Skip to Content
Merck
All Photos(1)

Key Documents

196711

Sigma-Aldrich

2,3,4,5,6-Pentafluorobenzonitrile

99%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
C6F5CN
CAS Number:
Molecular Weight:
193.07
Beilstein:
1913453
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.442 (lit.)

bp

162-164 °C (lit.)

density

1.532 g/mL at 25 °C (lit.)

SMILES string

Fc1c(F)c(F)c(C#N)c(F)c1F

InChI

1S/C7F5N/c8-3-2(1-13)4(9)6(11)7(12)5(3)10

InChI key

YXWJGZQOGXGSSC-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

2,3,4,5,6-Pentafluorobenzonitrile was used in the synthesis of novel fluorinated poly(ether nitrile)s. It was also used in the synthesis of pentafluorophenyl analogs of noradrenaline, adrenaline and N-methyladrenaline.

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

84.2 °F - closed cup

Flash Point(C)

29 °C - closed cup

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

Highly fluorinated analogues of pharmacologically active compounds.
Chapman NB, et al.
J. Chem. Soc. Sect. C, 293-296 (1967)
Synthesis of novel fluorine-containing poly (aryl ether nitrile) s derived from 2, 3, 4, 5, 6-pentafluorobenzonitrile.
Kimura K, et al.
Polymer Journal, 33(3), 290-296 (2001)
Justin D Smith et al.
Nature communications, 10(1), 1837-1837 (2019-04-25)
Photocatalytic polymers offer an alternative to prevailing organometallics and nanomaterials, and they may benefit from polymer-mediated catalytic and material enhancements. MPC-1, a polymer photoredox catalyst reported herein, exhibits enhanced catalytic activity arising from charge transfer states (CTSs) between its two

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