Phenol, 3-fluoro-5-methyl- (9CI)
Phenol, 3-fluoro-5-methyl- (9CI) Basic information
- Product Name:
- Phenol, 3-fluoro-5-methyl- (9CI)
- Synonyms:
-
- Phenol, 3-fluoro-5-methyl- (9CI)
- 3-Fluoro-5-hydroxytoluene, 5-Fluoro-m-cresol
- 3-Fluoro-5-methylphenol97%
- 3-Fluoro-5-methylphenol 97%
- 3-Fluoro-5-hydroxytoluene
- Phenol, 3-fluoro-5-methyl-
- CAS:
- 216976-31-7
- MF:
- C7H7FO
- MW:
- 126.13
- Product Categories:
-
- HALIDE
- ALCOHOL
- Mol File:
- 216976-31-7.mol
Phenol, 3-fluoro-5-methyl- (9CI) Chemical Properties
- Boiling point:
- 199.8±20.0 °C(Predicted)
- Density
- 1.164±0.06 g/cm3(Predicted)
- storage temp.
- 2-8°C
- pka
- 9.08±0.10(Predicted)
- Appearance
- Light yellow to yellow Liquid
- CAS DataBase Reference
- 216976-31-7
Safety Information
- Hazard Codes
- T
- HazardClass
- 8
- HS Code
- 2908990000
Phenol, 3-fluoro-5-methyl- (9CI) Usage And Synthesis
Synthesis
160911-11-5
216976-31-7
General procedure for the synthesis of 3-fluoro-5-methylphenol from 1-fluoro-3-methoxy-5-methylbenzene: (40b) Synthesis of 1-fluoro-5-methylphenol In Example (40a), 1-fluoro-3-methoxy-5-methylbenzene (0.92 g, 6.56 mmol) was dissolved in dichloromethane (20 mL), boron tribromide (1.0 M solution in dichloromethane, 8.53 mL, 8.53 mmol) was added, and the reaction was stirred for 10 hours at 0°C. After completion of the reaction, water (100 mL) was added to the reaction mixture and extracted with dichloromethane (100 mL). The organic layers were combined and dried over anhydrous sodium sulfate. After concentration under reduced pressure, the residue was purified by silica gel column chromatography (eluent: hexane/ethyl acetate, 1:1) to afford 3-fluoro-5-methylphenol (0.83 g, yield: 99%) as a yellow oil. 1H-NMR (CDCl3, 400 MHz) δ: 2.06 (3H, s), 4.97 (1H, s), 6.37 (1H, dt, J = 2.4, 10.2 Hz), 6.44 (1H, s), 6.48 (1H, d, J = 8.6 Hz).
References
[1] Patent: EP2138484, 2009, A1. Location in patent: Page/Page column 44
Phenol, 3-fluoro-5-methyl- (9CI)Supplier
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