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393-15-7

393-15-7 Structure

393-15-7 Structure
IdentificationMore
[Name]

5-AMINO-2-METHOXYBENZOTRIFLUORIDE
[CAS]

393-15-7
[Synonyms]

3-AMINO-6-METHOXYBENZOTRIFLUORIDE
3-TRIFLUOROMETHYL-P-ANISIDINE
4-METHOXY-3-(TRIFLUOROMETHYL)ANILINE
5-AMINO-2-METHOXYBENZOTRIFLUORIDE
TIMTEC-BB SBB002596
5-amino-2-methoxybenzotrifluoride,97%
3-Amino-6-methoxybenzotriflyoride
3-Amino-6-methoxybenzotrifloride
5-AMINO-2-METHOXYBENZOTRIFLUORIDE, 98+%
4-Methoxy-3-(trifluoromethyl)aniline, 98+%
[EINECS(EC#)]

670-719-8
[Molecular Formula]

C8H8F3NO
[MDL Number]

MFCD00043460
[Molecular Weight]

191.15
[MOL File]

393-15-7.mol
Chemical PropertiesBack Directory
[Melting point ]

28 °C
[Boiling point ]

112 °C
[density ]

1.280±0.06 g/cm3(Predicted)
[Fp ]

112°C/18mm
[storage temp. ]

Keep in dark place,Inert atmosphere,Room temperature
[form ]

solid
[pka]

3.98±0.10(Predicted)
[Appearance]

Yellow to brown Solid
[BRN ]

2723972
[InChI]

InChI=1S/C8H8F3NO/c1-13-7-3-2-5(12)4-6(7)8(9,10)11/h2-4H,12H2,1H3
[InChIKey]

CQJCPOVTPNWVBW-UHFFFAOYSA-N
[SMILES]

C1(N)=CC=C(OC)C(C(F)(F)F)=C1
[CAS DataBase Reference]

393-15-7(CAS DataBase Reference)
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

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

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

Xi,T
[Risk Statements ]

R20/21/22:Harmful by inhalation, in contact with skin and if swallowed .
R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
[RIDADR ]

UN2811
[Hazard Note ]

Irritant
[HazardClass ]

6.1
[HazardClass ]

TOXIC
[HS Code ]

2922290090
Hazard InformationBack Directory
[Uses]

4-Methoxy-3-(trifluoromethyl)aniline is a fluorinated aniline derivative used as a pharmaceutical intermediate for the synthesis of antibacterial and antiparasitic quinoxaline-2,3-diamine derivatives.
[Synthesis]

2-METHOXY-5-NITROBENZOTRIFLUORIDE

654-76-2

4-Methoxy-3-(trifluoromethyl)aniline

393-15-7

The general procedure for the synthesis of 4-methoxy-3-trifluoromethylaniline using 2-methoxy-5-nitrobenzotrifluoride as starting material was as follows: 2-methoxy-5-nitrobenzotrifluoride (5.08 g, 23.0 mmol) was dissolved in methanol (200 mL), and 10% Pd-C catalyst (50% water, 250 mg) was added. The reaction mixture was stirred continuously for 3.5 h at room temperature and under atmospheric pressure hydrogen atmosphere. Upon completion of the reaction, the catalyst was removed by diatomaceous earth filtration and the filtrate was concentrated to dryness under reduced pressure to afford 4-methoxy-3-(trifluoromethyl)aniline (4.67 g, 100% yield). Results of mass spectrometry analysis: m/z = 192 ([M+H]+).

[References]

[1] Patent: EP1403255, 2004, A1. Location in patent: Page 121
[2] Patent: US2005/209260, 2005, A1. Location in patent: Page/Page column 143-144
[3] Patent: US2007/49609, 2007, A1. Location in patent: Page/Page column 122
[4] Synthesis, 2006, # 19, p. 3316 - 3340
[5] Patent: FR745293, 1932,
Spectrum DetailBack Directory
[Spectrum Detail]

4-Methoxy-3-(trifluoromethyl)aniline(393-15-7)1HNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

4-Methoxy-3-(trifluoromethyl)aniline, 98+%(393-15-7)
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