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Structure of 1402666-66-3
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6-Bromo-3-methyl-pyridine-2-carboxylic acid methyl ester features a brominated pyridine core with strategically positioned methyl and ester groups, enabling direct functionalization in cross-coupling and heterocyclic synthesis. This bench-stable derivative facilitates efficient access to complex nitrogen-containing scaffolds under standard conditions.
6-Bromo-3-methyl-pyridine-2-carboxylic acid methyl ester serves as a versatile building block in medicinal chemistry, enabling efficient construction of pyridine-based scaffolds. The bromo group facilitates palladium-catalyzed cross-coupling reactions, while the ester and methyl functionalities offer orthogonal handles for further derivatization. Bench-stable and amenable to standard purification methods, it functions reliably in multi-step synthesis workflows requiring precise regiocontrol.
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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: