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2-Benzyloxy-5-bromo-benzoic acid

CAS No.
62176-31-2
Chemical Name:
2-Benzyloxy-5-bromo-benzoic acid
Synonyms
Albb-008969;5-bromo-2-(phenylmethoxy)benzoic acid;Benzoic acid, 5-bromo-2-(phenylmethoxy)-
CBNumber:
CB61489712
Molecular Formula:
C14H11BrO3
Molecular Weight:
307.14
MDL Number:
MFCD04612889
MOL File:
62176-31-2.mol
MSDS File:
SDS
Last updated:2026-09-12 18:53:53

2-Benzyloxy-5-bromo-benzoic acid Properties

Melting point 106.1-107.4 °C
Boiling point 442.2±35.0 °C(Predicted)
Density 1.514±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
pka 3.09±0.36(Predicted)

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302-H315-H319-H335
Precautionary statements  P261-P305+P351+P338
HazardClass  IRRITANT

2-Benzyloxy-5-bromo-benzoic acid price More Price(30)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Biosynth FB119040 2-(Benzyloxy)-5-bromobenzoic acid 62176-31-2 1g $900 2026-06-04 Buy
Biosynth FB119040 2-(Benzyloxy)-5-bromobenzoic acid 62176-31-2 10g $900 2026-06-04 Buy
Biosynth FB119040 2-(Benzyloxy)-5-bromobenzoic acid 62176-31-2 0.5g $900 2026-06-04 Buy
Biosynth FB119040 2-(Benzyloxy)-5-bromobenzoic acid 62176-31-2 5g $900 2026-06-04 Buy
Biosynth FB119040 2-(Benzyloxy)-5-bromobenzoic acid 62176-31-2 25g $1233 2026-06-04 Buy
Product number Packaging Price Buy
FB119040 1g $900 Buy
FB119040 10g $900 Buy
FB119040 0.5g $900 Buy
FB119040 5g $900 Buy
FB119040 25g $1233 Buy

2-Benzyloxy-5-bromo-benzoic acid Chemical Properties,Uses,Production

Synthesis

2-BENZYLOXY-5-BROMO-BENZOIC ACID BENZYL ESTER

850350-09-3

2-BENZYLOXY-5-BROMO-BENZOIC ACID

62176-31-2

Benzyl 2-benzyloxy-5-bromobenzoate (18 g, 45.3 mmol) was used as starting material and dissolved in methanol (50 mL). Subsequently, a solution of sodium hydroxide (7.25 g, 181 mmol) in water (20.00 mL) was added to this solution. The reaction mixture was heated to 60°C and the reaction was stirred at this temperature for 2 hours. Upon completion of the reaction, the solvent was removed by rotary evaporation. The residue was diluted with water and washed with ethyl acetate (EA). The aqueous layer was separated and acidified to pH=3 with 4N hydrochloric acid solution and subsequently extracted with ethyl acetate (EA). The organic phases were combined, washed sequentially with water and saturated brine and dried over anhydrous sodium sulfate. Finally, the target product 2-(benzyloxy)-5-bromobenzoic acid (13.46 g, 97% yield) was obtained by concentration under reduced pressure.LCMS analysis showed [M+H]+ m/z 307,309.

References

[1] Bioorganic and Medicinal Chemistry Letters, 2019, vol. 29, # 2, p. 212 - 215
[2] Bioorganic and Medicinal Chemistry Letters, 2017, vol. 27, # 17, p. 4034 - 4038
[3] Patent: WO2011/38572, 2011, A1. Location in patent: Page/Page column 50

850350-09-3
62176-31-2
Synthesis of 2-Benzyloxy-5-bromo-benzoic acid from 2-Benzyloxy-5-bromo-benzoic acid benzyl ester

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Albb-008969 5-bromo-2-(phenylmethoxy)benzoic acid Benzoic acid, 5-bromo-2-(phenylmethoxy)- 62176-31-2