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Structure of 58481-10-0
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2-Iodopyridine-4-carboxylic acid features a strategically positioned iodine atom and carboxylic acid group on the pyridine ring, enabling direct functionalization in cross-coupling reactions. This dual-functional scaffold integrates readily into bioactive molecules and serves as a key building block in medicinal chemistry and materials science.
2-Iodopyridine-4-carboxylic acid serves as a versatile building block for C–H functionalization and cross-coupling reactions, enabling efficient access to substituted pyridine scaffolds. The iodide group facilitates palladium-catalyzed coupling with arylboranes, alkenes, and heteroatom nucleophiles, while the carboxylic acid functions as a handle for derivatization or metal complexation. Its bench-stable crystalline form supports straightforward handling and purification in synthetic workflows.
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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: