3-Trifluoromethyl-1H-indole

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3-Trifluoromethyl-1H-indole Basic information
Product Name:3-Trifluoromethyl-1H-indole
Synonyms:1H-Indole, 3-(trifluoroMethyl)-;3-Trifluoromethyl-1H-indole
CAS:51310-55-5
MF:C9H6F3N
MW:185.15
EINECS:
Product Categories:
Mol File:51310-55-5.mol
3-Trifluoromethyl-1H-indole Structure
3-Trifluoromethyl-1H-indole Chemical Properties
Melting point 109-110 °C
Boiling point 256.7±35.0 °C(Predicted)
density 1.367±0.06 g/cm3(Predicted)
storage temp. 2-8°C
pka15.16±0.30(Predicted)
AppearanceLight yellow to yellow Solid
Safety Information
HS Code 2933998090
MSDS Information
3-Trifluoromethyl-1H-indole Usage And Synthesis
Synthesis
Indole

120-72-9

Sodium trifluoromethanesulfinate

2926-29-6

2-Trifluoromethylindole

51310-54-4

3-TRIFLUOROMETHYL-1H-INDOLE

51310-55-5

GENERAL METHODS: Indole derivative (0.3 mmol, 1.0 eq.), sodium trifluoromethanesulfinate (0.6 mmol, 2.0 eq.), 2-tert-butyl anthraquinone (0.06 mmol, 0.2 eq.), and ammonium carbonate (0.18 mmol, 0.6 eq.) were sequentially added to a quartz reaction tube. Hexafluoroisopropanol (0.075 mmol, 0.25 eq.) and acetonitrile (3 mL, 0.1 M) were subsequently added as solvents. The reaction mixture was exposed to 255 nm UV light for 24 hours. Upon completion of the reaction, the reaction was quenched with water and extracted with dichloromethane or ethyl acetate (3 x 30 mL). The organic phases were combined, dried with anhydrous sodium sulfate, and concentrated under reduced pressure to remove the solvent. Finally, the target products 2-trifluoromethylindole and 3-(trifluoromethyl)-1H-indole were obtained by preparative thin-layer chromatography (TLC) using a suitable solvent system.

References[1] Journal of Fluorine Chemistry, 2018, vol. 214, p. 94 - 100
3-Trifluoromethyl-1H-indole Preparation Products And Raw materials
Raw materialsIndole-->Sodium trifluoromethanesulfinate-->Acetonitrile-->Ammonium carbonate-->1,1,1,3,3,3-Hexafluoro-2-propanol
Tag:3-Trifluoromethyl-1H-indole(51310-55-5) Related Product Information
3-Methyl-2-(trifluoromethyl)-1H-indole 5-Methoxy-2-(trifluoromethyl)-1H-indole 2-TRIFLUOROMETHYL-1H-INDOLE 7-(Trifluoromethyl)indoline-2,3-dione 6-Trifluoromethyl-1H-indole-2-carboxylic acid 1-(4-Chlorobenzoyl)-3-methyl-2-(trifluoromethyl)-1H-indole 2-(Trifluoromethyl)-1H-indole-3-acetic acid 3-(Trifluoromethyl)pyrazole 2-(Trifluoromethyl)-1H-indole-3-acetonitrile 6-(TRIFLUOROMETHYL)-1H-INDOLE 5-(Trifluoromethyl)indole-2-carboxylic acid ethyl ester 5-Trifluoromethyl-1H-indole-2-carboxylic acid ethyl ester 5-bromo-7-(trifluoromethyl)-1H-indole 5-bromo-6-(trifluoromethyl)-1H-indole 5-Trifluoromethyl-1H-indole-2-carboxylic acid 4-(Trifluoromethyl)-1H-indole 4-(Trifluoromethyl)-1H-indole-2,3-dione 7-Chloro-4-(trifluoromethyl)-1H-indole-2-carboxylic acid