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3-METHOXY-5-METHYLPHENOL

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3-METHOXY-5-METHYLPHENOL Basic information

Product Name:
3-METHOXY-5-METHYLPHENOL
Synonyms:
  • 3-methoxy-5-methyl-pheno
  • 3-HYDROXY-5-METHOXYTOLUENE
  • 3-METHOXY-5-METHYLPHENOL
  • 5-METHOXY-M-CRESOL
  • ORCINOL MONOMETHYL ETHER
  • ORCINYL TER
  • TIMTEC-BB SBB008618
  • Methoxymethylphenol
CAS:
3209-13-0
MF:
C8H10O2
MW:
138.16
EINECS:
221-716-1
Product Categories:
  • Aromatics Compounds
  • Aromatics
  • Miscellaneous Reagents
Mol File:
3209-13-0.mol
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3-METHOXY-5-METHYLPHENOL Chemical Properties

Melting point:
59-63 °C (lit.)
Boiling point:
259 °C(Press: 755 Torr)
Density 
1.1106 g/cm3(Temp: 15 °C)
solubility 
Very slightly soluble in water, soluble in alcohol and oils
pka
9.70±0.10(Predicted)
form 
powder to crystal
color 
White to Almost white
Specific Gravity
1.11
Odor
at 10.00 % in dipropylene glycol. oakmoss fruity iodine woody hay
Odor Type
mossy
LogP
2.385 (est)
CAS DataBase Reference
3209-13-0(CAS DataBase Reference)
EPA Substance Registry System
Phenol, 3-methoxy-5-methyl- (3209-13-0)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36/37/39-37/39-37
WGK Germany 
2
TSCA 
Yes
HS Code 
29095090
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3-METHOXY-5-METHYLPHENOL Usage And Synthesis

Chemical Properties

Crystalline powder

Uses

3-Methoxy-5-methylphenol (cas# 3209-13-0) is a compound useful in organic synthesis.

Definition

ChEBI: 3-Methoxy-5-methylphenol is a member of phenols and a member of methoxybenzenes.

Synthesis Reference(s)

Organic Syntheses, Coll. Vol. 6, p. 859, 1988
The Journal of Organic Chemistry, 49, p. 1672, 1984 DOI: 10.1021/jo00183a043
Tetrahedron Letters, 11, p. 1327, 1970

Synthesis

A solution of anhydrous orcinol (12.4 g,0.1 mole) in dry acetone (100 ml)is refluxed for 4 hr with dimethyl sulphate (10.63 ml,14.2 g,0.112 mole) and ignited potassium carbonate (20 g) under anhydrous conditions. The mixture is filtered in hot, and the inorganic salts are washed with hot acetone(25 ml). The combined acetone solution is distilled. The oily product is purified by column chromatography over silica gel using chloroform as aneluant. Orcinol monomethyl ether is obtained as oil. Yield 4.2 g (30.4%).

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