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Structure of 1404480-15-4
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This bench-stable boronic acid derivative features a fused oxazole ring system, enhancing electronic stability and facilitating efficient cross-coupling reactions. The hydrochloride salt improves solubility in aqueous and polar organic media, enabling seamless integration into synthetic workflows requiring precise functional group tolerance and reliable reactivity.
(2-aminobenzo[d]oxazol-5-yl)boronic acid hydrochloride serves as a stable, bench-ready building block for Suzuki-Miyaura coupling reactions. Its ortho-amino and oxazole functionalities enable efficient construction of biologically relevant heterocyclic scaffolds. The hydrochloride salt enhances solubility and handling, while the boronic acid group exhibits robust compatibility with diverse coupling partners, facilitating rapid access to complex molecular architectures in medicinal chemistry and 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-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: