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Structure of 710348-42-8
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This boronate moiety integrates seamlessly into Suzuki-Miyaura cross-coupling reactions, delivering high functional group tolerance and stability under standard conditions. The oxazolone scaffold enhances solubility and facilitates orthogonal reactivity in complex molecular architectures.
(2-Oxo-2,3-dihydrobenzo[d]oxazol-5-yl)boronic acid serves as a versatile building block for constructing biologically relevant heterocyclic scaffolds. Its boronic acid functionality enables efficient Suzuki-Miyaura cross-coupling reactions under mild conditions, facilitating the assembly of complex arylated architectures. The oxazolone moiety provides enhanced bench stability and functional group tolerance, simplifying purification and enabling integration into multi-step synthetic sequences common in medicinal chemistry and process development workflows.
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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 : H225
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Precautionary Statements : P210-P233-P240-P241-P242-P243-P280-P370+P378-P501
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Lot numbers can be found on the outside label of a product: