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ChemicalBook >  Product Catalog >  Organic Chemistry >  Alcohols,Phenols,Phenol alcohols >  1-(2-METHOXYPHENYL)ETHANOL

1-(2-METHOXYPHENYL)ETHANOL

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1-(2-METHOXYPHENYL)ETHANOL Basic information

Product Name:
1-(2-METHOXYPHENYL)ETHANOL
Synonyms:
  • 2-(2-METHOXYPHENYL)ETHANOL
  • 2-METHOXYPHENETHYL ALCOHOL
  • 2-METHOXYPHENYL METHYL CARBINOL
  • 1-(2-METHOXYPHENYL)ETHANOL
  • DL-2-METHOXY-ALPHA-METHYLBENZYL ALCOHOL
  • ALPHA-METHYL-2-METHOXYBENZYL ALCOHOL
  • 2-methoxy-benzeneethano
  • Phenethyl alcohol, o-methoxy-
CAS:
7417-18-7
MF:
C9H12O2
MW:
152.19
EINECS:
231-029-9
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohols
  • C9 to C30
  • Oxygen Compounds
Mol File:
7417-18-7.mol
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1-(2-METHOXYPHENYL)ETHANOL Chemical Properties

Melting point:
37 °C
Boiling point:
133-135 °C/10 mmHg (lit.)
Density 
1.076 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.54(lit.)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
clear liquid
pka
14.89±0.10(Predicted)
color 
Colorless to Light yellow
InChI
InChI=1S/C9H12O2/c1-11-9-5-3-2-4-8(9)6-7-10/h2-5,10H,6-7H2,1H3
InChIKey
XLDRDNQLEMMNNH-UHFFFAOYSA-N
SMILES
C1(CCO)=CC=CC=C1OC
LogP
1.557 (est)
CAS DataBase Reference
7417-18-7(CAS DataBase Reference)
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Safety Information

Safety Statements 
24/25
WGK Germany 
3
HS Code 
29094990

MSDS

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1-(2-METHOXYPHENYL)ETHANOL Usage And Synthesis

Uses

2-Methoxyphenethyl alcohol may be used in chemical synthesis.

Synthesis

7768-28-7

74-88-4

7417-18-7

Step A: To a stirred suspension of 2-(2-hydroxyethyl)phenol (5 g, 36.2 mmol) and cesium carbonate (Cs2CO3, 38.9 g, 108.7 mmol) in acetone (100 mL) was slowly added iodomethane (6.2 g, 43.4 mmol) under ice-bath conditions. The reaction mixture was stirred continuously at 0 °C for 50 min. Upon completion of the reaction, the mixture was filtered to remove insoluble salts and the filtrate was concentrated under reduced pressure by rotary evaporator. The concentrated crude product was subjected to liquid-liquid extraction with ethyl acetate (EtOAc) and water. The organic layer was separated and dried with anhydrous sodium sulfate (Na2SO4), and the dried organic layer was concentrated by filtration to give 2-(2-methoxyphenyl)ethanol (4.5 g, 29.6 mmol, 82% yield) as a yellow solid.

References

[1] Patent: WO2015/142903, 2015, A2. Location in patent: Page/Page column 96
[2] Patent: WO2015/140133, 2015, A1. Location in patent: Page/Page column 108
[3] Patent: WO2003/103653, 2003, A1. Location in patent: Page 184-185

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