3-(Trifluoroacetyl)indole is an organic compound characterized by the presence of an indole ring substituted at the 3-position with a trifluoroacetyl group. This compound features a bicyclic structure consisting of a fused benzene and pyrrole ring, which is typical of indole derivatives. The trifluoroacetyl group introduces significant electronegativity due to the three fluorine atoms, influencing the compound's reactivity and polarity. As a result, 3-(Trifluoroacetyl)indole exhibits unique chemical properties, including potential applications in medicinal chemistry and material science. It may participate in various chemical reactions, such as nucleophilic substitutions or electrophilic aromatic substitutions, due to the electron-withdrawing nature of the trifluoroacetyl moiety. Additionally, the compound's solubility and stability can be affected by the presence of the trifluoroacetyl group, making it of interest for further studies in synthesis and reactivity. Overall, 3-(Trifluoroacetyl)indole serves as a valuable building block in organic synthesis and has implications in the development of pharmaceuticals and agrochemicals.

3-(Trifluoroacetyl)indole

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Ethanone, 2,2,2-trifluoro-1-(1H-indol-3-yl)-

2,2,2-Trifluoro-1-(1H-indol-3-yl)ethanone is a chemical reagent that is used in the synthesis of medicines. It has been shown to be a good solvent for reactions involving trifluoroacetic acid and chloride. It is also an operational solvent for reactions involving sulfoxide and dialkylamides. 2,2,2-Trifluoro-1-(1H-indol-3-yl)ethanone can be evaporated at reflux temperature and then distilled to remove the trifluoroacetyl group.

CAS 14618-45-2: 3-(Trifluoroacetyl)indole

Ethanone, 2,2,2-trifluoro-1-(1H-indol-3-yl)-

Ref: IN-DA001DSB

2,2,2-trifluoro-1-(1h-indol-3-yl)ethanone

Ref: 3D-FT105493

3-(Trifluoroacetyl)indole

Ref: 54-PC408009

3-(Trifluoroacetyl)indole

Ref: 3B-T1809

3-(Trifluoroacetyl)indole

Ref: 10-F008804