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Structure of 89694-45-1
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This boronic acid features a brominated, methoxy-substituted phenyl core that enables efficient cross-coupling in palladium-catalyzed reactions. The electron-donating methoxy group enhances reactivity while maintaining stability under standard conditions. Ideal for constructing complex aromatic scaffolds in medicinal chemistry and materials synthesis.
(5-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 and electronic tuning for downstream functionalization. Its stability, ease of handling, and compatibility with diverse reaction partners make it well-suited for constructing biaryl scaffolds in medicinal chemistry and materials science applications.
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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 : 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: