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Structure of 1403257-80-6
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This brominated benzamide features a sterically hindered pyridone core paired with a tetrahydro-2H-pyran-4-yl amine, delivering enhanced solubility and stability under standard conditions. The ethyl(tetrahydro-2H-pyran-4-yl)amino group enables efficient incorporation into complex molecular architectures, while the 5-bromo substituent provides a reactive handle for downstream functionalization in medicinal chemistry and materials synthesis.
5-Bromo-N-((4,6-dimethyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-3-(ethyl(tetrahydro-2H-pyran-4-yl)amino)-2-methylbenzamide serves as a versatile building block for medicinal chemistry campaigns, enabling efficient access to complex heterocyclic scaffolds. Its bromo group facilitates palladium-catalyzed cross-coupling reactions, while the dihydropyridone core and protected amine functionality offer orthogonal reactivity. The molecule exhibits excellent bench stability, ease of purification, and functional group tolerance, 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-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: