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Structure of 170235-19-5
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Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate features a brominated pyridine core with orthogonal functional groups enabling direct coupling in cross-coupling reactions. The hydroxyl moiety offers a site for derivatization, while the ester group facilitates selective transformations. This bench-stable compound integrates readily into complex heterocyclic scaffolds under standard conditions.
Methyl 6-bromo-5-hydroxy-2-pyridinecarboxylate serves as a versatile building block in heterocyclic synthesis, enabling direct functionalization at the C5 hydroxyl and C6 bromide positions. The molecule exhibits bench stability and compatibility with palladium-catalyzed cross-coupling reactions, facilitating access to substituted pyridine scaffolds. Its dual reactive handles—electrophilic bromide and nucleophilically modifiable hydroxyl—support sequential transformations for medicinal chemistry applications.
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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: