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Structure of 1256355-56-2
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This boronic acid features a furan-based scaffold with a hydroxymethyl-functionalized boronate group, enabling direct incorporation into Suzuki-Miyaura cross-coupling reactions. The hydroxymethyl moiety enhances solubility and stability under standard conditions, while the electron-deficient furan ring facilitates efficient coupling with aryl halides.
(5-(Hydroxymethyl)furan-2-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. The pendant hydroxymethyl group provides orthogonal functionality for downstream derivatization, while the boronic acid moiety offers excellent bench stability and compatibility with diverse reaction partners. Its furan core enhances solubility and supports integration into complex heterocyclic scaffolds relevant to 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: