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Structure of 1394003-98-5
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6-Chloro-1,5-naphthyridin-2(1H)-one features a chlorine-substituted naphthyridinone core with enhanced electron-deficiency, enabling efficient coupling in transition-metal-catalyzed reactions. This bench-stable heterocycle serves as a key scaffold for medicinal chemistry and materials synthesis, offering high functional group tolerance and predictable reactivity in cross-coupling protocols.
6-Chloro-1,5-naphthyridin-2(1H)-one serves as a versatile heterocyclic building block in medicinal chemistry, enabling efficient functionalization via palladium-catalyzed cross-coupling reactions. Its chlorine atom provides high reactivity in Suzuki, Stille, and Buchwald-Hartwig transformations, while the adjacent carbonyl group enhances solubility and facilitates downstream derivatization. The scaffold exhibits excellent bench stability and compatibility with diverse functional groups, making it ideal for rapid library synthesis and API development.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: