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Structure of 1211516-07-2
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2-Chloro-4-iodo-5-methoxypyridine features a pyridine core functionalized with chlorine, iodine, and methoxy groups at distinct positions, enabling selective cross-coupling reactions. The electron-deficient aromatic ring pairs with the reactive iodide for efficient Pd-catalyzed transformations. This scaffold offers high stability under standard conditions and facilitates rapid diversification in medicinal chemistry and agrochemical development.
2-Chloro-4-iodo-5-methoxypyridine serves as a versatile building block in cross-coupling chemistry, enabling the efficient construction of substituted pyridine scaffolds. The orthogonal reactivity of chlorine and iodine facilitates sequential functionalization, while the methoxy group offers mild directing effects and compatibility with standard reaction conditions. Its bench-stable nature and predictable coupling behavior make it well-suited for medicinal chemistry and process development 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: