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Structure of 1227592-89-3
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2-Chloro-4-iodo-6-methylpyridine features a trifunctional pyridine core with complementary halogen handles, enabling sequential cross-coupling reactions. The chlorine and iodine substituents facilitate orthogonal reactivity in palladium-catalyzed transformations, while the methyl group enhances solubility and electronic modulation. This bench-stable derivative serves as a key building block for bioactive heterocycles and advanced pharmaceutical intermediates.
2-Chloro-4-iodo-6-methylpyridine serves as a versatile building block in cross-coupling chemistry, enabling efficient Suzuki, Stille, and Negishi reactions due to its orthogonal halogen reactivity. The chloro group exhibits high stability under standard reaction conditions, while the iodo substituent facilitates rapid coupling with boronic acids and organometallics. Its methyl group provides a convenient handle for further functionalization, and the molecule demonstrates excellent bench stability and ease of purification—ideal for iterative synthesis of complex heterocyclic scaffolds and pharmaceutical intermediates.
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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: