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Structure of 214360-63-1
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This boronate ester features a methoxy-substituted aryl group enabling efficient cross-coupling in palladium-catalyzed reactions. The tetramethylcyclopentadienone core provides exceptional stability and moisture tolerance, simplifying handling under standard conditions.
2-(4-Methoxy-3-methylphenyl)-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 ortho-methyl and para-methoxy substituents provide predictable regiochemistry and enhanced electronic tuning, enabling efficient C–C bond formation under mild conditions. The tetramethyl-substituted dioxaborolane core ensures excellent shelf stability, low hydrolytic sensitivity, and straightforward purification, making it ideal for iterative synthesis of complex aromatic scaffolds 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 : H302-H312-H332
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: