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Key Documents

196835

Sigma-Aldrich

2,4,6-Trifluoroaniline

≥97%

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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:
NACRES:
NA.22

Assay

≥97%

form

solid

bp

57 °C/22 mmHg (lit.)

mp

33-37 °C (lit.)

functional group

fluoro

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 Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Flam. Sol. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
EPR spectroscopy of a diaza derivative of meta-xylylene.
Haider K, et al.
Tetrahedron Letters, 30(10), 1225-1228 (1989)
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

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