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311081

Sigma-Aldrich

2,4,5-Trifluoroaniline

99%

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About This Item

Linear Formula:
F3C6H2NH2
CAS Number:
367-34-0
Molecular Weight:
147.10
EC Number:
206-692-2
MDL number:
MFCD00007649
UNSPSC Code:
12352100
PubChem Substance ID:
24858836

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
GHS07

Signal Word

Warning

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

311081-BULK:
311081-1G:
311081-VAR:
311081-5G:

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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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