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2-FLUORO-5-METHOXYBENZONITRILE

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Company Name: ShangHai DEMO Chemical Co.,Ltd  
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2-FLUORO-5-METHOXYBENZONITRILE manufacturers

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
EINECS:
Product Categories:Fluorine series;Nitrile;Anisoles, Alkyloxy Compounds & Phenylacetates;Fluorine Compounds;Nitriles;Aromatic Nitriles
Mol File:127667-01-0.mol
2-FLUORO-5-METHOXYBENZONITRILE Structure
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
InChI1S/C8H6FNO/c1-11-7-2-3-8(9)6(4-7)5-10/h2-4H,1H3
InChIKeyVBZLRHYLNXWZIU-UHFFFAOYSA-N
SMILESFc1c(cc(cc1)OC)C#N
CAS DataBase Reference127667-01-0(CAS DataBase Reference)
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
Storage Class6.1C - Combustible acute toxic Cat.3
toxic compounds or compounds which causing chronic effects
Hazard ClassificationsAcute Tox. 3 Dermal
Acute Tox. 3 Inhalation
Acute Tox. 3 Oral
Skin Irrit. 2
STOT SE 3
MSDS Information
2-FLUORO-5-METHOXYBENZONITRILE Usage And Synthesis
Synthesis
Benzaldehyde, 2-fluoro-5-methoxy-, oxime

796120-91-7

2-FLUORO-5-METHOXYBENZONITRILE

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
Tag:2-FLUORO-5-METHOXYBENZONITRILE(127667-01-0) Related Product Information
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