All Photos(1)
Linear Formula:
F3C6H2NH2
CAS Number:
Molecular Weight:
147.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
≥97%
form
solid
bp
57 °C/22 mmHg (lit.)
mp
33-37 °C (lit.)
SMILES string
Nc1c(F)cc(F)cc1F
InChI
1S/C6H4F3N/c7-3-1-4(8)6(10)5(9)2-3/h1-2H,10H2
InChI key
BJSVKBGQDHUBHZ-UHFFFAOYSA-N
Application
2,4,6-Trifluoroaniline was used in the synthesis of:
- 3-nitro-2,4,6 -trifluoroacetanilide
- series of N′-phenyl-N-(1- phenyl cyclopentyl)-methyl ureas
- 4-substituted 2,6-difluoro N-aryl pyridinones
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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T S Purchase et al.
Bioorganic & medicinal chemistry, 5(4), 739-747 (1997-04-01)
Our continued interest in developing novel, potent acyl-CoA:cholesterol acyltransferase (ACAT) inhibitors, and our discovery of several active series of disubstituted urea ACAT inhibitors, have led us to investigate a series of trisubstituted ureas that are structural hybrids of our disubstituted
EPR spectroscopy of a diaza derivative of meta-xylylene.
Haider K, et al.
Tetrahedron Letters, 30(10), 1225-1228 (1989)
Shaun R Selness et al.
Bioorganic & medicinal chemistry letters, 21(13), 4059-4065 (2011-06-07)
A series of N-aryl pyridinone inhibitors of p38 mitogen activated protein (MAP) kinase were designed and prepared based on the screening hit SC-25028 (1) and structural comparisons to VX-745 (5). The focus of the investigation targeted the dependence of potency
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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