ChemicalBook--->CAS DataBase List--->106877-29-6

106877-29-6

106877-29-6 Structure

106877-29-6 Structure
IdentificationBack Directory
[Name]

5-METHYL-2-(TRIFLUOROMETHYL)ANILINE
[CAS]

106877-29-6
[Synonyms]

5-METHYL-2-(TRIFLUOROMETHYL)ANILINE
5-Methyl-2-trifluoromethyl-phenylamine
5-Methyl-2-(trifluoromethyl)aniline,98%
Benzenamine, 5-methyl-2-(trifluoromethyl)-
[Molecular Formula]

C8H8F3N
[MDL Number]

MFCD04972928
[MOL File]

106877-29-6.mol
[Molecular Weight]

175.15
Chemical PropertiesBack Directory
[Boiling point ]

207.2±35.0 °C(Predicted)
[density ]

1.237±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C, protect from light
[pka]

1.59±0.10(Predicted)
[Appearance]

Yellow to brown Liquid
[Water Solubility ]

Slightly soluble in water.
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Warning
[Hazard statements ]

H302-H312-H315-H319-H331-H335
[Precautionary statements ]

P261-P280-P304+P340-P305+P351+P338-P405-P501a
[Hazard Codes ]

Xn
[Risk Statements ]

20/21/22-36/37/38-22
[Safety Statements ]

26-36/37/39
[RIDADR ]

2810
[HazardClass ]

6.1
[HS Code ]

2921420090
Spectrum DetailBack Directory
[Spectrum Detail]

5-METHYL-2-(TRIFLUOROMETHYL)ANILINE(106877-29-6)1HNMR
5-METHYL-2-(TRIFLUOROMETHYL)ANILINE(106877-29-6)FT-IR
Hazard InformationBack Directory
[Synthesis]

4-Methyl-2-nitro-1-(trifluoroMethyl)benzene

154057-13-3

5-METHYL-2-(TRIFLUOROMETHYL)ANILINE

106877-29-6

Step 1: 4-methyl-2-nitro-1-trifluoromethylbenzene (1 g, 4.8 mmol) and 30 mL of methanol were added to a 100 mL reaction vial. Pd/C catalyst (0.2 g, 10% content) was then added. The reaction mixture was stirred under hydrogen atmosphere (1 atm, 25°C) for 4 hours. Upon completion of the reaction, the reaction solution was filtered to remove the catalyst and the filtrate was concentrated. The residue was purified by column chromatography (eluent: ethyl acetate/petroleum ether = 1:10) to afford 2-amino-4-methylbenzotrifluoride (0.68 g, 80% yield). Mass spectrometry analysis: [M+1]+ 176.2.

[References]

[1] Patent: EP3150592, 2017, A1. Location in patent: Paragraph 0133; 0134; 0135
[2] Bioorganic and Medicinal Chemistry Letters, 2015, vol. 25, # 17, p. 3738 - 3743
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