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Structure of 902148-83-8
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This boronate moiety integrates readily into Suzuki-Miyaura couplings, delivering pyridine-based scaffolds with high functional group tolerance. The electron-deficient pyridine ring enhances reactivity in cross-coupling processes, while the pendant ketone enables downstream derivatization. Bench-stable and moisture-tolerant, it simplifies handling in synthetic workflows.
(2-Oxo-1,2-dihydropyridin-4-yl)boronic acid serves as a versatile building block for the synthesis of pyridine-containing scaffolds, enabling direct Suzuki-Miyaura coupling reactions under mild conditions. Its boronic acid functionality offers excellent bench stability and compatibility with diverse functional groups, facilitating efficient access to medicinally relevant heterocycles and advanced intermediates in small-molecule 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-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: