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Structure of 951655-49-5
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This boronate moiety integrates a pyridine-based scaffold with enhanced stability and solubility. It enables direct coupling in Suzuki-Miyaura reactions under mild conditions, offering reliable performance in complex molecule assembly. The electron-deficient heterocycle facilitates selective transformations while maintaining bench-stable handling properties.
(2-Oxo-1,2-dihydropyridin-3-yl)boronic acid serves as a versatile building block for the synthesis of pyridine-based heterocycles and bioactive scaffolds. Its boronic acid functionality enables efficient Suzuki-Miyaura coupling reactions under mild conditions, while the adjacent ketone group provides orthogonal reactivity for downstream transformations. The compound exhibits good bench stability and is compatible with diverse functional groups, facilitating streamlined access to complex molecular architectures in medicinal chemistry and process R&D 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-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: