3-(TRIFLUOROACETYL)INDOLE

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Company Name: Shenzhen Nexconn Pharmatechs Ltd
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Products Intro: Product Name:3-(Trifluoroacetyl)indole
CAS:14618-45-2
Purity:98% Package:1KG;10KG;50KG
Company Name: Alchem Pharmtech,Inc.
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Products Intro: Product Name:3-(Trifluoroacetyl)indole
CAS:14618-45-2
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-02658
Company Name: CONIER CHEM AND PHARMA LIMITED
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Products Intro: Product Name:2,2,2-trifluoro-1-(1h-indol-3-yl)-1-ethanone
CAS:14618-45-2
Purity:99% Package:1kg
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Products Intro: Product Name:3-(TRIFLUOROACETYL)INDOLE
CAS:14618-45-2
Purity:99% Package:1KG;1USD
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Products Intro: Product Name:3-(Trifluoroacetyl)indole
CAS:14618-45-2

3-(TRIFLUOROACETYL)INDOLE manufacturers

3-(TRIFLUOROACETYL)INDOLE Basic information
Product Name:3-(TRIFLUOROACETYL)INDOLE
Synonyms:2,2,2-TRIFLUORO-1-(1H-INDOL-3-YL)-1-ETHANONE;3-(TRIFLUOROACETYL)INDOLE;3-(TRIFLUOROACETYL)INDOLE 99%;3-Indolyl trifluoromethyl ketone;Ethanone, 2,2,2-trifluoro-1-(1H-indol-3-yl)-
CAS:14618-45-2
MF:C10H6F3NO
MW:213.16
EINECS:
Product Categories:Biochemistry;Indoles;Plant Growth Regulators;Plant Growth Trgulators (Others);Simple Indoles;Building Blocks;Heterocyclic Building Blocks
Mol File:14618-45-2.mol
3-(TRIFLUOROACETYL)INDOLE Structure
3-(TRIFLUOROACETYL)INDOLE Chemical Properties
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
pka14.31±0.30(Predicted)
form Solid
color White to Almost white
CAS DataBase Reference14618-45-2(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36
WGK Germany 3
HazardClass IRRITANT
HS Code 2933992000
MSDS Information
ProviderLanguage
SigmaAldrich English
3-(TRIFLUOROACETYL)INDOLE Usage And Synthesis
UsesReactant 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.
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
General Description3-(Trifluoroacetyl)indole is a heterocyclic trifluoromethyl ketone. One of the methods reported for its synthesis is by the reaction of indole with trifluoroacetic anhydride.
3-(TRIFLUOROACETYL)INDOLE Preparation Products And Raw materials
Preparation Products5-Acetylindole
Tag:3-(TRIFLUOROACETYL)INDOLE(14618-45-2) Related Product Information
1-Methyl-3-(trifluoroacetyl)-1H-indole 1-(1-ETHYL-1H-INDOL-3-YL)-2,2,2-TRIFLUORO-1-ETHANONE 3-(TRIFLUOROACETYL)INDOLE 2,2,2-TRIFLUORO-1-[1-(METHYLSULFONYL)-1H-INDOL-3-YL]-1-ETHANONE 2,2,2-trifluoro-1-(5-nitro-1H-indol-3-yl)ethanone 2,2,2-TRIFLUORO-1-(2-PHENYL-1H-INDOL-3-YL)-1-ETHANONE 1-(1-BENZYL-1H-INDOL-3-YL)-2,2,2-TRIFLUORO-1-ETHANONE