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Structure of 459856-12-3
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions, delivering functionalized heteroaryl products with high efficiency. The methoxy and methyl substituents enhance solubility and stability under standard conditions, enabling straightforward handling in synthetic workflows.
(6-Methoxy-2-methylpyridin-3-yl)boronic acid serves as a versatile building block in palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. The methoxy and methyl groups provide orthogonal functional handles for further derivatization, while the boronic acid moiety exhibits excellent bench stability and compatibility with diverse reaction conditions. Its predictable reactivity and ease of purification make it a practical choice for medicinal chemistry and process development workflows.
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GHS No : GHS05
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Signal Word : Danger
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UN#: 3261
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H315-H318-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: