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2-FLUORO-5-METHOXYBENZONITRILE

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2-FLUORO-5-METHOXYBENZONITRILE Basic information

Product Name:
2-FLUORO-5-METHOXYBENZONITRILE
Synonyms:
  • 2-FLUORO-5-METHOXYBENZONITRILE
  • BUTTPARK 80\01-21
  • Fluoromethoxybenzonitrile2
  • 2-Fluoro-5-methyloxybenzonitrile
  • 2-Fluoro-5-methoxybenzonitrile98%
  • 6-Fluoro-m-anisonitrile
  • 3-Cyano-4-fluoroanisole
  • Benzonitrile, 2-fluoro-5-methoxy-
CAS:
127667-01-0
MF:
C8H6FNO
MW:
151.14
Product Categories:
  • Fluorine series
  • Nitrile
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Fluorine Compounds
  • Nitriles
  • Aromatic Nitriles
Mol File:
127667-01-0.mol
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2-FLUORO-5-METHOXYBENZONITRILE Chemical Properties

Melting point:
77-80°C
Boiling point:
232.7±25.0 °C(Predicted)
Density 
1.18±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
color 
White to Almost white
CAS DataBase Reference
127667-01-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
T
Risk Statements 
20/21/22-36/37/38-36/38
Safety Statements 
26-36/37/39-45-36/37
RIDADR 
3439
WGK Germany 
3
Hazard Note 
Toxic
HazardClass 
6.1
PackingGroup 
III
HS Code 
29269090
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2-FLUORO-5-METHOXYBENZONITRILE Usage And Synthesis

Synthesis

796120-91-7

127667-01-0

The general procedure for the synthesis of 2-fluoro-5-methoxybenzonitrile from the compound (CAS: 796120-91-7) was as follows: 15 g of 2-fluoro-5-methoxybenzaldehyde oxime was dissolved in 150 mL of tetrahydrofuran, followed by the addition of 40 g of trifluoroacetic anhydride. 20 mL of triethylamine was slowly added under stirring. Upon completion of the reaction, the reaction mixture was concentrated to remove the solvent. Water was added to the concentrate and extracted with ethyl acetate. The organic phase was separated, dried with anhydrous sodium sulfate, and then concentrated to obtain the crude product. The crude product was purified by silica gel column chromatography to give 11 g of 2-fluoro-5-methoxybenzonitrile.

References

[1] Patent: CN107778264, 2018, A. Location in patent: Paragraph 0029; 0030
[2] Patent: CN107698535, 2018, A. Location in patent: Paragraph 0029; 0030
[3] Patent: CN108129415, 2018, A. Location in patent: Paragraph 0029-0030

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