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Structure of 73112-16-0
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2,6-Dibromo-4-methylpyridine features a pyridine core with strategically positioned bromine atoms and a methyl group, enabling selective functionalization in cross-coupling reactions. The electron-deficient ring facilitates palladium-catalyzed transformations, while the steric protection from the methyl substituent enhances regioselectivity. This compound serves as a key building block for bioactive heterocycles and advanced materials.
2,6-Dibromo-4-methylpyridine serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via palladium-catalyzed cross-coupling reactions. The ortho-bromine substituents provide high reactivity in Suzuki, Stille, and Negishi couplings, while the methyl group enhances electronic modulation and metabolic stability in downstream applications. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses for medicinal chemistry and agrochemical 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: