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3,5-Difluorobenzonitrile

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3,5-Difluorobenzonitrile Basic information
Uses
Product Name:3,5-Difluorobenzonitrile
Synonyms:5-CYANO-1,3-DIFLUOROBENZENE;3,5-DIFLUOROBENZONITRILE;LABOTEST-BB LT00847812;3,5-Difluorobenzonitril;Benzonitrile, 3,5-difluoro- (9CI);3,5-Difluorobenzonitrile,99%;3,5-DIFLUOROBENZEONITRILE;3,5-Difluorobenzonitrile98%
CAS:64248-63-1
MF:C7H3F2N
MW:139.1
EINECS:264-752-3
Product Categories:Pyrazines;C6 to C7;Cyanides/Nitriles;Nitrogen Compounds;FINE Chemical & INTERMEDIATES;Aromatic Nitriles;Fluorobenzene;Fluorobenzonitrile Series;Fluorine series;Fluorobenzene Series;NITRILE
Mol File:64248-63-1.mol
3,5-Difluorobenzonitrile Structure
3,5-Difluorobenzonitrile Chemical Properties
Melting point 84-86 °C(lit.)
Boiling point 160 °C
density 1.2490 (estimate)
storage temp. Sealed in dry,Room Temperature
Water Solubility Insoluble in water
form powder to crystal
color White to Almost white
BRN 2082206
InChIInChI=1S/C7H3F2N/c8-6-1-5(4-10)2-7(9)3-6/h1-3H
InChIKeyCQXZSEXZQVKCHW-UHFFFAOYSA-N
SMILESC(#N)C1=CC(F)=CC(F)=C1
CAS DataBase Reference64248-63-1(CAS DataBase Reference)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 20/21/22-36/37/38
Safety Statements 26-36-36/37/39-36/37
RIDADR 3276
WGK Germany 3
Hazard Note Harmful/Irritant
HazardClass 6.1
PackingGroup III
HS Code 29269090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Dermal
Acute Tox. 4 Inhalation
Acute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
MSDS Information
ProviderLanguage
3,5-Difluorobenzonitrile English
ACROS English
SigmaAldrich English
ALFA English
3,5-Difluorobenzonitrile Usage And Synthesis
Uses3,5-Difluorobenzonitrile is an aromatic nitrile compound. Aromatic nitrile compounds have a wide range of applications, serving not only as important chemical intermediates but also as key components in certain dyes, pesticides, and pharmaceuticals. 3,5-Difluorobenzonitrile can be synthesized from arylboronic acid.
Chemical Propertieswhite crystals
UsesThe vibrational wavenumbers, geometry and various thermodynamic parameters were studied for 3,5-difluorobenzonitrile.
Synthesis Reference(s)Journal of Medicinal Chemistry, 30, p. 486, 1987 DOI: 10.1021/jm00386a008
General DescriptionThe vibrational wavenumbers, geometry and various thermodynamic parameters were studied for 3,5-difluorobenzonitrile.
Synthesis
1-Bromo-3,5-difluorobenzene

461-96-1

3,5-Difluorobenzonitrile

64248-63-1

General procedure for the synthesis of 3,5-difluorobenzonitrile from 3,5-difluorobromobenzene: iPrMgCl (2M in THF, 4.1 mL) and THF (5 mL) were added to a flask containing dry LiCl (0.35 g, 8.24 mmol) at 15 °C. After stirring for 15 min, a solution of 3,5-difluorobromobenzene (1.46 g, 8.03 mmol) in THF (1 mL) was slowly added to the reaction mixture and stirring was continued for 15 min. Subsequently, DMF (1.3 mL, 12 mmol) was added at 0 °C and the mixture was stirred for 2 hours. After completion of the reaction, aqueous NH3 (7 mL, 28-30%) and I2 (4.06 g, 16 mmol) were added to the mixture. After stirring at room temperature for 2 h, the reaction mixture was poured into saturated aqueous Na2SO3 solution and extracted with CHCl3 (3 x 30 mL). The organic layers were combined, dried with Na2SO4 and filtered. After removing the solvent under reduced pressure, the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate = 9:1, v/v) to afford pure 3,5-difluorobenzonitrile (0.73 g) in 71% yield. Most of the nitrile compounds involved in this study were commercially available and were identified by comparison with real samples.

References[1] Tetrahedron, 2013, vol. 69, # 5, p. 1462 - 1469
Tag:3,5-Difluorobenzonitrile(64248-63-1) Related Product Information
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