2,2,2-trifluoroacetophenone

Ref: 10-F207009

3-(Trifluoroacetyl)Benzonitrile

Ref: TR-T220615