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Structure of 851386-34-0
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2,3-Difluoro-4-iodopyridine is a fluorinated heteroaryl iodide featuring strategic electronic tuning via adjacent fluorine atoms. This bench-stable scaffold enables efficient cross-coupling reactions, particularly in palladium-catalyzed transformations. The electron-deficient pyridine ring enhances reactivity in C–X bond formation, while the iodide group provides high functional group tolerance and predictable coupling efficiency. Ideal for constructing complex molecular architectures in medicinal chemistry and materials science.
2,3-Difluoro-4-iodopyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive iodide handle. The difluoro substitution pattern enhances metabolic stability and modulates electronic properties, while the pyridine core provides a robust scaffold for drug discovery. Its bench-stable nature and compatibility with standard coupling conditions facilitate efficient synthesis of complex heterocyclic architectures.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: