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Structure of 710348-69-9
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This boronate-functionalized benzoimidazolone integrates readily into Suzuki-Miyaura coupling reactions under standard conditions. The tetramethylboronate moiety enhances stability and solubility, enabling efficient cross-coupling with aryl halides. This bench-stable reagent streamlines the synthesis of biaryl-linked heterocycles for medicinal chemistry applications.
5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3-dihydro-2H-benzo[d]imidazol-2-one serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The stable boronate ester group enables efficient C–C bond formation under mild conditions, while the benzo[d]imidazol-2-one scaffold provides a rigid, electron-deficient heterocyclic core with favorable solubility and bench stability. Functions reliably in diverse synthetic workflows, including late-stage functionalization and library synthesis.
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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: