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101-23-5

101-23-5 Structure

101-23-5 Structure
IdentificationBack Directory
[Name]

N-phenyl-3-(trifluoromethyl)aniline
[CAS]

101-23-5
[Synonyms]

NSC 50453
Etofenamate EP Impurity C
m-Trifluoromethyldiphenylamine
3-Trifluoromethyl diphenylamine
N-Phenyl-a,a,a-tri-fluorotoluidine
N-phenyl-3-(trifluoromethyl)aniline
Phenyl(m-trifluoromethylphenyl)amine
3-Trifluoromethyl-N-phenylbenzenamine
N-Phenyl-3-(trifluoromethyl)benzenamine
N-(3-Trifluoromethylphenyl)-phenylamine
N-PHENYL-3-(TRIFLUIOROMETHYL)BENZENAMINE
Benzenamine, N-phenyl-3-(trifluoromethyl)-
Etofenamate Impurity 3 (Etofenamate EP Impurity C)
N-phenyl-3-(trifluoromethyl)aniline ISO 9001:2015 REACH
[EINECS(EC#)]

202-926-2
[Molecular Formula]

C13H10F3N
[MOL File]

101-23-5.mol
[Molecular Weight]

237.22
Chemical PropertiesBack Directory
[Boiling point ]

108-110 °C(Press: 0.3 Torr)
[density ]

1?+-.0.06 g/cm3(Predicted)
[refractive index ]

1.5655 (589.3 nm 25℃)
[storage temp. ]

2-8°C(protect from light)
[solubility ]

Chloroform (Slightly), Methanol (Slightly)
[form ]

Oil
[pka]

-0.36±0.30(Predicted)
[color ]

Colourless
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319-H335
[Precautionary statements ]

P261-P264-P270-P271-P280-P301+P312+P330-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501
Raw materials And Preparation ProductsBack Directory
[Raw materials]

1H-Imidazole-1-sulfonic acid, phenyl ester-->Sulfamic acid, dimethyl-, phenyl ester-->3-(Trifluoromethyl)phenyl trifluoromethanesulfonate-->3-Trifluoromethylphenylboronic acid, pinacol ester-->3-Iodobenzotrifluoride-->3-Chlorobenzotrifluoride-->Phenyl sulfoxide-->3-(Trifluoromethyl)phenylboronic acid-->Phenylboronic acid-->Aniline
[Preparation Products]

[1,1'-Biphenyl]-2-amine, 5-(trifluoromethyl)--->Ftormetazine
Hazard InformationBack Directory
[Chemical Properties]

Liquid. Boiling point 140-146°C/2.04-2.72kPa.
[Uses]

N-Phenyl-3-(trifluoromethyl)aniline can be used as fungicides.
[Synthesis]

Aniline

62-53-3

3-(Trifluoromethyl)phenylboronic acid

1423-26-3

N-phenyl-3-(trifluoromethyl)aniline

101-23-5

To a stirred solution of deionized water (10 mL) containing aniline (1.0 mmol), 3-(trifluoromethyl)phenylboronic acid (1.0 mmol), and K2CO3 (2.0 mmol) was added an aqueous suspension of FePd nanowires (3.0 mol%, dissolved in 3 mL H2O) at room temperature. The reaction mixture was stirred continuously for 5 h at room temperature. The reaction process was monitored by thin layer chromatography (TLC). Upon completion of the reaction, 2 M HCl solution was added and the catalyst was separated using an external magnet. Subsequently, the catalyst was washed with ethyl acetate (EtOAc). The reaction mixture was extracted with ethyl acetate (2 × 20 mL), and the organic phases were combined, dried over anhydrous sodium sulfate and concentrated. Finally, the residue was purified by gel permeation chromatography to afford the target product N-phenyl-3-(trifluoromethyl)aniline.

[References]

[1] Tetrahedron Letters, 2014, vol. 55, # 17, p. 2813 - 2817
Spectrum DetailBack Directory
[Spectrum Detail]

N-phenyl-3-(trifluoromethyl)aniline(101-23-5)1HNMR
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