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Structure of 652148-90-8
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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 processes, delivering diverse N-heteroaryl architectures under standard conditions.
(6-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 chlorine substituent provides orthogonal reactivity for downstream functionalization, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction partners. This compound facilitates the construction of biaryl scaffolds and complex heterocyclic systems commonly found in pharmaceutical intermediates and agrochemicals.
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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 : H315-H319-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: