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Structure of 259209-17-1
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This boronic acid features a hydroxyl and methoxy group ortho to the boronate, enhancing solubility and stability. The phenolic OH enables hydrogen bonding and facilitates coupling reactions under mild conditions. Designed for efficient Suzuki-Miyaura cross-coupling in complex molecule synthesis, this reagent combines predictable reactivity with bench-stable handling.
(2-Hydroxy-3-methoxyphenyl)boronic acid serves as a versatile building block in Suzuki-Miyaura coupling reactions, enabling efficient construction of biaryl and heteroaryl architectures. Its ortho-hydroxyl and methoxy substituents provide enhanced solubility and stability compared to unsubstituted analogs, while maintaining compatibility with standard reaction conditions. The molecule facilitates direct functionalization of complex scaffolds and supports iterative synthesis workflows in medicinal chemistry and materials science.
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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: