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Structure of 1020253-15-9
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4-Bromo-2-chloro-5-methoxypyridine is a halogenated pyridine derivative featuring strategically positioned bromo, chloro, and methoxy substituents. This combination enables selective functionalization in cross-coupling reactions, serving as a key intermediate in the synthesis of bioactive heterocycles. The molecule exhibits enhanced stability under standard conditions and facilitates efficient derivatization in medicinal chemistry workflows.
4-Bromo-2-chloro-5-methoxypyridine serves as a versatile building block in medicinal chemistry and 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 methoxy substituents provide steric and electronic control. This compound exhibits excellent bench stability and is readily purified by flash chromatography, making it ideal for scalable synthesis of complex pyridine-based scaffolds.
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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: