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Structure of 1256358-90-3
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This boronate-functionalized pyridinone integrates readily into Suzuki-Miyaura coupling reactions under mild conditions. The tetramethylborolane moiety enhances stability and solubility, while the electron-deficient pyridinone ring enables selective functionalization in complex molecular scaffolds.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2(1H)-one serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. Its pyridin-2-one core provides enhanced stability and solubility compared to analogous heterocycles, while the tetramethylboronate moiety enables efficient coupling under mild conditions. The compound exhibits excellent functional group tolerance and bench stability, facilitating reliable incorporation into complex molecular architectures common in medicinal chemistry and materials science applications.
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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: