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Structure of 13210-29-2
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1-(3-Hydroxypyridin-2-yl)ethanone features a pyridinone scaffold with a pendant ketone, enabling direct integration into heterocyclic synthesis. The hydroxyl group supports hydrogen bonding and enhances solubility in polar solvents, while the carbonyl facilitates nucleophilic addition and condensation reactions under standard conditions. This compound serves as a key intermediate for bioactive molecule construction.
1-(3-Hydroxypyridin-2-yl)ethanone serves as a versatile building block for heterocyclic synthesis, enabling efficient access to pyridine-based scaffolds through standard functional group transformations. Its hydroxypyridine moiety provides orthogonal reactivity for derivatization, while the acetyl group facilitates electrophilic substitution and condensation reactions. The compound exhibits good bench stability and compatibility with common purification techniques, making it well-suited for iterative synthetic workflows in medicinal chemistry and process development.
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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: