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Structure of 1706749-51-0
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4-Bromo-2-methyl-2,7-naphthyridin-1(2H)-one features a fused bicyclic core with bromine and methyl substituents enabling diverse functionalization. This electron-deficient heterocycle serves as a key scaffold in kinase inhibitor development and transition-metal-catalyzed coupling reactions. The bench-stable, moisture-tolerant structure facilitates reliable use in synthetic workflows.
4-Bromo-2-methyl-2,7-naphthyridin-1(2H)-one serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C4 position via palladium-catalyzed cross-coupling reactions. The molecule’s stability under standard reaction conditions and compatibility with diverse functional groups facilitate efficient access to substituted naphthyridine scaffolds relevant to kinase inhibitor and antiviral agent development. Its defined regiochemistry and ease of purification make it suitable for scale-up in process-oriented 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 : P260-P264-P270-P271-P280-P301+P310-P302+P352-P304+P340-P305+P351+P338-P312-P330-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: