Skip to Content
Merck
All Photos(1)

Key Documents

264334

Sigma-Aldrich

3,4-Difluorobenzonitrile

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
F2C6H3CN
CAS Number:
Molecular Weight:
139.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

solid

mp

52-54 °C (lit.)

functional group

fluoro

SMILES string

Fc1ccc(cc1F)C#N

InChI

1S/C7H3F2N/c8-6-2-1-5(4-10)3-7(6)9/h1-3H

InChI key

BTBFCBQZFMQBNT-UHFFFAOYSA-N

Application

3,4-Difluorobenzonitrile has been used in the preparation of:
  • fluorophenoxy herbicides
  • fluorine substituted benzyl amides

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Flash Point(F)

156.2 °F - closed cup

Flash Point(C)

69 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Rajendra P Tangallapally et al.
Journal of medicinal chemistry, 48(26), 8261-8269 (2005-12-22)
In an ongoing effort to develop new and potent antituberculosis agents, a second-generation series of nitrofuranyl amides was synthesized on the basis of the lead compound 5-nitrofuran-2-carboxylic acid 3,4-dimethoxybenzylamide. The primary design consideration was to improve the solubility and consequently
Synthesis of 3, 4-difluorobenzonitrile and monofluorobenzonitriles by means of halogen-exchange fluorination.
Suzuki H and Kimura Y.
Journal of Fluorine Chemistry, 52(3), 341-351 (1991)

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