ChemicalBook--->CAS DataBase List--->363-80-4

363-80-4

363-80-4 Structure

363-80-4 Structure
IdentificationMore
[Name]

2,3,5-TRIFLUOROANILINE
[CAS]

363-80-4
[Synonyms]

2,3,5-TRIFLUOROANILINE
2,3,5-Trifluoroaniline 98%
2,3,5-Trifluoroaniline98%
[Molecular Formula]

C6H4F3N
[MDL Number]

MFCD00083549
[Molecular Weight]

147.1
[MOL File]

363-80-4.mol
Chemical PropertiesBack Directory
[Boiling point ]

175℃
[density ]

1.409
[Fp ]

69℃
[refractive index ]

1.4895
[storage temp. ]

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

liquid
[pka]

1.18±0.10(Predicted)
[color ]

Clear, faint brown
[Specific Gravity]

1.390
[CAS DataBase Reference]

363-80-4(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[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 ]

UN2810
[Hazard Note ]

Irritant
[HazardClass ]

6.1
[HazardClass ]

IRRITANT
[HS Code ]

2921420090
Spectrum DetailBack Directory
[Spectrum Detail]

2,3,5-TRIFLUOROANILINE(363-80-4)1HNMR
2,3,5-TRIFLUOROANILINE(363-80-4)19FNMR
Well-known Reagent Company Product InformationBack Directory
[Alfa Aesar]

2,3,5-Trifluoroaniline, 97%(363-80-4)
Hazard InformationBack Directory
[Synthesis]

Aniline

62-53-3

2,3,5-TRIFLUOROANILINE

363-80-4

The general procedure for the synthesis of 2,3,5-trifluoroaniline from aniline was as follows: 9.3 g (0.1 mol) of aniline was dissolved in 50 mL of glacial acetic acid, cooled to 10 °C, and then 8.2 g (0.12 mol) of sodium nitrite was slowly added. Subsequently, a solution prepared from 33 g (0.3 mol) sodium borohydride dissolved in 50 mL of water was added slowly and dropwise at the same temperature. After completion of the reaction, the product was separated by filtration. The filtrate was extracted by adding 100 mL of ethyl acetate to the filtrate and this operation was repeated three times. The organic phases were combined and washed sequentially with 10 mL of aqueous sodium fluoroborate and 50 mL of pure water. Finally, the organic phase was evaporated to dryness to give 9 g of 2,3,5-trifluoroaniline.

[References]

[1] Patent: CN107522609, 2017, A. Location in patent: Paragraph 0015; 0018; 0019
[2] Patent: CN107673951, 2018, A. Location in patent: Paragraph 0013
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