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Structure of 1351413-50-7
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering stable, high-yielding transformations under standard conditions. The dihydropyridone scaffold enhances solubility and electronic tuning, enabling efficient functionalization of complex heterocycles in synthetic medicinal chemistry workflows.
(1-Methyl-2-oxo-1,2-dihydropyridin-4-yl)boronic acid serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions with aryl and heteroaryl halides. Its stability under ambient conditions and compatibility with diverse functional groups facilitate efficient synthesis of pyridinone-containing scaffolds. The boronic acid moiety provides reliable coupling efficiency and ease of purification, making it well-suited for iterative library construction and lead optimization workflows.
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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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: