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Structure of 1214345-48-8
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This hydroxypyridine-acetic acid derivative integrates a polar hydroxyl group and a carboxylic acid functionality, enabling versatile conjugation and metal chelation. The electron-rich pyridine ring enhances reactivity in transition-metal-catalyzed coupling processes. Designed for synthetic flexibility in medicinal chemistry and materials science applications.
2-(5-Hydroxypyridin-2-yl)acetic acid serves as a versatile building block for heterocyclic synthesis, enabling efficient access to bioactive pyridine derivatives. Its hydroxyl and carboxylic acid functionalities provide orthogonal handles for derivatization, including esterification, amidation, and metal-catalyzed coupling reactions. The molecule exhibits good bench stability and facilitates straightforward purification, making it well-suited for medicinal chemistry campaigns and process development workflows.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: