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Structure of 30766-12-2
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Methyl 5-hydroxypyridine-2-carboxylate features a hydroxyl group at the 5-position and an ester-functionalized pyridine ring, enabling direct incorporation into heterocyclic synthesis. The electron-rich pyridine core supports efficient metal-catalyzed coupling reactions, while the pendant hydroxyl offers sites for derivatization or hydrogen bonding in molecular recognition systems.
Methyl 5-hydroxypyridine-2-carboxylate serves as a versatile building block in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds. The ortho-hydroxyester functionality facilitates directed metalation and subsequent functionalization, while the methyl ester supports straightforward derivatization via hydrolysis or reduction. Bench-stable and compatible with common coupling protocols, it functions effectively in medicinal chemistry campaigns requiring pyridine-based pharmacophores.
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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: