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3-FLUORO-4-IODOTOLUENE

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3-FLUORO-4-IODOTOLUENE Basic information

Product Name:
3-FLUORO-4-IODOTOLUENE
Synonyms:
  • BUTTPARK 148\01-16
  • 4-IODO-3-FLUOROTOLUENE
  • 3-FLUORO-4-IODOTOLUENE
  • Benzene, 2-fluoro-1-iodo-4-methyl-
  • 3-FLUORO-4-IODOTOLUENE ISO 9001:2015 REACH
CAS:
452-79-9
MF:
C7H6FI
MW:
236.03
Product Categories:
  • Fluorine Compounds
  • Iodine Compounds
  • Aryl
  • C7
  • Halogenated Hydrocarbons
  • Aromatic Halides (substituted)
  • Halogen toluene
  • Fluoro-contained Iodo series
Mol File:
452-79-9.mol
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3-FLUORO-4-IODOTOLUENE Chemical Properties

Boiling point:
138-139 °C/9 mmHg (lit.)
Density 
1.803 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.5810(lit.)
Flash point:
199 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
Appearance
Pink to red Liquid
Sensitive 
Light Sensitive
CAS DataBase Reference
452-79-9(CAS DataBase Reference)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
52/53
Safety Statements 
23-24/25-61-60
WGK Germany 
3
Hazard Note 
Irritant
HS Code 
29039990

MSDS

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3-FLUORO-4-IODOTOLUENE Usage And Synthesis

Chemical Properties

colorless to light yellow liqui

Synthesis

452-74-4

452-79-9

A solution was prepared by dissolving 4-bromo-3-fluorotoluene (10 g) in tetrahydrofuran (THF, 50 mL) under a dry nitrogen atmosphere and cooled to -72 °C. Subsequently, a hexane solution (35 mL) of 1.6 M n-butyllithium was slowly added at -72 °C, the reaction temperature was controlled not to exceed -65 °C and stirring was continued for 1 h at this temperature. A solution prepared by dissolving iodine (14.8 g) in THF (30 mL) was added to the above reaction mixture at -72 °C, ensuring that the internal temperature was not higher than -60 °C, after which it was slowly warmed to room temperature. Upon completion of the reaction, saturated aqueous ammonium chloride solution and hexane were added to the mixture to separate the organic layer. The organic layer was sequentially washed twice with 10% aqueous sodium sulfite, then with saturated brine and finally dried with anhydrous sodium sulfate. The desiccant was removed by filtration and the organic solvent was removed by distillation under reduced pressure. The residue was purified by silica gel column chromatography to give 13.0 g of 3-fluoro-4-iodotoluene as a yellow liquid.

References

[1] Patent: US2014/275577, 2014, A1. Location in patent: Paragraph 0166; 0167

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