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Structure of 325142-93-6
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This boronate ester features a sterically shielded tetramethyl-1,3,2-dioxaborolane ring paired with a 3,5-dimethylphenyl substituent, delivering enhanced stability and reactivity in Suzuki-Miyaura cross-coupling. The electron-rich aryl group facilitates efficient palladium-catalyzed bond formation under standard conditions.
2-(3,5-Dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its ortho-substituted aryl group enhances regioselectivity in coupling processes, while the tetramethyl-substituted dioxaborolane core provides excellent stability and compatibility with diverse reaction conditions. The compound facilitates efficient C–C bond formation under mild catalytic conditions, enabling reliable access to biaryl scaffolds in medicinal chemistry and materials synthesis.
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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
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Lot numbers can be found on the outside label of a product: