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Structure of 1256810-64-6
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2-Bromo-4-chloro-5-methoxypyridine features a pyridine core functionalized with bromo, chloro, and methoxy groups at strategic positions, enabling selective coupling reactions. The electron-deficient ring facilitates cross-coupling under palladium catalysis, while the methoxy group enhances solubility and modulates reactivity. This compound serves as a key building block in pharmaceutical synthesis and agrochemical development.
2-Bromo-4-chloro-5-methoxypyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its orthogonal halogen reactivity. The methoxy group enhances solubility and modulates electronic properties, while the bromo and chloro substituents allow sequential functionalization under selective catalytic conditions. Its bench-stable, crystalline nature facilitates handling and purification in multi-step syntheses.
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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: