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Structure of 652148-91-9
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Lithium hydrogen(5-chloropyridin-2-yl)boronate features a boronate moiety tethered to a chloropyridine ring, enabling direct functionalization in cross-coupling reactions. The electron-deficient pyridine core enhances reactivity in palladium-catalyzed processes, while the bench-stable boronate group facilitates handling under standard conditions. This reagent integrates seamlessly into synthetic sequences requiring selective C–C bond formation.
Lithium hydrogen(5-chloropyridin-2-yl)boronate serves as a versatile boron building block for Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The 5-chloropyridin-2-yl moiety provides a robust platform for further functionalization and is compatible with diverse reaction partners. Its bench-stable nature and high reactivity facilitate reliable synthesis of substituted pyridine derivatives, commonly encountered in pharmaceutical and agrochemical scaffolds.
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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: