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Structure of 42330-59-6
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2-Chloro-3-(hydroxymethyl)pyridine features a reactive chloropyridine core paired with a pendant hydroxymethyl group, enabling seamless functionalization in synthetic transformations. This bench-stable derivative integrates readily into heterocyclic scaffolds and serves as a key intermediate in medicinal chemistry and agrochemical development.
2-Chloro-3-(hydroxymethyl)pyridine serves as a versatile building block in medicinal chemistry, enabling efficient functionalization at the pyridine ring via nucleophilic substitution. The chloro group exhibits high reactivity toward amines, thiols, and other nucleophiles under mild conditions, while the hydroxymethyl moiety provides a handle for oxidation, protection, or further derivatization. Its bench-stable nature and compatibility with standard synthetic workflows make it ideal for constructing heterocyclic scaffolds and API intermediates.
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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: