2-Chloro-4-methoxy-1-methylbenzene
2-Chloro-4-methoxy-1-methylbenzene Basic information
- Product Name:
- 2-Chloro-4-methoxy-1-methylbenzene
- Synonyms:
-
- BENZENE, 2-CHLORO-4-METHOXY-1-METHYL
- 3-CHLORO-4-METHYLANISOLE
- 2-Chloro-4-Methoxytoluene
- 2-CHLORO-4-METHOXY-1-METHYLBENZENE
- 2-Chloro-4-Methoxy-1-MethylBenzene97%
- 3-CHLORO-4-METHYLANISOLE / 2-CHLORO-4-METHOXYTOLUENE
- CAS:
- 54788-38-4
- MF:
- C8H9ClO
- MW:
- 156.61
- Product Categories:
-
- Anisole
- Anisoles, Alkyloxy Compounds & Phenylacetates
- Chlorine Compounds
- Mol File:
- 54788-38-4.mol
2-Chloro-4-methoxy-1-methylbenzene Chemical Properties
- Boiling point:
- 76°C/2mm
- Density
- 1.105±0.06 g/cm3(Predicted)
- Flash point:
- 76°C/2mm
- refractive index
- 1.5340
- storage temp.
- Sealed in dry,Room Temperature
- form
- clear liquid
- color
- Colorless to Light yellow
- CAS DataBase Reference
- 54788-38-4(CAS DataBase Reference)
Safety Information
- Hazard Codes
- Xi,F
- HazardClass
- IRRITANT, FLAMMABLE
- HS Code
- 2909309090
2-Chloro-4-methoxy-1-methylbenzene Usage And Synthesis
Chemical Properties
Colorless liquid
Synthesis
615-62-3
74-88-4
54788-38-4
3-Chloro-4-methylphenol (15 g, 0.11 mol), iodomethane (9.8 mL, 0.16 mol) and potassium carbonate (22 g, 0.16 mol) were mixed in DMF (200 mL). The reaction mixture was heated to 50 °C with continuous stirring for 2 hours. After completion of the reaction, it was cooled to room temperature and the reaction was quenched with 1N HCl aqueous solution. Subsequently, the aqueous phase was extracted with ether (Et2O), the organic phase was washed with brine, dried with anhydrous magnesium sulfate (MgSO4) and filtered. Finally, the solvent was removed by distillation under reduced pressure to give 16.4 g (100% yield) of 3-chloro-4-methylanisole.
References
[1] Patent: US2009/111800, 2009, A1. Location in patent: Page/Page column 27
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2-Chloro-4-methoxy-1-methylbenzene(54788-38-4)Related Product Information
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- Ethacrynic acid
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- 1-CHLORO-4-METHOXY-2-METHYLBENZENE