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Structure of 1211582-97-6
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2-Bromo-3-chloro-6-methylpyridine features a sterically accessible pyridine core bearing bromo and chloro substituents at adjacent positions, enabling efficient cross-coupling transformations. The methyl group enhances lipophilicity and provides a handle for further functionalization. This bench-stable, moisture-tolerant building block integrates readily into complex heterocyclic scaffolds under standard conditions.
2-Bromo-3-chloro-6-methylpyridine serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo group facilitates efficient Suzuki, Stille, or Negishi coupling, while the chloro and methyl functionalities offer site-selective functionalization. Bench-stable and readily purified by distillation, it functions reliably in the construction of complex pyridine-based scaffolds relevant to 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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: