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

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Reagent Code: #79124
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CAS Number 1321963-74-9

science Other reagents with same CAS 1321963-74-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.00 g/mol
Formula C₇H₃F₄IO
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MDL Number MFCD20526760
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed away from light

description 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.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,854.00
inventory 250mg
10-20 days ฿2,781.00
inventory 1g
10-20 days ฿6,939.00

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

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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