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Structure of 1256345-59-1
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(4-Bromo-3-methoxyphenyl)boronic acid features a boronate moiety flanked by a bromine substituent and a methoxy group, enabling selective cross-coupling in palladium-catalyzed reactions. This bench-stable reagent integrates efficiently into complex molecular architectures under standard conditions.
(4-Bromo-3-methoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The bromo and boronic acid functionalities provide orthogonal reactivity for sequential functionalization, while the methoxy group enhances solubility and modulates electronic properties. Bench-stable and readily purified by recrystallization, it facilitates reliable access to substituted biaryls and complex heterocycles in medicinal chemistry and materials synthesis.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: