ChemicalBook--->CAS DataBase List--->86225-73-2

86225-73-2

86225-73-2 Structure

86225-73-2 Structure
IdentificationBack Directory
[Name]

3-CHLORO-2,6-DIFLUOROBENZONITRILE
[CAS]

86225-73-2
[Synonyms]

3-CHLORO-2,6-DIFLUOROBENZONITRILE
Benzonitrile, 3-chloro-2,6-difluoro-
[Molecular Formula]

C7H2ClF2N
[MDL Number]

MFCD06660172
[MOL File]

86225-73-2.mol
[Molecular Weight]

173.55
Chemical PropertiesBack Directory
[refractive index ]

1.5125
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

Colorless to light yellow Liquid
[Water Solubility ]

Not miscible or difficult to mix with water.
[CAS DataBase Reference]

86225-73-2
Safety DataBack Directory
[Symbol(GHS) ]

Skull and Crossbones (GHS06)
GHS06
[Signal word ]

Danger
[Hazard statements ]

H302-H311-H315-H319-H332
[Precautionary statements ]

P280h-P305+P351+P338-P309-P310
[HazardClass ]

6.1
[HS Code ]

2926907090
Hazard InformationBack Directory
[Uses]

3-Chloro-2,6-difluorobenzonitrile is used as a pharmaceutical intermediate.
[Synthesis]

Benzonitrile, 2,3,6-trichloro-

4681-11-2

3-CHLORO-2,6-DIFLUOROBENZONITRILE

86225-73-2

(2) Fluorination step: In 800 g of dimethyl sulfoxide (DMSO), 206.5 g of 2,3,6-trichlorobenzonitrile was dissolved, followed by the addition of 145.3 g of potassium fluoride (KF) to the solution. The reaction mixture was heated to 170 °C with continuous stirring and maintained for 1.5 hours. After completion of the reaction, the mixture was poured into water and extracted with dichloromethane (DCM). After removing the solvent by distillation, the reaction mixture was further distilled and the fraction with a boiling point of 95 °C/11 mmHg was collected to give 166.6 g of 3-chloro-2,6-difluorobenzonitrile in 96.0% yield.

[References]

[1] Patent: US4406841, 1983, A
[2] Patent: US4406841, 1983, A
Spectrum DetailBack Directory
[Spectrum Detail]

3-CHLORO-2,6-DIFLUOROBENZONITRILE(86225-73-2)1HNMR
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