2-FLUORO-5-METHOXYBENZONITRILE CAS 127667-01-0
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 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 |
| InChI | 1S/C8H6FNO/c1-11-7-2-3-8(9)6(4-7)5-10/h2-4H,1H3 |
| InChIKey | VBZLRHYLNXWZIU-UHFFFAOYSA-N |
| SMILES | Fc1c(cc(cc1)OC)C#N |
| CAS DataBase Reference | 127667-01-0(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 Class | 6.1C - Combustible acute toxic Cat.3 toxic compounds or compounds which causing chronic effects |
| Hazard Classifications | Acute Tox. 3 Dermal Acute Tox. 3 Inhalation Acute Tox. 3 Oral Skin Irrit. 2 STOT SE 3 |
| 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 |
2-FLUORO-5-METHOXYBENZONITRILE Preparation Products And Raw materials
| Raw materials | Benzaldehyde, 2-fluoro-5-methoxy-, oxime-->3-CHLORO-4-FLUOROANISOLE-->2-FLUORO-5-METHOXYBENZALDEHYDE-->5-Bromo-2-fluorobenzonitrile-->Methanol-->4-Fluoroanisole-->Triethylamine-->Copper(I) Cyanide-->Trifluoroacetic anhydride-->Tetrahydrofuran |
| Preparation Products | 2-Fluoro-5-hydroxybenzenecarbonitrile-->2-FLUORO-5-HYDROXYBENZOIC ACID |
