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4-Fluoro-2-(trifluoromethyl)benzyl bromide

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4-Fluoro-2-(trifluoromethyl)benzyl bromide Basic information

Product Name:
4-Fluoro-2-(trifluoromethyl)benzyl bromide
Synonyms:
  • 4-FLUORO-2-(TRIFLUOROMETHYL)BENZYL BROMIDE
  • ALPHA-BROMO-2-FLUORO-4-(TRIFLUOROMETHYL)TOLUENE
  • ALPHA-BROMO-4-FLUORO-2-(TRIFLUOROMETHYL)TOLUENE
  • 2-FLUORO-4-(TRIFLUOROMETHYL)BENZYL BROMIDE
  • 1-(BROMOMETHYL)-4-FLUORO-2-(TRIFLUOROMETHYL)BENZENE
  • a-Bromo-4-fluoro-2-(trifluoromethyl)toluene
  • 4-Fluoro-2-(trifluoromethyl)benzyl bromide, 97+%
  • à-bromo-4-fluoro-2-(trifluoromethyl)toluene
CAS:
206860-48-2
MF:
C8H5BrF4
MW:
257.02
EINECS:
625-261-3
Product Categories:
  • Aromatic Halides (substituted)
  • Aryl
  • Building Blocks
  • C8
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Organic Fluorinated Building Blocks
  • Trifluoromethyl
  • Fluoro-contained benzyl bromide series
Mol File:
206860-48-2.mol
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4-Fluoro-2-(trifluoromethyl)benzyl bromide Chemical Properties

Boiling point:
141 °C(lit.)
Density 
1.665 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.482(lit.)
Flash point:
185 °F
form 
Liquid
Specific Gravity
1.665
color 
Clear colorless to pale yellow
Sensitive 
Lachrymatory
CAS DataBase Reference
206860-48-2(CAS DataBase Reference)
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Safety Information

Hazard Codes 
C
Risk Statements 
34
Safety Statements 
26-27-36/37/39-45
RIDADR 
UN 2927 6.1/PG 2
WGK Germany 
3
Hazard Note 
Corrosive/Lachrymatory
HazardClass 
8
PackingGroup 
III
HS Code 
29039990

MSDS

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4-Fluoro-2-(trifluoromethyl)benzyl bromide Usage And Synthesis

Uses

4-Fluoro-2-(trifluoromethyl)benzyl bromide is a hydrocarbon halide that can be used as a pharmaceutical and chemical intermediate.

Chemical Properties

4-Fluoro-2-(trifluoromethyl)benzyl bromide is a colorless liquid with a density of 1.665 g/mL at 25 °C (lit.) and a boiling point of 141 °C (lit.).

Synthesis

Add 4-fluoro-2-(trifluoromethyl)benzenemethanol, tribromooxyphosphine and liquid bromine to a 100 mL three-necked flask equipped with an off-gas absorption device, a reflux condenser tube and a thermometer, and stir for 20 min at ambient temperature, and then heat the reaction system to 80 ??, and follow the thin-layer chromatography, and add a certain amount of saturated aqueous sodium bisulphite after the substrate has been completely involved in the reaction (about 1 h), and then wash out the unreacted liquid bromine. Then the upper layer of aqueous hydrogen bromide solution was separated. The organic phase was dried with anhydrous sodium sulfate and concentrated to obtain the crude product, which was eluted by the eluent of column chromatography purification (ethyl acetate: petroleum ether=1:20) and concentrated to obtain the colorless liquid 4-fluoro-2-(trifluoromethyl)benzyl bromide.

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