Basic information Safety Supplier Related

3-BROMO-4-FLUOROBENZYL BROMIDE

Basic information Safety Supplier Related

3-BROMO-4-FLUOROBENZYL BROMIDE Basic information

Product Name:
3-BROMO-4-FLUOROBENZYL BROMIDE
Synonyms:
  • 2-BroMo-4-(broMoMethyl)-1-fluorobenzene
  • 2-Bromo-4-(bromomethyl)-1-fluorobenzene, alpha,3-Dibromo-4-fluorotoluene
  • 3-Bromo-4-fluorobenzyl Bromide >
  • Benzene, 2-bromo-4-(bromomethyl)-1-fluoro-
CAS:
78239-71-1
MF:
C7H5Br2F
MW:
267.92
Mol File:
78239-71-1.mol
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3-BROMO-4-FLUOROBENZYL BROMIDE Chemical Properties

Melting point:
41 °C
Boiling point:
259.8±25.0 °C(Predicted)
Density 
1.923±0.06 g/cm3(Predicted)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
soluble in Methanol
form 
Solid
color 
White
Water Solubility 
Slightly soluble in water.
Sensitive 
Lachrymatory
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Safety Information

Hazard Codes 
C,T
RIDADR 
3261
HazardClass 
8
PackingGroup 
II
HS Code 
2903998090
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3-BROMO-4-FLUOROBENZYL BROMIDE Usage And Synthesis

Uses

3-Bromo-4-fluorobenzyl bromide is used as a pharmaceutical intermediate.

Synthesis

452-62-0

78239-71-1

General procedure for the synthesis of 3-bromo-4-fluorobenzyl bromide from 3-bromo-4-fluorotoluene: 3-bromo-4-fluorotoluene (6 mL, 48 mmol) and N-bromosuccinimide (2.7 g, 15 mmol) were dissolved in 1,2-dichloroethane, followed by the addition of 2,2'-azobisisobutyronitrile (16 mg, 0.1 mmol) to a 1,2-dichloroethane solution ( 10 mL). The reaction mixture was heated to reflux for 2 hours. After completion of the reaction, it was cooled to room temperature, diluted with 1,2-dichloroethane (40 mL) and washed with water (2 x 50 mL). The organic phase was dried over anhydrous magnesium sulfate and concentrated to a small volume under reduced pressure. The product 3-bromo-4-fluorobenzyl bromide was obtained (yield: 9.2 g, 72% yield).

References

[1] Patent: US2009/69320, 2009, A1. Location in patent: Page/Page column 71
[2] Journal of medicinal chemistry, 1967, vol. 10, # 1, p. 64 - 66
[3] Patent: US6586633, 2003, B1

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