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3-Bromofluorobenzene

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3-Bromofluorobenzene Basic information

Product Name:
3-Bromofluorobenzene
Synonyms:
  • M-BROMOFLUOROBENZENE
  • 1-BROMO-3-FLUOROBENZENE
  • 3-FLUOROBROMOBENZENE
  • 3-BROMOFLUOROBENZENE
  • M-FLUOROBROMOBENZENE
  • 3-Fluorobromobenzene 99%
  • BroMo between fluoride
  • 3-BroMofluorobenzene, 99% 25ML
CAS:
1073-06-9
MF:
C6H4BrF
MW:
175
EINECS:
214-023-0
Product Categories:
  • Benzene series
  • Fluorobenzene
  • Aromatic Hydrocarbons (substituted) & Derivatives
  • alkyl bromide| alkyl Fluorine
  • Pyridines
  • Aryl
  • Halogenated Hydrocarbons
  • Bromine Compounds
  • Fluorine Compounds
  • Fluorobenzene Series
  • C6
Mol File:
1073-06-9.mol
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3-Bromofluorobenzene Chemical Properties

Melting point:
-8°C
Boiling point:
149-151 °C(lit.)
Density 
1.567 g/mL at 25 °C(lit.)
refractive index 
n20/D 1.526(lit.)
Flash point:
102 °F
storage temp. 
Sealed in dry,Room Temperature
solubility 
0.4g/l
form 
Liquid
Specific Gravity
1.567
color 
Clear colorless to light yellow
Water Solubility 
insoluble
BRN 
1853969
InChIKey
QDFKKJYEIFBEFC-UHFFFAOYSA-N
CAS DataBase Reference
1073-06-9(CAS DataBase Reference)
NIST Chemistry Reference
Benzene, 1-bromo-3-fluoro-(1073-06-9)
EPA Substance Registry System
Benzene, 1-bromo-3-fluoro- (1073-06-9)
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Safety Information

Hazard Codes 
Xn,F,Xi
Risk Statements 
10-22-36/38-36/37/38-20/21/22
Safety Statements 
26-36-37/39-16
RIDADR 
UN 1993 3/PG 3
WGK Germany 
2
RTECS 
DA1225000
Hazard Note 
Flammable/Irritant
TSCA 
Yes
HazardClass 
3
PackingGroup 
III
HS Code 
29036990

MSDS

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3-Bromofluorobenzene Usage And Synthesis

Chemical Properties

Clearcolourlesstolightyellowliqui

Uses

Intermediates of Liquid Crystals

Synthesis

1430342-19-0

1073-06-9

The general procedure for the synthesis of m-bromofluorobenzene from the compound (CAS: 1430342-19-0) is as follows: a mixture of diaryliodonium salt (0.5 mmol), methylene halide (0.75 mmol) and acetonitrile (1 mL) was added to a 10 mL reaction tube and heated at 80 °C for 2 h with vigorous stirring. After completion of the reaction (monitored by TLC or GC), the reaction mixture was cooled to room temperature and 5 mL of water was added. After stirring for 10 min, the product was extracted with ethyl acetate (3 x 10 mL). The organic layers were combined, washed with water and dried with anhydrous sodium sulfate. The solvent was evaporated under reduced pressure to give the crude product. The crude product was purified by silica gel column chromatography using petroleum ether and ethyl acetate as eluents to give purified m-bromofluorobenzene. The structure of the product was confirmed by 1H NMR and 13C NMR.

References

[1] Letters in Organic Chemistry, 2013, vol. 10, # 8, p. 541 - 548

3-Bromofluorobenzene Preparation Products And Raw materials

Preparation Products

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