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2-Bromo-3-fluoroanisole

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Products Intro: Product Name:2-Bromo-3-fluoroanisole
CAS:446-59-3
Purity:99% Package:1KG;8USD|1000KG;0.8USD
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Products Intro: Product Name:Benzene, 2-bromo-1-fluoro-3-methoxy-
CAS:446-59-3
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Products Intro: Product Name:2-Bromo-1-fluoro-3-methoxybenzene
CAS:446-59-3
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Products Intro: Product Name:2-Bromo-3-fluoroanisole
CAS:446-59-3
Purity:0.98 Package:1g;5g;25g;100;500g
Company Name: Shenzhen Excellent Biotech Co., Ltd.
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Products Intro: Product Name:2-bromo-3-fluoroanisole
CAS:446-59-3
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2-Bromo-3-fluoroanisole manufacturers

  • 2-Bromo-3-fluoroanisole
  • 2-Bromo-3-fluoroanisole pictures
  • $8.00 / 1KG
  • 2025-09-25
  • CAS:446-59-3
  • Min. Order: 1KG
  • Purity: 99%
  • Supply Ability: g-kg-tons, free sample is available
2-Bromo-3-fluoroanisole Basic information
Product Name:2-Bromo-3-fluoroanisole
Synonyms:BENZENE,2-BROMO-1-FLUORO-3-METHOXY;REF DUPL: 2-bromo-3-fluoroanisole;Bromo-3-fluoro anisole;2-BROMO-3-FLUOROANISOLE;2-Bromo-1-fluoro-3-methoxy-benzene;2-Bromo-3-fluoroanisole 99%;2-Bromo-3-fluoroanisole99%;2-Bromo-1-fluoro-3-methoxybenzene, 2-Bromo-3-fluorophenyl methyl ether
CAS:446-59-3
MF:C7H6BrFO
MW:205.02
EINECS:
Product Categories:Aromatic Halides (substituted)
Mol File:446-59-3.mol
2-Bromo-3-fluoroanisole Structure
2-Bromo-3-fluoroanisole Chemical Properties
Boiling point 189.2±20.0 °C(Predicted)
density 1.531±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
form crystals
color Off-white
CAS DataBase Reference446-59-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
HazardClass IRRITANT
HS Code 2909303890
MSDS Information
2-Bromo-3-fluoroanisole Usage And Synthesis
Uses2-Bromo-3-fluoroanisole is a phenyl ether compound with fluorine and bromine functional groups on the benzene ring, which can be used as an organic synthesis raw material or intermediate.
Synthesis
2-Bromo-3-fluorophenol

443-81-2

Iodomethane

74-88-4

2-Bromo-3-fluoroanisole

446-59-3

GENERAL METHOD: 2-Bromo-3-fluorophenol (0.1 mol) was dissolved in DMF (100 mL) and K2CO3 (0.1 mol) and iodomethane (0.1 mol) were added sequentially. The reaction mixture was stirred at room temperature for 24 hours. Upon completion of the reaction, water (400 mL) was added to dilute and the mixture was extracted with hexane. The organic phases were combined, washed with water, dried over anhydrous sodium sulfate, filtered through a silica plug and concentrated under reduced pressure to give 2-bromo-3-fluoroanisole.

References[1] European Journal of Medicinal Chemistry, 2015, vol. 89, p. 524 - 539
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