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Structure of 248924-59-6
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This boronate ester features a furan-3-yl moiety conjugated to a tetramethyl-substituted dioxaborolane ring, delivering enhanced stability and compatibility with Suzuki-Miyaura cross-coupling reactions. The electron-rich furan system facilitates efficient coupling under mild conditions, while the steric protection of the tetramethyl groups prevents protodeboronation. This combination enables reliable functionalization of aryl halides in complex synthesis workflows.
2-(Furan-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its furan moiety enables efficient incorporation into biaryl and heteroaromatic scaffolds commonly found in pharmaceutical and agrochemical research. The tetramethyl substituents confer excellent thermal stability and resistance to protodeboronation, while facilitating straightforward purification and compatibility with diverse reaction conditions.
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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: