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5-BROMO-2-METHOXYBENZYL ALCOHOL

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5-BROMO-2-METHOXYBENZYL ALCOHOL Basic information

Product Name:
5-BROMO-2-METHOXYBENZYL ALCOHOL
Synonyms:
  • RARECHEM AL BD 0053
  • BenzeneMethanol, 5-broMo-2-Methoxy-
  • 5-BroMo-2-Methoxybenzyl alcohol, 97% 5GR
  • 5-Brom-2-methoxybenzyl alcohol
  • 5-Bromo-2-methoxybenzyl alcohol 98%
  • 5-BROMO-O-ANISYL ALCOHOL
  • 5-BROMO-2-METHOXYBENZYL ALCOHOL
  • (5-BROMO-2-METHOXY-PHENYL)-METHANOL
CAS:
80866-82-6
MF:
C8H9BrO2
MW:
217.06
EINECS:
279-586-7
Product Categories:
  • Benzhydrols, Benzyl & Special Alcohols
  • Alcohol
  • Alcohols
  • Anisoles, Alkyloxy Compounds & Phenylacetates
  • Bromine Compounds
  • C7 to C8
  • Oxygen Compounds
Mol File:
80866-82-6.mol
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5-BROMO-2-METHOXYBENZYL ALCOHOL Chemical Properties

Melting point:
68-71 °C (lit.)
Boiling point:
192.5°C (rough estimate)
Density 
1.4816 (rough estimate)
refractive index 
1.4930 (estimate)
storage temp. 
Sealed in dry,Room Temperature
form 
powder to crystal
color 
White to Light yellow
CAS DataBase Reference
80866-82-6(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xn,Xi
Risk Statements 
36/37/38-22
Safety Statements 
37/39-26-24/25
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29094990

MSDS

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5-BROMO-2-METHOXYBENZYL ALCOHOL Usage And Synthesis

Chemical Properties

white to light yellow crystal powder

Uses

5-Bromo-2-methoxybenzyl alcohol has been used in the synthesis of 5-bromo-2-methoxyphenylacetic acid.

Synthesis

612-16-8

80866-82-6

GENERAL METHODS: Lithium bromide monohydrate (0.2 mmol) and iodobenzene diacetate (0.2 mmol) were added to a solution of 2-methoxybenzenemethanol (0.2 mmol) in trifluoroethanol (1 mL) and the reaction was carried out at room temperature. The progress of the reaction was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the reaction was quenched by the addition of saturated aqueous sodium sulfite solution. The mixture was extracted with dichloromethane and the combined organic layers were washed with saturated brine and dried over anhydrous sodium sulfate. The organic phase was concentrated under reduced pressure and the residue was purified by silica gel column chromatography to afford the target product 5-bromo-2-methoxybenzyl alcohol.

References

[1] Synlett, 2018, vol. 29, # 17, p. 2275 - 2278
[2] Tetrahedron Letters, 2000, vol. 41, # 46, p. 8881 - 8885
[3] Synthetic Communications, 2007, vol. 37, # 9, p. 1571 - 1577

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