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3-Hydroxy-4-methoxybenzyl alcohol

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3-Hydroxy-4-methoxybenzyl alcohol Basic information

Product Name:
3-Hydroxy-4-methoxybenzyl alcohol
Synonyms:
  • 3-Hydroxy-4-Methoxybenzyl alcohol, 98%, 98%
  • 3-Hydroxy-4-methoxybenzyl alcohol 98%
  • RARECHEM AL BD 0068
  • 3-HYDROXY-4-METHOXYBENZYL ALCOHOL
  • ISOVANILLYL ALCOHOL
  • 4-Methoxy-3-hydroxy benzyl alcohol
  • 5-(Hydroxymethyl)-2-methoxyphenol
  • Benzenemethanol, 3-hydroxy-4-methoxy-
CAS:
4383-06-6
MF:
C8H10O3
MW:
154.16
EINECS:
224-489-7
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
Mol File:
4383-06-6.mol
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3-Hydroxy-4-methoxybenzyl alcohol Chemical Properties

Melting point:
135-137 °C (lit.)
Boiling point:
315.8±27.0 °C(Predicted)
Density 
1.226±0.06 g/cm3(Predicted)
storage temp. 
Inert atmosphere,Room Temperature
solubility 
soluble in Methanol
form 
powder to crystal
pka
9.75±0.10(Predicted)
color 
White to Almost white
BRN 
1867860
CAS DataBase Reference
4383-06-6(CAS DataBase Reference)
NIST Chemistry Reference
3-Hydroxy-4-methoxybenzyl alcohol(4383-06-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
22-24/25-36-26
WGK Germany 
3
HS Code 
29094990

MSDS

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3-Hydroxy-4-methoxybenzyl alcohol Usage And Synthesis

Chemical Properties

White crystalline

Uses

3-Hydroxy-4-methoxybenzyl alcohol was used in preparation of 2-hydroxymethyl-5-methoxy-2,5-cyclohexadiene-1,4-dione by oxidation with Fremy′s salt.

Synthesis

3-Hydroxy-4-methoxybenzyl alcohol is synthesised using isovanillin as raw material by chemical reaction. The specific synthesis steps are as follows:
In a round-bottom flask equipped with magnetic stirrer was added 15 sodium borohydride (0.2mmol; 0.01g) to the solution of 9 1 (0.2mmol; 0.03g) prepared in ethanol (1mL). The mixture was stirred at room temperature for 30min. The consumption of all starting material was detected by thin layer chromatography (TLC); the solvent was evaporated under reduced pressure. Subsequently, 10mL of saturated NaCl solution was added and then extracted with ethyl acetate (3×10mL). The organic phase was dried over anhydrous MgSO4, filtered and evaporated, providing 0.03g of colorless oil, 90% yield of 3-Hydroxy-4-methoxybenzyl alcohol.

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