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Structure of 870459-91-9
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This boronate moiety features a chlorine-substituted pyridine ring, enabling direct functionalization in cross-coupling reactions. The electron-deficient heterocycle enhances reactivity in palladium-catalyzed transformations, while the boronic acid group ensures compatibility with standard coupling conditions. Bench-stable and moisture-tolerant, it streamlines synthesis of complex nitrogen-containing scaffolds.
(4-Chloropyridin-2-yl)boronic acid serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki-Miyaura conditions. Its pyridine core provides orthogonal reactivity and enhanced solubility, while the boronic acid moiety offers excellent bench stability and compatibility with diverse functional groups. This reagent facilitates the construction of biaryl scaffolds common in pharmaceutical and agrochemical development.
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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: