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Structure of 2446913-88-6
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This dihydropyrimidinone integrates a brominated indazolyl moiety, offering a robust scaffold for medicinal chemistry. The electron-deficient pyrimidinedione core pairs with the sterically accessible bromo-substituted indazole, enabling efficient cross-coupling and diversification. Bench-stable and moisture-tolerant, it streamlines synthesis in target-oriented discovery workflows.
1-(6-Bromo-1-methyl-1H-indazol-3-yl)dihydropyrimidine-2,4(1H,3H)-dione serves as a versatile building block for the synthesis of heterocyclic scaffolds relevant to medicinal chemistry. The bromo group enables palladium-catalyzed cross-coupling reactions, while the dihydropyrimidinone core offers stability and functional group tolerance. Its bench-stable nature and compatibility with standard coupling protocols facilitate efficient access to complex molecular architectures in drug discovery 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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: