Skip to Content
Merck
All Photos(1)

Documents

559490

Sigma-Aldrich

3,4,5-Trifluoroaniline

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
F3C6H2NH2
CAS Number:
Molecular Weight:
147.10
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

61-64 °C (lit.)

SMILES string

Nc1cc(F)c(F)c(F)c1

InChI

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

InChI key

SZRDJHHKIJHJHQ-UHFFFAOYSA-N

General description

3,4,5-Trifluoroaniline can be prepared from pentafluoroacetanilide, via catalytic hydrodefluorination.

Application

3,4,5-Trifluoroaniline may be used to synthesize:
  • (E)-1-(2-nitrophenyl)-2-(3,4,5-trifluorophenyl)diazene
  • 2,5-dibromo-3,4,5-trifluoroaniline
  • 3,4,5-trifluoro-2,6-dibromoaniline
  • 3,4,5-trifluoro-2,6-diiodoaniline
  • (E)-1,2-bis(3,4,5-trifluorophenyl)diazene

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

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’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Customers Also Viewed

Polyfluorinated versus cationic multidentate halogen-bond donors: A direct comparison.
Walter SM, et al.
Journal of Fluorine Chemistry, 150, 14-20 (2013)
2-Aryl-2 H-benzotriazoles as Building Blocks for New Low-Bandgap Poly (arylene- ethynylene) s.
Wettach H, et al.
Macromolecules, 41(24), 9513-9515 (2008)
The ionic liquid [bmim] Br as an alternative medium for the catalytic cleavage of aromatic C-F and C-Cl bonds.
Prikhod'ko SA, et al.
Tetrahedron Letters, 51(17), 2265-2268 (2010)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service