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Structure of 445303-12-8
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This boronate ester features a 2,3-dihydrobenzofuran scaffold that enhances solubility and stability in aqueous and protic media. The tetramethyl-substituted dioxaborolane ring enables efficient Suzuki-Miyaura coupling under mild conditions, while the fused heterocyclic system imparts unique electronic and steric profiles. Ideal for constructing complex biaryl architectures in medicinal chemistry and materials synthesis.
2-(2,3-Dihydrobenzofuran-6-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its dihydrobenzofuran moiety provides structural relevance to bioactive heterocycles, while the tetramethyl-substituted dioxaborolane enhances stability and functional group tolerance. The compound facilitates efficient C–C bond formation under mild conditions, enabling straightforward access to complex arylated scaffolds 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-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: