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Structure of 39919-65-8
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3,6-Dibromo-2-methylpyridine features a pyridine core substituted with bromine atoms at positions 3 and 6 and a methyl group at position 2. This electron-deficient heterocycle serves as a key building block in transition metal-catalyzed cross-coupling reactions, offering enhanced reactivity and selectivity in the synthesis of functionalized aryl systems.
3,6-Dibromo-2-methylpyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via cross-coupling reactions. The bromine atoms facilitate palladium-catalyzed transformations, while the methyl group provides a site for selective functionalization. Its bench-stable nature and compatibility with standard reaction conditions make it ideal for medicinal chemistry and process development workflows.
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GHS Pictogram :
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GHS No : GHS06
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Signal Word : Danger
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UN#: 2811
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Class : 6.1
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Packing Group : Ⅲ
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P302+P352-P304+P340
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Lot numbers can be found on the outside label of a product: