14618-45-2

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14618-45-2 Structure

Identification	More
[Name] 3-(TRIFLUOROACETYL)INDOLE
[CAS] 14618-45-2
[Synonyms] 2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)-1-ETHANONE 3-(TRIFLUOROACETYL)INDOLE 3-(TRIFLUOROACETYL)INDOLE 99%
[Molecular Formula] C10H6F3NO
[MDL Number] MFCD00182114
[Molecular Weight] 213.16
[MOL File] 14618-45-2.mol

Chemical Properties	Back Directory
[Melting point ] 211-214 °C(lit.)
[Boiling point ] 308.6±37.0 °C(Predicted)
[density ] 1.423±0.06 g/cm3(Predicted)
[storage temp. ] Sealed in dry,Room Temperature
[form ] Solid
[pka] 14.31±0.30(Predicted)
[color ] White to Almost white
[CAS DataBase Reference] 14618-45-2(CAS DataBase Reference)

Safety Data	Back Directory
[Hazard Codes ] Xi
[Risk Statements ] R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ] S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice . S36:Wear suitable protective clothing .
[WGK Germany ] 3
[HazardClass ] IRRITANT
[HS Code ] 2933992000

Hazard Information	Back Directory
[Uses] Reactant for enantioselective synthesis of indoles via palladium-catalyzed kinetic asymmetrical alkylation Reactant for preparation of N-pyridinyl indolecarboxamides via amidation of aminopyridine derivatives. with indolecarboxylic acid Reactant for preparation of mast cell tryptase inhibitors, starting from indoles; using amidation as the key step Reactant for formation of Michael adducts via Baylis-Hillman reaction Reactant for preparation of indolecarboxamides via haloform cleavage of (trifluoroacetyl)indole with lithium dialkylamides
[Uses] Reactant for enantioselective synthesis of indoles via palladium-catalyzed kinetic asymmetrical alkylation. Reactant for preparation of N-pyridinyl indolecarboxamides via amidation of aminopyridine derivatives. with indolecarboxylic acid 2 Reactant for preparation of mast cell tryptase inhibitors, starting from indoles; using amidation as the key step 3 Reactant for formation of Michael adducts via Baylis-Hillman reaction 4 Reactant for preparation of indolecarboxamides via haloform cleavage of (trifluoroacetyl)indole with lithium dialkylamides.
[General Description] 3-(Trifluoroacetyl)indole is a heterocyclic trifluoromethyl ketone. One of the methods reported for its synthesis is by the reaction of indole with trifluoroacetic anhydride.

Spectrum Detail	Back Directory
[Spectrum Detail] 3-(TRIFLUOROACETYL)INDOLE(14618-45-2)¹HNMR 3-(TRIFLUOROACETYL)INDOLE(14618-45-2)FT-IR 3-(TRIFLUOROACETYL)INDOLE(14618-45-2)IR

Well-known Reagent Company Product Information	Back Directory
[Sigma Aldrich] 14618-45-2(sigmaaldrich)
[TCI AMERICA] 3-(Trifluoroacetyl)indole(14618-45-2)

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14618-45-2

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