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Structure of 1256819-37-0
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2-Bromo-6-chloro-3-methoxypyridine features a halogenated pyridine core with complementary reactivity at the bromo and chloro sites, enabling selective cross-coupling transformations. The methoxy group enhances solubility and modulates electronic properties, supporting efficient derivatization in medicinal chemistry and materials synthesis under standard conditions.
2-Bromo-6-chloro-3-methoxypyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The bromo group facilitates Suzuki, Stille, or Negishi coupling, while the chloro and methoxy substituents provide steric and electronic modulation. Bench-stable and readily purified by column chromatography, it supports efficient synthesis of substituted pyridine scaffolds relevant to pharmaceutical discovery.
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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: