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Structure of 352525-80-5
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(3-Bromo-2-methoxyphenyl)boronic acid features a boronate moiety flanked by a bromine atom and a methoxy group, enabling selective cross-coupling in palladium-catalyzed reactions. The electron-rich aromatic core enhances reactivity, while the methoxy substituent improves solubility and stability under standard conditions.
(3-Bromo-2-methoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. Its stability, ease of handling, and compatibility with diverse functional groups make it ideal for constructing biaryl scaffolds in medicinal chemistry and materials science. The bromo and methoxy substituents provide orthogonal reactivity and electronic tuning for downstream modifications.
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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: