2-Fluoroiodobenzene

99%, with 0.01% copper stabilizer

  • Product Code: 123266
  Alias:    o-Fluoroiodobenzene ; 2-Fluoroiodobenzene
  CAS:    348-52-7
Molecular Weight: 222 g./mol Molecular Formula: C₆H₄FI
EC Number: 206-477-3 MDL Number: MFCD00001031
Melting Point: −41-−40 °C(lit.) Boiling Point: 188-189 °C(lit.)
Density: 1.903 g/mL at 25 °C(lit.) Storage Condition: Room temperature, away from light, dry
Product Description: 2-Fluoroiodobenzene is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both fluorine and iodine atoms, makes it valuable for introducing fluorinated aromatic rings into complex molecules, which is crucial in drug design to enhance metabolic stability and bioavailability. Additionally, it serves as a key reagent in cross-coupling reactions, such as the Suzuki-Miyaura and Ullmann reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds. This compound is also employed in the synthesis of liquid crystals and advanced materials, where its electronic properties are leveraged for specific applications.
Product Specification:
Test Specification
Purity (GC) 99-100
Refractive Index N20/D 1.5899-1.5919
Specific Gravity (20/20 Degree Celsius) 1.93-1.935
Appearance Colorless Liquid
Infrared Spectrum Conforms To Structure
Stabilizer Copper
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
5.000 10-20 days ฿280.00
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25.000 10-20 days ฿790.00
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100.000 10-20 days ฿2,760.00
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500.000 10-20 days ฿12,560.00
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2-Fluoroiodobenzene
2-Fluoroiodobenzene is primarily used as a versatile intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both fluorine and iodine atoms, makes it valuable for introducing fluorinated aromatic rings into complex molecules, which is crucial in drug design to enhance metabolic stability and bioavailability. Additionally, it serves as a key reagent in cross-coupling reactions, such as the Suzuki-Miyaura and Ullmann reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds. This compound is also employed in the synthesis of liquid crystals and advanced materials, where its electronic properties are leveraged for specific applications.
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