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Structure of 41288-96-4
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2-Chloro-5-hydroxypyridine features a hydroxyl group positioned ortho to the chlorine substituent on a pyridine core, enabling direct functionalization at the C5 position. This arrangement facilitates nucleophilic substitution and coupling reactions under mild conditions, making it valuable for synthesizing bioactive heterocycles and advanced intermediates in medicinal chemistry.
2-Chloro-5-hydroxypyridine serves as a versatile building block in heterocyclic synthesis, enabling regioselective functionalization at the pyridine ring. The hydroxyl group facilitates direct coupling reactions or conversion to more reactive electrophiles, while the chlorine atom provides a reliable handle for palladium-catalyzed cross-coupling processes. Its bench-stable nature and compatibility with common protecting group strategies make it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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: