Basic information Safety Supplier Related

4-(TRIFLUOROMETHYL)-1H-INDOLE

Basic information Safety Supplier Related

4-(TRIFLUOROMETHYL)-1H-INDOLE Basic information

Product Name:
4-(TRIFLUOROMETHYL)-1H-INDOLE
Synonyms:
  • 4-(TRIFLUOROMETHYL)-1H-INDOLE
  • 4-(Trifluoromethyl)-indole
  • 1H-Indole, 4-(trifluoroMethyl)-
  • 4-(Trifluoromethyl)indole,97%
CAS:
128562-95-8
MF:
C9H6F3N
MW:
185.15
Mol File:
128562-95-8.mol
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4-(TRIFLUOROMETHYL)-1H-INDOLE Chemical Properties

Boiling point:
256.7±35.0℃ (760 Torr)
Density 
1.367±0.06 g/cm3 (20 ºC 760 Torr)
Flash point:
109.0±25.9℃
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
pka
15.59±0.30(Predicted)
form 
Solid
Appearance
Brown to black Liquid
CAS DataBase Reference
128562-95-8
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Safety Information

HS Code 
2933998090
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4-(TRIFLUOROMETHYL)-1H-INDOLE Usage And Synthesis

Synthesis

905274-06-8

128562-95-8

Step 2. Synthesis of 4-trifluoromethyl-1H-indole: Dimethyl-[2-(2-nitro-6-trifluoromethyl-phenyl)-vinyl]-amine (6.3 g, 24 mmol) was dissolved in acetic acid (150 mL) and iron powder (4.3 g, 77 mmol) was added. The reaction mixture was heated to reflux and kept overnight under nitrogen protection. After completion of the reaction, it was cooled to room temperature, the reaction mixture was diluted with 2.0 M hydrochloric acid and the aqueous phase was extracted with ethyl acetate. The organic layer was neutralized with saturated potassium carbonate solution and extracted again. Subsequently, the organic layer was washed sequentially with sodium bicarbonate solution and sodium chloride solution. Finally, the organic layer was dried with magnesium sulfate and concentrated to give 4-trifluoromethyl-1H-indole (4.5 g, 100% yield).

References

[1] Patent: WO2008/60998, 2008, A1. Location in patent: Page/Page column 35-36
[2] Bioscience, Biotechnology and Biochemistry, 2008, vol. 72, # 8, p. 2025 - 2033
[3] Patent: US2013/274253, 2013, A1. Location in patent: Paragraph 2944-2945

4-(TRIFLUOROMETHYL)-1H-INDOLESupplier

Carbott PharmTech Inc.
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