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Structure of 888721-86-6
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This morpholine-substituted pyridylboronate integrates readily into cross-coupling reactions, offering robust stability under standard conditions. The tetramethyl-1,3,2-dioxaborolane moiety enables efficient palladium-catalyzed transformations, while the electron-rich morpholine ring enhances solubility and reactivity in diverse synthetic environments.
4-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl)morpholine serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyridine-2-yl moiety enables efficient coupling with aryl and heteroaryl halides, while the morpholine ring provides solubility and favorable electronic properties. Bench-stable and compatible with diverse functional groups, it facilitates rapid assembly of complex scaffolds in medicinal chemistry and materials science 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: