3-Allyl-2-fluoro-4-iodopyridine

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Reagent Code: #66305
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CAS Number 340268-75-9

science Other reagents with same CAS 340268-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.05 g/mol
Formula C₈H₇FIN
badge Registry Numbers
MDL Number MFCD11501136
thermostat Physical Properties
Boiling Point 275.6±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active compounds. Its unique structure, featuring an allyl group, fluorine, and iodine atoms, makes it particularly valuable for constructing complex molecules that are often explored for their potential therapeutic properties. Researchers leverage its reactivity in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create novel drug candidates targeting specific diseases. Additionally, its fluorine and iodine substituents can enhance the metabolic stability and binding affinity of the resulting compounds, making it a valuable building block in medicinal chemistry. Beyond pharmaceuticals, it may also find use in material science for the development of advanced organic materials with tailored properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,148.00
inventory 250mg
10-20 days ฿10,305.00
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3-Allyl-2-fluoro-4-iodopyridine
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This chemical is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active compounds. Its unique structure, featuring an allyl group, fluorine, and iodine atoms, makes it particularly valuable for constructing complex molecules that are often explored for their potential therapeutic properties. Researchers leverage its reactivity in cross-coupling reactions, such as Suzuki or Sonogashira couplings, to create novel drug candidates targeting specific diseases. Additionally, its fluorine and iodine substituents can enhance the metabolic stability and binding affinity of the resulting compounds, making it a valuable building block in medicinal chemistry. Beyond pharmaceuticals, it may also find use in material science for the development of advanced organic materials with tailored properties.
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