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Structure of 889849-21-2
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This boronic acid features a brominated, methoxy-substituted phenyl core that enables efficient coupling in palladium-catalyzed reactions. The electron-donating methoxy group enhances reactivity while maintaining stability under standard conditions. This bench-stable reagent integrates readily into complex molecular architectures during late-stage functionalization workflows.
(4-Bromo-2-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 methoxy groups provide orthogonal reactivity for sequential functionalization, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction substrates. Its predictable coupling behavior and straightforward purification make it a reliable choice for constructing complex aryl scaffolds 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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: