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3-Amino-4-iodobenzotrifluoride

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Products Intro: Product Name:3-Amino-4-iodobenzotrifluoride
CAS:105202-02-6
Purity:98%(Min,GC) Package:1G;1KG;100KG
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Products Intro: Product Name:3-Amino-4-iodobenzotrifluoride
CAS:105202-02-6
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Products Intro: Product Name:3-AMino-4-iodobenzotrifluoride
CAS:105202-02-6
Purity:97+% Package:1g;10g;100g;;1kg Remarks:Z-69419
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CAS:105202-02-6
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Products Intro: Product Name:2-Iodo-5-(trifluoromethyl)aniline
CAS:105202-02-6
Purity:99% Package:1kg; 25kg; or larger package as required

3-Amino-4-iodobenzotrifluoride manufacturers

3-Amino-4-iodobenzotrifluoride Basic information
Product Name:3-Amino-4-iodobenzotrifluoride
Synonyms:3-AMINO-4-IODOBENZOTRIFLUORIDE;3-Amino-4-iodobenzotrifluoride 98%;3-Amino-4-iodobenzotrifluoride98%;2-Iodo-5-(trifluoromethyl)aniline, 6-Iodo-alpha,alpha,alpha-trifluoro-m-toluidine;3-AMino-4-iodobenzotrifluoride[2-Iodo-5-(trifluoroMethyl)aniline];2-Iodo-5-(trifluoromethyl)aniline【3-Amino-4-iodobenzotrifluoride】;Benzenamine, 2-iodo-5-(trifluoromethyl)-
CAS:105202-02-6
MF:C7H5F3IN
MW:287.02
EINECS:
Product Categories:Fluorine series
Mol File:105202-02-6.mol
3-Amino-4-iodobenzotrifluoride Structure
3-Amino-4-iodobenzotrifluoride Chemical Properties
Boiling point 102-114°C
storage temp. under inert gas (nitrogen or Argon) at 2–8 °C
AppearanceYellow to brown Liquid
Safety Information
Hazard Codes Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36/37/39
Hazard Note Irritant
HS Code 2921490090
MSDS Information
3-Amino-4-iodobenzotrifluoride Usage And Synthesis
Chemical Propertiescolorless to light yellow liquid
Uses3-Amino-4-iodobenzotrifluoride is a useful intermediate for the preparation of trifluoromethylindoles by coupling-annulation of alkynes with iodo(trifluoromethyl)anilines.
Synthesis
4-IODO-3-NITROBENZOTRIFLUORIDE

400-97-5

3-Amino-4-iodobenzotrifluoride

105202-02-6

General procedure for the synthesis of 2-iodo-5-trifluoromethylaniline from 3-nitro-4-iodobenzotrifluoride: Iron powder (750 mg, 13.43 mmol) was added to a mixed HOAc-EtOH solution (10 mL, 1:5, v/v) of 3-nitro-4-iodobenzotrifluoride (850 mg, 2.68 mmol) at 23 °C. The reaction mixture was stirred at 23 °C for 3 h. The reaction was subsequently quenched with saturated NaHCO3 solution (20 mL) and diluted with EtOAc (50 mL). The organic and aqueous layers were separated and the organic layer was washed with deionized water (3 x 10 mL). The combined organic layers were dried over anhydrous Na2SO4 and concentrated under reduced pressure. The residue was purified by fast column chromatography (silica gel as stationary phase, eluent hexane:EtOAc, 10:1, v/v) to afford 2-iodo-5-trifluoromethylaniline (754 mg, 98% yield) as a yellow solid.1H NMR (400 MHz, CDCl3) δ = 7.76 (dd, J = 8.2,0.7Hz, 1H), 6.96 (d, J = 1.7 Hz, 1H), 6.72 (ddd, J=8.2,2.0,0.6 Hz, 1H), 4.32 (brs, 2H). Mass spectrum (ESI) m/z: 288.0 [M+H]+.

References[1] Patent: WO2016/29310, 2016, A1. Location in patent: Paragraph 00357-00359
[2] Patent: US5079245, 1992, A
[3] Angewandte Chemie - International Edition, 2011, vol. 50, # 32, p. 7354 - 7358
[4] Patent: US5998334, 1999, A
[5] Organic Letters, 2017, vol. 19, # 17, p. 4484 - 4487
3-Amino-4-iodobenzotrifluoride Preparation Products And Raw materials
Raw materials4-IODO-3-NITROBENZOTRIFLUORIDE-->Acetic acid-->Iron-->Ethanol
Tag:3-Amino-4-iodobenzotrifluoride(105202-02-6) Related Product Information
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