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Structure of 86869-14-9
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2-Cyano-5-hydroxypyridine features a strategically positioned hydroxyl group and nitrile moiety on a pyridine scaffold, enabling direct functionalization in synthetic transformations. The electron-deficient ring facilitates nucleophilic substitution, while the hydroxyl group offers a handle for derivatization under mild conditions. This compound serves as a key intermediate in heterocyclic synthesis.
2-Cyano-5-hydroxypyridine serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted pyridines and heterocyclic scaffolds. The cyano group facilitates nucleophilic additions and subsequent transformations, while the hydroxyl moiety offers direct derivatization potential via etherification or esterification. Its stability under standard reaction conditions and compatibility with diverse functional groups make it a practical choice for medicinal chemistry lead optimization and process-scale synthesis.
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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: