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Structure of 21543-49-7
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2-Chloro-5-hydroxymethylpyridine features a pyridine core functionalized with chlorine at the 2-position and a hydroxymethyl group at the 5-position, enabling direct coupling or derivatization in synthetic workflows. This bifunctional architecture supports efficient incorporation into pharmaceutical intermediates and ligand frameworks, where the hydroxymethyl moiety offers a site for further modification while maintaining compatibility with standard reaction conditions.
2-Chloro-5-hydroxymethylpyridine serves as a versatile building block in medicinal chemistry, enabling site-specific functionalization via the reactive chloro and hydroxymethyl groups. The hydroxymethyl moiety facilitates direct oxidation to carboxylic acid or ether formation, while the chlorine supports palladium-catalyzed cross-coupling reactions. Its bench-stable nature and compatibility with common protecting group strategies make it ideal for constructing heterocyclic scaffolds and API intermediates in multi-step syntheses.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: