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Structure of 287944-13-2
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This boronate ester features a cycloheptenyl group attached to a stable dioxaborolane ring, enabling efficient cross-coupling reactions under mild conditions. The sterically protected boron center enhances shelf life and resistance to hydrolysis, while the cyclic alkene provides a rigid, electron-rich handle for C–C bond formation in synthetic workflows.
2-(Cyclohept-1-en-1-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 cycloheptenyl moiety enables efficient incorporation into complex carbocyclic scaffolds, with the tetramethyl-substituted dioxaborolane core offering enhanced hydrolytic stability and compatibility with diverse reaction conditions. Ideal for late-stage functionalization and heterocycle construction in medicinal chemistry workflows.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: