Basic information Safety Supplier Related

2-Chloro-4-methoxy-1-methylbenzene

Basic information Safety Supplier Related

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
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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)
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Safety Information

Hazard Codes 
Xi,F
HazardClass 
IRRITANT, FLAMMABLE
HS Code 
2909309090
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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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