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Structure of 38767-72-5
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4-Aminopyridin-2(1H)-one features a fused pyridone core with a strategically positioned amino group, enabling strong hydrogen bonding and enhanced solubility. This scaffold integrates readily into bioactive molecules, serving as a key pharmacophore in kinase inhibitors and antiviral agents. The compound exhibits robust stability under standard bench conditions and facilitates efficient derivatization via amine functionalization.
4-Aminopyridin-2(1H)-one serves as a versatile scaffold in medicinal chemistry, enabling rapid access to diverse heterocyclic systems through its dual functionality: a nucleophilic amine and a hydrogen-bond-capable carbonyl. It functions as a key building block in the synthesis of kinase inhibitors and other bioactive molecules, offering excellent bench stability, straightforward purification, and compatibility with standard coupling and cyclization protocols.
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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: