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Structure of 796851-30-4
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This boronate ester integrates a benzofuran-3-yl moiety with a sterically shielded tetramethyl-1,3,2-dioxaborolane group, delivering enhanced stability and compatibility in Suzuki-Miyaura coupling reactions. The electron-rich aromatic system facilitates efficient palladium-catalyzed cross-coupling under standard conditions, enabling rapid access to biaryl architectures in medicinal chemistry and materials synthesis.
2-(Benzofuran-3-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 tetramethyl-substituted dioxaborolane moiety enhances air and moisture stability while enabling efficient coupling with aryl and heteroaryl halides. The benzofuran scaffold provides a versatile core for constructing biologically relevant molecules and functional materials, with excellent functional group tolerance and straightforward purification via flash chromatography.
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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 : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: