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Structure of 213771-32-5
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Methyl 5-bromo-3-methylpyridine-2-carboxylate features a pyridine core functionalized with bromo, methyl, and ester groups at strategic positions. This trifunctional scaffold enables direct coupling in cross-coupling reactions and serves as a key intermediate in the synthesis of bioactive heterocycles and pharmaceutical candidates. The molecule exhibits enhanced stability under standard bench conditions and compatibility with transition metal catalysis.
Methyl 5-bromo-3-methylpyridine-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling palladium-catalyzed cross-coupling reactions at the bromo position. The methyl and ester groups provide orthogonal functionality for further derivatization, while the pyridine core offers favorable electronic properties for medicinal chemistry applications. Bench-stable and readily purified by column chromatography, it facilitates efficient access to substituted pyridine scaffolds relevant to agrochemical and pharmaceutical development.
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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: