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Structure of 68716-52-9
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This boronate ester integrates a naphthalen-1-yl group with a sterically shielded tetramethylcyclopentadienone core, enabling stable coupling in Suzuki-Miyaura reactions. The electron-rich aryl moiety enhances reactivity under standard conditions, while the hindered substituents confer robustness to hydrolysis and air exposure.
4,4,5,5-Tetramethyl-2-(naphthalen-1-yl)-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. Its naphthyl moiety enables efficient incorporation into extended π-systems and heterocyclic scaffolds. The tetramethyl-substituted dioxaborolane offers enhanced stability and mild reaction conditions, facilitating functional group tolerance and straightforward purification—ideal for iterative synthesis in medicinal chemistry and materials science 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 : H315-H319-H335
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Precautionary Statements : P233-P260-P261-P264-P271-P280-P302+P352-P304+P340-P340-P362-P403-P405-P501
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Lot numbers can be found on the outside label of a product: