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Structure of 1562375-30-7
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tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enecarboxylate features a boronate ester group integrated into a cyclohexenyl framework, enabling efficient Suzuki-Miyaura cross-coupling reactions. The tetramethyl-substituted dioxaborolane moiety ensures high stability and reactivity under standard conditions. This bench-stable reagent facilitates the direct introduction of functionalized cyclohexenyl units into complex molecular architectures.
tert-Butyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enecarboxylate serves as a stable, bench-ready boron building block for palladium-catalyzed cross-coupling reactions. The cyclohexenyl scaffold enables efficient access to substituted dienes and conjugated systems, while the tert-butyl ester offers orthogonal protection and facile downstream modification. Its high functional group tolerance and compatibility with standard Suzuki-Miyaura conditions make it ideal for iterative synthesis of complex molecular architectures in medicinal chemistry and materials science.
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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
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: