103713
2,3,4,5,6-Pentafluoroaniline
99%
Synonym(s):
Pentafluoroaniline
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Linear Formula:
C6F5NH2
CAS Number:
Molecular Weight:
183.08
Beilstein:
1819387
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
99%
form
solid
bp
153 °C (lit.)
mp
33-35 °C (lit.)
solubility
toluene: soluble
functional group
fluoro
SMILES string
Nc1c(F)c(F)c(F)c(F)c1F
InChI
1S/C6H2F5N/c7-1-2(8)4(10)6(12)5(11)3(1)9/h12H2
InChI key
NOXLGCOSAFGMDV-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
General description
2,3,4,5,6-Pentafluoroaniline forms metal-drug complexes, cis-Pt-(2,3,4,5,6-pentafluoroaniline)2-Br2 which has been tested against the promastigote forms of Leishmania donovani.
Application
2,3,4,5,6-Pentafluoroaniline may be used in the preparation of pentafluorophenylammonium triflate, an efficient catalyst for esterification and thioesterification. 2,3,4,5,6-Pentafluoroaniline was used in synthesis of various titanium complexes having two anionic [N, O–] bidentate salicylaldiminato ligands.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
163.4 °F
Flash Point(C)
73 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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.
Bis (salicylaldiminato) titanium complexes containing bulky imine substituents: Synthesis, characterization and ethene polymerization studies.
Parssinen A, et al.
European Journal of Inorganic Chemistry, 2005(11), 2100-2109 (2005)
Pentafluorophenylammonium triflate (PFPAT): an efficient, practical, and cost-effective catalyst for esterification, thioesterification, transesterification, and macrolactone formation.
Funatomi T, et al.
Green Chemistry, 8(12), 1022-1027 (2006)
C M Mesa-Valle et al.
The Journal of antimicrobial chemotherapy, 40(1), 47-57 (1997-07-01)
The action of 16 newly synthesized metal complexes having the general structure cis-Pt-(II)-Xn-Ln have been tested in vitro against the promastigote forms of Leishmania donovani. The metal complexes at 24 h and maximum dosages inhibited growth from 0%, e.g. in
Vasily A Ilichev et al.
Dalton transactions (Cambridge, England : 2003), 48(3), 1060-1066 (2019-01-03)
To obtain new efficient lanthanide-based NIR luminophores perfluorinated 2-mercaptobenzothiazole was used as a ligand. The ate-complexes [(Ln(mbtF)4)-(Na(DME)3)+] of Nd (1), Sm (2), Tb (3), Er (4), Yb (5) and [(Y(mbtF)4)-(Li(DME)3)+] (6) were synthesized in high yields by the reactions of
I M Rietjens et al.
Chemico-biological interactions, 77(3), 263-281 (1991-01-01)
Metabolism and bioactivation of fluoroanilines was studied both in vitro in microsomal systems and in vivo. 4-Fluoroaniline and pentafluoroaniline and their non-para fluorinated analogues were used as the model compounds. Special attention was focussed on bioactivation to reactive benzoquinoneimines. Cytochrome
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