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Structure of 685514-61-8
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This boronate moiety integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions, delivering biaryl architectures with high functional group tolerance. The dihydrobenzofuran scaffold provides a rigid, electron-rich platform ideal for medicinal chemistry applications.
(2,3-Dihydrobenzofuran-7-yl)boronic acid serves as a versatile building block in Suzuki-Miyaura cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its stable boronic acid functionality exhibits good bench stability and compatibility with diverse functional groups, facilitating the synthesis of biaryl architectures found in pharmaceutical intermediates and agrochemical scaffolds. The dihydrobenzofuran core provides structural rigidity and lipophilic character beneficial for modulating compound properties in medicinal chemistry 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 : 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: