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Structure of 15112-62-6
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3-Iodo-2-methylpyridine features a sterically hindered iodopyridine core with a methyl group at the ortho position, enhancing regioselectivity in cross-coupling reactions. This bench-stable, moisture-tolerant heterocycle integrates efficiently into C–C and C–heteroatom bond formations, enabling streamlined access to complex pyridyl architectures in medicinal chemistry and materials synthesis.
3-Iodo-2-methylpyridine serves as a versatile building block in medicinal chemistry and catalytic cross-coupling reactions. The iodide group enables reliable Suzuki, Stille, and Negishi couplings, while the adjacent methylpyridine framework provides orthogonal reactivity for further functionalization. Bench-stable and readily purified by distillation or chromatography, it functions effectively in Pd-catalyzed transformations and is widely employed in the synthesis of heterocyclic scaffolds relevant to pharmaceutical development.
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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: