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4-(TRIFLUOROMETHYL)-1H-INDOLE

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Company Name: Capot Chemical Co.,Ltd.
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Products Intro: Product Name:4-(Trifluoromethyl)indole
CAS:128562-95-8
Purity:98%(Min,GC) Package:100g;1kg;5kg,10kg,25kg,50kg
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Products Intro: Product Name:4-(TRIFLUOROMETHYL)-1H-INDOLE
CAS:128562-95-8
Purity:98% Package:25G;50G;100G;500G;1KG;10KG;50KG
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Products Intro: Product Name:4-(TRIFLUOROMETHYL)-1H-INDOLE
CAS:128562-95-8
Purity:99% Package:1g;1USD
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Products Intro: Product Name:4-(Trifluoromethyl)indole
CAS:128562-95-8
Purity:99% Package:1kg; 25kg; or larger package as required
Company Name: Guangzhou Yuheng Pharmaceutical Technology Co., Ltd
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Products Intro: Product Name:4-(trifluoromethyl)-1H-indole
CAS:128562-95-8
Purity:0.97 Package:1KG;25KG

4-(TRIFLUOROMETHYL)-1H-INDOLE manufacturers

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
EINECS:
Product Categories:
Mol File:128562-95-8.mol
4-(TRIFLUOROMETHYL)-1H-INDOLE Structure
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)
Fp 109.0±25.9℃
storage temp. under inert gas (nitrogen or Argon) at 2-8°C
pka15.59±0.30(Predicted)
form Solid
AppearanceBrown to black Liquid
CAS DataBase Reference128562-95-8
Safety Information
HS Code 2933998090
MSDS Information
4-(TRIFLUOROMETHYL)-1H-INDOLE Usage And Synthesis
Synthesis
EthenaMine, N,N-diMethyl-2-[2-nitro-6-(trifluoroMethyl)phenyl]-, (1E)-

905274-06-8

4-(TRIFLUOROMETHYL)-1H-INDOLE

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-INDOLE Preparation Products And Raw materials
Raw materialsEthenaMine, N,N-diMethyl-2-[2-nitro-6-(trifluoroMethyl)phenyl]-, (1E)--->2-Methyl-3-nitrobenzotrifluoride
Tag:4-(TRIFLUOROMETHYL)-1H-INDOLE(128562-95-8) Related Product Information
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