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311081

Sigma-Aldrich

2,4,5-Trifluoroaniline

99%

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About This Item

Linear Formula:
F3C6H2NH2
CAS Number:
Molecular Weight:
147.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:

assay

99%

mp

59-63 °C (lit.)

SMILES string

Nc1cc(F)c(F)cc1F

InChI

1S/C6H4F3N/c7-3-1-5(9)6(10)2-4(3)8/h1-2H,10H2

InChI key

QMYVWJVVVMIBMM-UHFFFAOYSA-N

Application

2,4,5-Trifluoroaniline was used in the synthesis of 1,2,4-trifluoro-5-nitrobenzene by reacting with acetonitrile and aqueous acetonitrile.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

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Christopher B McPake et al.
ChemSusChem, 5(2), 312-319 (2011-12-16)
The generation and use of the highly potent oxidising agent HOF·MeCN in a controlled single continuous flow process is described. Oxidations of amines and azides to corresponding nitrated systems by using fluorine gas, water and acetonitrile by sequential gas-liquid/liquid-liquid continuous
Mohamad Shazwan Shah Jamil et al.
Dalton transactions (Cambridge, England : 2003), 48(25), 9317-9327 (2019-06-06)
A series of imidazolium salts precursors for N-heterocyclic carbenes (NHCs) featuring fluoroaryl substituents have been prepared along with their selenides and rhodium complexes. Tests of the catalytic activity of the [Rh(cod)Cl(NHC)] complexes in the transfer hydrogenation of acetophenone with iPrOH

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