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Structure of 208519-41-9
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2-Chloro-6-(hydroxymethyl)pyridin-3-ol features a pyridine core functionalized with a chlorine atom and a hydroxymethyl group, enabling selective derivatization. The phenolic hydroxyl supports hydrogen bonding and enhances solubility, while the electron-withdrawing chlorine imparts reactivity for cross-coupling or nucleophilic substitution. This bench-stable scaffold integrates readily into bioactive molecule synthesis.
2-Chloro-6-(hydroxymethyl)pyridin-3-ol serves as a versatile building block in medicinal chemistry, enabling efficient access to pyridine-based pharmacophores. The molecule combines a reactive chloro group for nucleophilic substitution and a pendant hydroxymethyl function for oxidation or derivatization. Its bench-stable nature and compatibility with standard coupling protocols facilitate streamlined synthesis of heterocyclic intermediates and API candidates.
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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: