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Structure of 214360-76-6
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This boronate ester features a hydroxylated phenylboronate moiety, offering enhanced stability and solubility in aqueous-organic mixtures. It functions as a key coupling partner in Suzuki-Miyaura reactions, enabling efficient C–C bond formation under mild conditions. The pinacol protection group confers bench-stability and tolerance to moisture, streamlining handling in synthetic workflows.
3-Hydroxyphenylboronic acid pinacol ester serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its pinacol ester functionality enhances air and moisture stability while enabling selective activation under mild basic conditions. The ortho-hydroxyl group provides additional coordination potential and facilitates downstream functionalization in heterocyclic synthesis, making it valuable for constructing complex phenolic scaffolds 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 : 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: