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Structure of 65550-77-8
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2-Bromo-5-chloro-3-methylpyridine features a sterically accessible pyridine core bearing strategically positioned halogen and methyl groups, enabling direct functionalization in cross-coupling reactions. The electron-deficient ring facilitates palladium-catalyzed transformations, while the ortho-halogen arrangement supports selective derivatization. This bench-stable reagent integrates efficiently into complex heterocyclic synthesis workflows.
2-Bromo-5-chloro-3-methylpyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromine site undergoes efficient Suzuki, Stille, or Negishi coupling, while the chlorine remains inert under standard conditions, facilitating sequential functionalization. Bench-stable and readily purified by distillation, it supports scalable synthesis of substituted pyridines relevant to agrochemicals 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: