2-Fluoro-1-iodo-4-(trifluoromethoxy)benzene

95%

  • Product Code: 79124
  CAS:    1321963-74-9
Molecular Weight: 306.00 g./mol Molecular Formula: C₇H₃F₄IO
EC Number: MDL Number: MFCD20526760
Melting Point: Boiling Point:
Density: Storage Condition: Room temperature, dry and sealed away from light
Product Description: This compound is primarily utilized in organic synthesis as a versatile building block for the development of complex molecules. Its unique structure, featuring both fluorine and iodine substituents, makes it a valuable intermediate in cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in the production of pharmaceuticals and agrochemicals. The trifluoromethoxy group enhances the lipophilicity and metabolic stability of the resulting compounds, making it particularly useful in drug discovery for designing molecules with improved bioavailability. Additionally, it serves as a precursor in the synthesis of advanced materials, including liquid crystals and polymers, where its fluorine-containing groups contribute to desirable properties like thermal stability and chemical resistance.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $76.99
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0.250 10-20 days $115.49
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1.000 10-20 days $288.17
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2-Fluoro-1-iodo-4-(trifluoromethoxy)benzene
This compound is primarily utilized in organic synthesis as a versatile building block for the development of complex molecules. Its unique structure, featuring both fluorine and iodine substituents, makes it a valuable intermediate in cross-coupling reactions, such as Suzuki and Sonogashira couplings, which are essential in the production of pharmaceuticals and agrochemicals. The trifluoromethoxy group enhances the lipophilicity and metabolic stability of the resulting compounds, making it particularly useful in drug discovery for designing molecules with improved bioavailability. Additionally, it serves as a precursor in the synthesis of advanced materials, including liquid crystals and polymers, where its fluorine-containing groups contribute to desirable properties like thermal stability and chemical resistance.
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