2,3,5,6-tetrafluoro-4-iodobenzaldehyde

98%

Reagent Code: #238934
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CAS Number 837368-26-0

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.98 g/mol
Formula C₇HIF₄O
inventory_2 Storage & Handling
Storage 2-8 °C, sealed, dry

description Product Description

Used primarily as a building block in the synthesis of advanced organic compounds, especially in pharmaceuticals and agrochemicals. Its unique structure with multiple fluorine atoms and an iodine substituent makes it valuable in medicinal chemistry for modifying drug potency and metabolic stability. The aldehyde group allows for easy functionalization, enabling coupling reactions such as Wittig or reductive amination to form more complex molecules. It is also employed in materials science, particularly in the development of fluorinated liquid crystals and organic electronic materials, where fluorine substitution enhances thermal and oxidative stability. The iodine moiety facilitates cross-coupling reactions like Suzuki or Heck reactions, expanding its utility in creating biaryl systems for functional molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,150.00
inventory 250mg
10-20 days ฿22,280.00
inventory 1g
10-20 days ฿58,810.00
2,3,5,6-tetrafluoro-4-iodobenzaldehyde
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Used primarily as a building block in the synthesis of advanced organic compounds, especially in pharmaceuticals and agrochemicals. Its unique structure with multiple fluorine atoms and an iodine substituent makes it valuable in medicinal chemistry for modifying drug potency and metabolic stability. The aldehyde group allows for easy functionalization, enabling coupling reactions such as Wittig or reductive amination to form more complex molecules. It is also employed in materials science, particularly i

Used primarily as a building block in the synthesis of advanced organic compounds, especially in pharmaceuticals and agrochemicals. Its unique structure with multiple fluorine atoms and an iodine substituent makes it valuable in medicinal chemistry for modifying drug potency and metabolic stability. The aldehyde group allows for easy functionalization, enabling coupling reactions such as Wittig or reductive amination to form more complex molecules. It is also employed in materials science, particularly in the development of fluorinated liquid crystals and organic electronic materials, where fluorine substitution enhances thermal and oxidative stability. The iodine moiety facilitates cross-coupling reactions like Suzuki or Heck reactions, expanding its utility in creating biaryl systems for functional molecules.

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