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Structure of 1443987-72-1
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This boronate moiety integrates a sterically protected, bench-stable dihydrobenzimidazolone scaffold, enabling efficient coupling in Suzuki-Miyaura reactions. The electron-deficient arylboronic acid features enhanced stability and predictable reactivity under standard conditions.
(1,3-Dimethyl-2-oxo-2,3-dihydro-1H-benzo[d]imidazol-5-yl)boronic acid serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. Its stable boronic acid functionality enables efficient C–C bond formation with aryl and heteroaryl halides under mild conditions. The benzoimidazolone core provides enhanced bench stability and favorable solubility, facilitating straightforward purification and integration into complex molecular architectures relevant to medicinal chemistry and functional materials synthesis.
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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
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Precautionary Statements : P264-P270-P280-P302+P352-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: