ChemicalBook--->CAS DataBase List--->106877-20-7

106877-20-7

106877-20-7 Structure

106877-20-7 Structure
IdentificationBack Directory
[Name]

3-Methoxy-4-(trifluoromethyl)phenylamine
[CAS]

106877-20-7
[Synonyms]

3-Methoxy-4-(trifluoromethyl)
3-Methoxy-4-(trifluoromethyl)phenylamine
3-Methoxy-4-(trifluoromethyl)benzenamine
Benzenamine, 3-methoxy-4-(trifluoromethyl)-
[Molecular Formula]

C8H8F3NO
[MDL Number]

MFCD11840978
[MOL File]

106877-20-7.mol
[Molecular Weight]

191.15
Chemical PropertiesBack Directory
[Melting point ]

49-50°
[storage temp. ]

-20°C, sealed storage, away from moisture
[Appearance]

Light yellow to yellow Solid
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[HazardClass ]

IRRITANT
[HS Code ]

2922190090
Spectrum DetailBack Directory
[Spectrum Detail]

3-Methoxy-4-(trifluoromethyl)phenylamine(106877-20-7)1HNMR
3-Methoxy-4-(trifluoromethyl)phenylamine(106877-20-7)19FNMR
Hazard InformationBack Directory
[Synthesis]

2-Methoxy-4-nitro-1-(trifluoromethyl)benzene

453560-74-2

3-Methoxy-4-(trifluoromethyl)phenylamine

106877-20-7

General procedure for the synthesis of 3-methoxy-4-(trifluoromethyl)aniline from 2-methoxy-4-nitro-1-(trifluoromethyl)benzene: Intermediate 444 (7.1 g, 28.9 mmol) was dissolved in methanol (100 mL) followed by addition of 5% Pd/C catalyst (0.7 g). The reaction mixture was hydrogenated under hydrogen atmosphere (50 Psi) for 48 hours at room temperature. Upon completion of the reaction, the catalyst was removed by filtration and the filtrate was concentrated under reduced pressure to give Intermediate 445 (7 g) as a white solid.

[References]

[1] Journal of Medicinal Chemistry, 2014, vol. 57, # 5, p. 1914 - 1931
[2] Patent: US2010/311760, 2010, A1. Location in patent: Page/Page column 42-43
[3] Patent: WO2017/32840, 2017, A1. Location in patent: Page/Page column 226
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