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Structure of 171364-84-4
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This boronate ester features a sterically shielded dioxaborolane ring paired with an electron-rich aryl group, delivering enhanced stability and reactivity in cross-coupling processes. Designed for robust performance under standard conditions, it enables efficient C–C bond formation in synthetic workflows.
4,4,5,5-Tetramethyl-2-(2,4,6-trimethylphenyl)-1,3,2-dioxaborolane serves as a stable, bench-ready boron reagent enabling efficient Suzuki-Miyaura cross-coupling reactions. Its sterically protected dioxaborolane core enhances shelf life and minimizes protodeboronation, while the electron-rich aryl group facilitates rapid transmetalation. The compound exhibits broad functional group tolerance and simplifies purification due to low byproduct formation, making it ideal for constructing complex biaryls and heterocyclic scaffolds in medicinal chemistry and materials synthesis workflows.
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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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: