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3,5-Difluorobenzyl bromide

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3,5-Difluorobenzyl bromide Basic information

Product Name:
3,5-Difluorobenzyl bromide
Synonyms:
  • 1-(BROMOMETHYL)-3,5-DIFLUOROBENZENE
  • 3,5-DIFLUOROBENZYL BROMIDE
  • ALPHA-BROMO-3,5-DIFLUOROTOLUENE
  • à-bromo-3,5-difluorotoluene
  • α-bromo-3,5-difluorotoluene
  • 3,5-Difluorobenzyl bromide 98%
  • 3,5-Difluorobenzylbromide98%
  • 2-Benzyloxy-5-formylphenylboronic acid
CAS:
141776-91-2
MF:
C7H5BrF2
MW:
207.02
EINECS:
627-819-1
Product Categories:
  • Aryl Fluorinated Building Blocks
  • C7
  • Chemical Synthesis
  • Fluorinated Building Blocks
  • Halogenated Hydrocarbons
  • Organic Building Blocks
  • Organic Fluorinated Building Blocks
  • Other Fluorinated Organic Building Blocks
  • Fluorine series
  • Aromatic Halides (substituted)
  • Miscellaneous
  • Aryl
  • Organohalides
  • Catalysts-Ligands
  • Organoborons
  • Sulfonamide
  • Amide
  • Building Blocks
  • Fluorinated
  • Boronic ester
  • Boronic acid
  • Alkoxy
  • Ester
  • Fluoro-contained benzyl bromide series
Mol File:
141776-91-2.mol
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3,5-Difluorobenzyl bromide Chemical Properties

Boiling point:
65 °C4.5 mm Hg(lit.)
Density 
1.6 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.521(lit.)
Flash point:
179 °F
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
form 
clear liquid
color 
Colorless to Orange to Green
Specific Gravity
1.62
Sensitive 
Lachrymatory
BRN 
7422062
InChI
InChI=1S/C7H5BrF2/c8-4-5-1-6(9)3-7(10)2-5/h1-3H,4H2
InChIKey
KVSVNRFSKRFPIL-UHFFFAOYSA-N
SMILES
C1(CBr)=CC(F)=CC(F)=C1
CAS DataBase Reference
141776-91-2(CAS DataBase Reference)
NIST Chemistry Reference
3,5-Difluorobenzyl bromide(141776-91-2)
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Safety Information

Hazard Codes 
C,Xi
Risk Statements 
34-36-43
Safety Statements 
26-36/37/39-45-27-36/37
RIDADR 
UN 3265 8/PG 2
WGK Germany 
3
Hazard Note 
Corrosive/Lachrymatory
HazardClass 
8
PackingGroup 
III
HS Code 
29039990
Storage Class
8A - Combustible corrosive hazardous materials
Hazard Classifications
Skin Corr. 1B

MSDS

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3,5-Difluorobenzyl bromide Usage And Synthesis

Chemical Properties

Colorless to light yellow liqui

Uses

3,5-Difluorobenzyl bromide is a kind of important medicine intermediate. 

Synthesis

Triphenylphosphine (2.75 g, 10.5 mmol) and carbon tetrabromide (3.48 g, 10.5 mmol) were added to a dry reaction flask followed by the addition of 25 mL of ether and the resulting mixture was stirred at room temperature for 30 min, then an ether solution of 3,5-difluorobenzenemethanol (10.5 mmol) was slowly added to the above mentioned system and the reaction mixture was continued to be stirred at 25??C for 40 minutes. At the end of the reaction, petroleum ether was added to the reaction system, and a white precipitate of triphenylphosphine oxide was observed. Most of the triphenylphosphine oxide was removed by filtration, and the obtained filtrate was concentrated in vacuum, and finally, hexane was used as the eluent, and the residue was separated and purified by silica gel chromatography to obtain the target product of 3,5-difluorobenzyl bromide.

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