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Structure of 1310384-20-3
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4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enecarbonitrile features a boronate ester group paired with an electron-deficient alkene and nitrile functionality, enabling efficient palladium-catalyzed cross-coupling reactions. This bench-stable reagent integrates seamlessly into complex molecule assembly workflows, particularly in the synthesis of conjugated systems and functionalized cyclohexenones.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enecarbonitrile serves as a versatile boron-containing building block for Suzuki-Miyaura cross-coupling reactions. The stable pinacol boronate ester enables efficient C–C bond formation under mild conditions, while the conjugated enecarbonitrile moiety provides a rigid, electron-deficient scaffold suitable for constructing functionalized heterocycles and pharmaceutical intermediates. Bench-stable and compatible with diverse reaction conditions, it facilitates rapid access to complex molecular architectures in medicinal chemistry and materials science applications.
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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: