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Sigma-Aldrich

2,6-Difluorobenzonitrile

97%

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About This Item

Linear Formula:
F2C6H3CN
CAS Number:
1897-52-5
Molecular Weight:
139.10
Beilstein:
2045292
EC Number:
217-589-7
MDL number:
MFCD00001778
UNSPSC Code:
12352100
PubChem Substance ID:
24851242
NACRES:
NA.22

Assay

97%

form

solid

refractive index

n20/D 1.4875 (lit.)

bp

197-198 °C

mp

25-28 °C (lit.)

density

1.246 g/mL at 25 °C (lit.)

SMILES string

Fc1cccc(F)c1C#N

InChI

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

InChI key

BNBRIFIJRKJGEI-UHFFFAOYSA-N

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Application

2,6-Difluorobenzonitrile was used in the synthesis of:
  • poly(cyanoaryl ethers) via silyl-method
  • 2-dimethylamino-6-fluorobenzamide
  • phenolphthalein-modified polyarylene ether nitrile copolymers

Pictograms

Exclamation mark
GHS07

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

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

194.0 °F - closed cup

Flash Point(C)

90 °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’.

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Xiaocan Liu et al.
Polymers, 11(9) (2019-08-31)
Porous materials with high specific surface area possess a broad application prospect in the treatment of wastewater. In this work, sulfonated poly(arylene ether nitrile) (SPEN) functionalized with a carboxylic acid group was successfully synthesized, which was subsequently transformed into SPEN
New polymer syntheses, 15 Syntheses of aromatic polyethers from difluorobenzonitriles and silylated diphenols.
Kricheldorf HR, et al.
Makromol. Chem., Rapid Commun., 8(11), 529-534 (1987)
Synthesis and laboratory evaluation of 1-(2,6-disubstituted benzoyl)-3-phenylureas, a new class of insecticides. II. Influence of the acyl moiety on insecticidal activity.
K Wellinga et al.
Journal of agricultural and food chemistry, 21(6), 993-998 (1973-11-01)
Synthesis and properties of phenolphthalein-based polyarylene ether nitrile copolymers.
Li C, et al.
Materials Letters, 60(1), 137-141 (2006)
Chenfeng He et al.
Journal of colloid and interface science, 466, 168-177 (2016-01-02)
The effect of annealing on the surface hydrophilicity of various representative classes of hydrocarbon-based proton exchange membranes (PEMs) is investigated. In all cases, a more hydrophilic membrane surface develops after annealing at elevated temperatures. The annealing time also had some
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