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Structure of 1242314-44-8
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This boronate moiety features a brominated pyridine core with a methoxy group at the 2-position, enabling selective cross-coupling reactions. The pendant boronic acid group delivers high reactivity in Suzuki-Miyaura transformations under standard conditions. This bench-stable compound integrates readily into complex molecular architectures requiring halogen-directed functionalization and exhibits excellent compatibility with diverse reaction partners.
(6-Bromo-2-methoxypyridin-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 bromine and boronic acid functionalities offer orthogonal reactivity for sequential functionalization, while the methoxy group enhances solubility and modulates electronic properties. Its bench-stable nature and compatibility with standard Suzuki-Miyaura conditions make it ideal for medicinal chemistry and process development 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: