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2,5-DIMETHOXYBENZYL ALCOHOL

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2,5-DIMETHOXYBENZYL ALCOHOL Basic information

Product Name:
2,5-DIMETHOXYBENZYL ALCOHOL
Synonyms:
  • RARECHEM AL BD 0533
  • 2,5-DIMETHOXYBENZYL ALCOHOL
  • AURORA KA-7072
  • (2,5-Dimethoxyphenyl)methanol
  • Benzenemethanol, 2,5-dimethoxy-
  • 2,5-DIMETHOXYBENZYL ALCOHOL 99%
  • 2,5-Dimethoxy-1-(hydroxymethyl)benzene
  • 2,5-Dimethoxybenzenemethanol
CAS:
33524-31-1
MF:
C9H12O3
MW:
168.19
EINECS:
251-562-0
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohols
  • C9 to C30
  • Oxygen Compounds
Mol File:
33524-31-1.mol
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2,5-DIMETHOXYBENZYL ALCOHOL Chemical Properties

Melting point:
45-48 °C
Boiling point:
122-125 °C1 mm Hg(lit.)
Density 
1.173 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.547(lit.)
Flash point:
>230 °F
storage temp. 
2-8°C
solubility 
Chloroform, Methanol
form 
Viscous Liquid
pka
14.16±0.10(Predicted)
color 
Clear colorless to light yellow
BRN 
1947607
LogP
1.019 (est)
CAS DataBase Reference
33524-31-1(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
23-24/25-36/37-26
WGK Germany 
3
HS Code 
29094980

MSDS

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2,5-DIMETHOXYBENZYL ALCOHOL Usage And Synthesis

Chemical Properties

clear colorless to light yellow viscous liquid

Uses

2,5-Dimethoxybenzyl Alcohol can be used as a self-indicating standard for the determination of organolithium reagents

Uses

2,5-Dimethoxybenzyl alcohol was used as starting reagent in the synthesis of [(S)S]-3,6-dimethoxy-2-(p-tolylsulfinyl)-benzaldehyde. It was used in the synthesis of daunornycinone. It was also used in the preparation of pillar[n]arenes (n = 5 or 6) via cyclooligomerization reaction with an appropriate Lewis acid catalyst.

Synthesis Reference(s)

Tetrahedron Letters, 35, p. 6207, 1994 DOI: 10.1016/S0040-4039(00)73392-2

Synthesis

93-02-7

33524-31-1

General procedure for the synthesis of p-dimethoxybenzyl alcohol from 2,5-dimethoxybenzaldehyde: A solution of 2,5-dimethoxybenzaldehyde (3.32 g, 20 mmol) in THF (20 mL) was slowly added to a suspension of LiAlH4 (748 mg, 22 mmol) in THF (20 mL) at 0 °C. The reaction mixture was stirred at 0 °C for 30 min. Subsequently, the reaction was carefully quenched with saturated Na2SO4 solution (10 mL) at 0 °C and the resulting suspension was stirred for 3 hours. The reaction mixture was filtered through a silica gel pad and the filtrate was dried with Na2SO4. After evaporation of the solvent under reduced pressure, the residue was purified by column chromatography (petroleum ether-EtOAc, 1:1) to afford p-dimethoxybenzenemethanol as a colorless, thick liquid (3.06 g, 91%). rf = 0.4 (petroleum ether-EtOAc, 1:1).

References

[1] Journal of Organic Chemistry, 2007, vol. 72, # 24, p. 9190 - 9194
[2] Organic and Biomolecular Chemistry, 2010, vol. 8, # 17, p. 3965 - 3974
[3] Tetrahedron Letters, 2011, vol. 52, # 9, p. 983 - 986
[4] European Journal of Organic Chemistry, 2011, # 27, p. 5331 - 5335
[5] Green Chemistry, 2017, vol. 19, # 14, p. 3296 - 3301

2,5-DIMETHOXYBENZYL ALCOHOL Preparation Products And Raw materials

Preparation Products

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