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2-Fluoro-4-methylbenzonitrile

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CAS:85070-67-3
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CAS:85070-67-3
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2-Fluoro-4-methylbenzonitrile Basic information
Product Name:2-Fluoro-4-methylbenzonitrile
Synonyms:Benzonitrile, 2-fluoro-4-methyl- (9CI);2-Fluoro-4-methylbenzonitrile 98%;2-Fluoro-4-methylbenzonitrile98%;2-FLUORO-4-METHYLBENZONITRILE;2-Fluoro-4-methylbenzonitirile;2-Fluoro-4-methylben;4-Cyano-3-fluorotoluene;2-Fluoro-4-Methylbenzenecarbonitrile
CAS:85070-67-3
MF:C8H6FN
MW:135.14
EINECS:
Product Categories:Fluorine series;NITRILE;Fluorin-contained Benzonitrile series;Miscellaneous
Mol File:85070-67-3.mol
2-Fluoro-4-methylbenzonitrile Structure
2-Fluoro-4-methylbenzonitrile Chemical Properties
Melting point 52-53°C
Boiling point 219.6±20.0 °C(Predicted)
density 1.11±0.1 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form powder to crystal
color White to Orange to Green
Water Solubility Insoluble in water, soluble in chloroform, acetone and other organic solvents.
InChIInChI=1S/C8H6FN/c1-6-2-3-7(5-10)8(9)4-6/h2-4H,1H3
InChIKeyWCGNLBCJPBKXCN-UHFFFAOYSA-N
SMILESC(#N)C1=CC=C(C)C=C1F
CAS DataBase Reference85070-67-3(CAS DataBase Reference)
Safety Information
Hazard Codes T,Xi
Risk Statements 37/38-41-36/37/38-20/21/22
Safety Statements 26-39-36/37-9
RIDADR UN3439
Hazard Note Toxic
HazardClass 6.1
PackingGroup III
HS Code 29269090
MSDS Information
2-Fluoro-4-methylbenzonitrile Usage And Synthesis
Chemical PropertiesOff white crystalline
Uses2-Fluoro-4-methylbenzonitrile is used in the synthesis of fluorobenzamidrazone thrombin inhibitors.
Synthesis
4-Bromo-3-fluorotoluene

452-74-4

Copper(I) Cyanide

544-92-3

2-Fluoro-4-methylbenzonitrile

85070-67-3

Example 59 Preparation of 2-fluoro-4-methylbenzonitrile: 3-fluoro-4-bromotoluene (70 g, 370 mmol) and cuprous cyanide (50 g, 555 mmol) were dissolved in N,N-dimethylformamide (300 mL), heated to reflux and maintained for 24 hours. Upon completion of the reaction, the mixture was cooled to room temperature, followed by the addition of concentrated ammonia (300 mL) and ether (200 mL) with continuous stirring for 1 hour. The reaction mixture was extracted with ether (3 x 200 mL). All organic phases were combined and washed sequentially with saturated saline (3 x 200 mL) and dried over anhydrous sodium sulfate. Finally, the solvent was removed by distillation under reduced pressure to afford the light yellow solid product 2-fluoro-4-methylbenzonitrile (44 g, 88% yield). Mass spectrometry analysis showed a molecular ion peak (M + H)+ of 136.

References[1] Organic and Biomolecular Chemistry, 2004, vol. 2, # 9, p. 1339 - 1352
[2] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 20, p. 2925 - 2930
[3] Patent: WO2007/76092, 2007, A2. Location in patent: Page/Page column 74
[4] Journal of Organic Chemistry USSR (English Translation), 1992, vol. 28, # 7, p. 1135 - 1139
[5] Zhurnal Organicheskoi Khimii, 1992, vol. 28, # 7, p. 1439 - 1444
Tag:2-Fluoro-4-methylbenzonitrile(85070-67-3) Related Product Information
Tosylmethyl isocyanide Tetrafluoroterephthalonitrile 3'-(Trifluoromethyl)acetophenone 4-Cyanophenol 3-(Trifluoromethyl)benzoic acid 2-(Trifluoromethyl)benzoic acid 2-Fluoro-4-methylbenzoic acid Phenylmethylsulfonyl fluoride 3-(Trifluoromethyl)benzaldehyde 4-(Trifluoromethyl)benzaldehyde Benzotrifluoride Fluorine 2-Fluoro-4-(trifluoromethyl)benzonitrile 4-CYANO-2,3,5,6-TETRAFLUOROBENZOTRIFLUORIDE 4-(Aminomethyl)-2-fluorobenzonitrile 4-Cyano-3-fluorobenzoic acid Benzonitrile, 2,3-difluoro-4-methyl- (9CI) 3-FLUORO-4-METHYLBENZONITRILE,3-Fluoro-4-methylbenzonitrile 98%,3-Fluoro-4-methylbenzonitrile98%