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3-Bromo-5-fluoroanisole

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3-Bromo-5-fluoroanisole Basic information

Product Name:
3-Bromo-5-fluoroanisole
Synonyms:
  • 1-Bromo-3-fluoro-5-methoxybenzene, 3-Bromo-5-fluorophenyl methyl ether
  • 5-BROMO-3-FLUOROANISOLE
  • 3-BROMO-5-FLUOROANISOLE
  • 1-BROMO-3-FLUORO-5-METHOXYBENZENE
  • 1-broMo-3-fluoro-5-Methoxybenzene, 3-broMo-5-fluoroanisole, broMo-3-fluoro-5-Methoxy-benzene, 3-broMo-5-fluoro-anisole, 3-BroM-5-fluoranisol
  • 3-FLUORO-5-BROMO ANISOLE,=98%
  • 3-Bromo-5-fluoro-1-methoxybenzene
  • 3-Bromo-5-fluoroanis
CAS:
29578-39-0
MF:
C7H6BrFO
MW:
205.02
Product Categories:
  • Aromatic Halides (substituted)
Mol File:
29578-39-0.mol
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3-Bromo-5-fluoroanisole Chemical Properties

Boiling point:
94 °C / 17mmHg
Density 
1.59
refractive index 
1.5360-1.5400
storage temp. 
2-8°C
form 
clear liquid
color 
Colorless to Light yellow
Sensitive 
Light Sensitive
InChIKey
XVNQVSGOIUYOPB-UHFFFAOYSA-N
CAS DataBase Reference
29578-39-0(CAS DataBase Reference)
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Safety Information

Hazard Codes 
F,Xi,Xn
Risk Statements 
22
RIDADR 
1993
HazardClass 
IRRITANT
PackingGroup 
HS Code 
2909303890
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3-Bromo-5-fluoroanisole Usage And Synthesis

Chemical Properties

Colorless transparent liquid

Uses

3-fluoro-5-bromoanisole is an ether organic substance, which can be used as a pharmaceutical intermediate. 

Synthesis

461-96-1

124-41-4

29578-39-0

1. 1-Bromo-3,5-difluorobenzene (10 g, 0.052 mol) was dissolved in anhydrous DMF (300 mL) at 0-5 °C. 2. Sodium methanol (5.60 g, 0.1036 mol) was added to the above solution. 3. The reaction mixture was stirred at room temperature for 24 h. 4. Upon completion of the reaction, the reaction mixture was extracted three times with ethyl acetate. 5. The organic layers were combined, washed with brine and then dried with anhydrous Na2SO4. 6. The solvent was removed by evaporation to give 3-bromo-5-fluoroanisole (7.5 g, 71% yield).

References

[1] Patent: US2008/261941, 2008, A1. Location in patent: Page/Page column 43
[2] Bioorganic and Medicinal Chemistry, 2009, vol. 17, # 2, p. 758 - 766
[3] Journal of Medicinal Chemistry, 1997, vol. 40, # 11, p. 1634 - 1647

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