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Structure of 79055-50-8
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2,4-Dibromo-5-methylpyridine features a pyridine core substituted with bromine atoms at the 2- and 4-positions and a methyl group at the 5-position, delivering enhanced electrophilicity for cross-coupling reactions. The para-bromo and ortho-bromo sites enable selective functionalization in palladium-catalyzed transformations, while the methyl group provides steric and electronic modulation. This scaffold integrates efficiently into complex heterocyclic architectures under standard conditions.
2,4-Dibromo-5-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined halogen positions. The methyl group enhances regioselectivity in electrophilic substitution, while the dibromopyridine core provides orthogonal reactivity for sequential functionalization. Bench-stable and compatible with standard purification techniques, it facilitates efficient construction of complex heterocyclic scaffolds in multi-step syntheses.
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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: