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Home  > 3,5-Difluoro-4-iodopyridine

AE16263

1116099-07-0 | 3,5-Difluoro-4-iodopyridine

Packsize Purity Availability Price Discounted Price    Quantity
100mg 95% in stock $48.00 $33.00 -   +
250mg 95% in stock $78.00 $54.00 -   +
1g 95% in stock $93.00 $65.00 -   +
5g 95% in stock $332.00 $232.00 -   +
25g 95% in stock $1,317.00 $922.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AE16263
Chemical Name: 3,5-Difluoro-4-iodopyridine
CAS Number: 1116099-07-0
Molecular Formula: C5H2F2IN
Molecular Weight: 240.9774
MDL Number: MFCD13185558
SMILES: Fc1cncc(c1I)F

 

Upstream Synthesis Route
  • 3,5-Difluoro-4-iodopyridine is a versatile chemical compound that finds wide application in chemical synthesis processes. This compound serves as a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure, featuring both fluorine and iodine substituents, imparts distinct reactivity and properties that are crucial in a range of synthetic pathways.In organic synthesis, 3,5-Difluoro-4-iodopyridine can act as a key intermediate for the introduction of fluorine and iodine functionalities into target molecules. The presence of fluorine atoms in the molecule can enhance the bioavailability, metabolic stability, and binding affinity of pharmaceutical compounds. Additionally, the iodine substituent facilitates further functionalization through cross-coupling reactions, such as Suzuki-Miyaura and Heck couplings, enabling the construction of complex molecular architectures.Furthermore, 3,5-Difluoro-4-iodopyridine is employed in the preparation of heterocyclic compounds, which are essential scaffolds in medicinal chemistry and material science. By judiciously incorporating this fluorinated and iodinated pyridine derivative into synthetic routes, chemists can access structurally diverse compounds with tailored properties for specific applications. Overall, the strategic utilization of 3,5-Difluoro-4-iodopyridine in chemical synthesis endeavors enables the efficient and controlled construction of molecules with enhanced functionality and biological activity.
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