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2-CHLORO-4-METHOXYPHENOL

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2-CHLORO-4-METHOXYPHENOL Basic information

Product Name:
2-CHLORO-4-METHOXYPHENOL
Synonyms:
  • 3-CHLORO-4-HYDROXYANISOLE
  • 2-CHLORO-4-METHOXYPHENOL
  • 2-Chlorohydroquinonemonomethylether
  • 2-Chloro-4-methoxyphenol,97%
  • 2-chloro-4-methoxylphenol
  • 2-Chloro-4-Methoxyphenol, 97% 5GR
  • 3-Chloro-4-hydroxyanisole, 2-Chloro-p-guaiacol
  • 2-Chloro-4-methoxyphenol >
CAS:
18113-03-6
MF:
C7H7ClO2
MW:
158.58
EINECS:
242-007-3
Product Categories:
  • Aromatic Hydrocarbons (substituted) & Derivatives
  • Phenol&Thiophenol&Mercaptan
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Chlorine Compounds
  • Phenols
  • Organic Building Blocks
  • Oxygen Compounds
Mol File:
18113-03-6.mol
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2-CHLORO-4-METHOXYPHENOL Chemical Properties

Melting point:
41-44 °C(lit.)
Boiling point:
241°C (rough estimate)
Density 
1.153 g/mL at 25 °C(lit.)
Flash point:
185 °F
storage temp. 
Sealed in dry,2-8°C
form 
Crystalline Low Melting Solid
pka
8.98±0.18(Predicted)
Specific Gravity
1.153
color 
White to light yellow
BRN 
1936412
CAS DataBase Reference
18113-03-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29071990

MSDS

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2-CHLORO-4-METHOXYPHENOL Usage And Synthesis

Chemical Properties

WHITE TO LIGHT YELLOW CRYST. LOW MELTING SOLID

Synthesis

935-50-2

18113-03-6

General procedure for the synthesis of 2-chloro-4-methoxyphenol from 4,4-dimethoxycyclohexa-2,5-dien-1-one: 4,4-dimethoxycyclohexa-2,5-dien-1-one (1.0 mmol) was added to the reaction vessel, followed by the addition of a solution of 1,4-dioxane in 4N HCl (0.5 mL, 2 mmol) dropwise. The yellow color of the reaction mixture faded rapidly. After completion of the reaction, the solvent was removed by vacuum evaporation. The residue was diluted with ethyl acetate (10 mL) and washed with saturated aqueous NaHCO3 solution (5 mL). The organic layer was dried with anhydrous Na2SO4, filtered and concentrated to give 2-chloro-4-methoxyphenol in 95% yield. If necessary, it can be purified by column chromatography using ethyl acetate/hexane gradient elution.

References

[1] Organic and Biomolecular Chemistry, 2014, vol. 12, # 18, p. 2854 - 2858
[2] Tetrahedron Letters, 2016, vol. 57, # 1, p. 15 - 19

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