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Structure of 934329-77-8
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This boronate ester integrates a benzofuran-6-yl moiety with a stable tetramethyl-substituted dioxaborolane ring, enabling efficient coupling in Suzuki-Miyaura reactions. The electron-rich heterocycle enhances reactivity while the steric protection ensures shelf stability and moisture tolerance under standard conditions.
2-(Benzofuran-6-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 tetramethyl-substituted dioxaborolane moiety enhances air and moisture stability while enabling efficient coupling with aryl and heteroaryl halides. The benzofuran-6-yl scaffold provides a valuable core for pharmaceutical and agrochemical synthesis, offering compatibility with diverse functional groups and straightforward purification.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: