Basic information Safety Supplier Related

METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE

Basic information Safety Supplier Related

METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE Basic information

Product Name:
METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE
Synonyms:
  • METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE
  • SALOR-INT L446718-1EA
  • 5-bromo-2-hydroxy-4-methoxyBenzoic acid methyl ester
  • Benzoic acid, 5-bromo-2-hydroxy-4-methoxy-, methyl ester
CAS:
39503-52-1
MF:
C9H9BrO4
MW:
261.07
Mol File:
39503-52-1.mol
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METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE Chemical Properties

Melting point:
143 °C
Boiling point:
328.9±37.0 °C(Predicted)
Density 
1.573±0.06 g/cm3(Predicted)
storage temp. 
Sealed in dry,Room Temperature
pka
8.83±0.23(Predicted)
Appearance
White to off-white Solid
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METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATE Usage And Synthesis

Synthesis

98437-41-3

18107-18-1

39503-52-1

A) General procedure for synthesizing methyl 5-bromo-2-hydroxy-4-methoxybenzoate: to a solution of 5-bromo-2-hydroxy-4-methoxybenzoic acid (2.00 g) in methanol (10.0 mL) was slowly added a solution of 0.6 M (diazomethyl)trimethylsilane in hexanes (14.8 mL) under cooling conditions in an ice bath. The reaction mixture was stirred at room temperature for 3 hours. Upon completion of the reaction, acetic acid (0.12 mL) was added to quench the reaction, followed by evaporation of the solvent under reduced pressure. The resulting crude product was purified by silica gel column chromatography (eluent: ethyl acetate/hexane) to afford the target compound methyl 5-bromo-2-hydroxy-4-methoxybenzoate (2.08 g). The product was characterized by 1H NMR (300 MHz, CDCl3) with chemical shifts of δ3.91 (3H, s), 3.93 (3H, s), 6.49 (1H, s), 7.99 (1H, s), 10.93 (1H, s).

References

[1] Patent: WO2015/163485, 2015, A1. Location in patent: Paragraph 0342

METHYL 5-BROMO-2-HYDROXY-4-METHOXYBENZOATESupplier

Bide Pharmatech Ltd.
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Amadis Chemical Company Limited
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