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Structure of 851231-30-6
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This boronate ester features a 2,6-dimethoxyphenyl group attached to a tetramethyl-1,3,2-dioxaborolane scaffold, delivering enhanced stability and solubility in organic solvents. The electron-rich aromatic moiety facilitates efficient coupling in Suzuki-Miyaura reactions, while the steric protection of the dioxaborolane ring minimizes protodeboronation. Ideal for complex molecule synthesis under mild conditions.
2-(2,6-Dimethoxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The 2,6-dimethoxyphenyl group provides enhanced solubility and electronic modulation, while the tetramethyl-substituted dioxaborolane ensures excellent shelf stability and compatibility with diverse reaction conditions. It facilitates efficient C–C bond formation under mild catalytic systems, enabling reliable access to substituted biaryls 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: