311081
2,4,5-Trifluoroaniline
99%
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
About This Item
Linear Formula:
F3C6H2NH2
CAS Number:
Molecular Weight:
147.10
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
206-692-2
MDL number:
Assay:
99%
Quality Level
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.
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
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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