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Structure of 1227068-84-9
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This boronate ester features a difluorocyclohexenyl moiety that enhances metabolic stability and modulates electronic properties. The tetramethyl-substituted dioxaborolane ring ensures excellent shelf life and moisture tolerance, enabling reliable use in Suzuki-Miyaura cross-coupling reactions under standard conditions.
2-(4,4-Difluorocyclohex-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for palladium-catalyzed cross-coupling reactions. Its difluorocyclohexenyl moiety enables efficient incorporation into bioactive scaffolds, while the tetramethyl-substituted dioxaborolane core ensures high chemical stability and compatibility with diverse reaction conditions. Facilitates reliable C–C bond formation in medicinal chemistry and materials synthesis workflows.
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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: