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Structure of 1345091-18-0
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7-Chloro-1,6-naphthyridin-2(1H)-one features a fused bicyclic core with a chlorinated position at C7 and a lactam functionality at N2, offering enhanced electron-withdrawing character. This scaffold integrates readily into pharmaceutical intermediates, enabling efficient access to kinase inhibitors and bioactive heterocycles under standard coupling conditions.
7-Chloro-1,6-naphthyridin-2(1H)-one serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient construction of bioactive scaffolds. Its electrophilic C7-chlorine facilitates palladium-catalyzed cross-coupling reactions, while the 1,6-naphthyridin-2-one core offers hydrogen-bonding capacity and metabolic stability. The compound exhibits bench stability, moderate solubility, and compatibility with common protecting group strategies, making it well-suited for iterative synthesis and lead optimization workflows.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: