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Structure of 754226-40-9
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This boronate ester integrates a benzyloxy-substituted phenyl moiety with a stable tetramethyl-1,3,2-dioxaborolane ring, enabling efficient Suzuki-Miyaura coupling under standard conditions. The benzyl protecting group ensures excellent shelf stability and compatibility with diverse reaction environments.
2-(4-(Benzyloxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-friendly boronate building block for Suzuki-Miyaura cross-coupling reactions. The benzyloxy group provides orthogonal protection and enhances solubility, while the tetramethyl-substituted dioxaborolane core ensures excellent shelf stability and compatibility with diverse reaction conditions. It facilitates efficient C–C bond formation in complex molecule synthesis, particularly in medicinal chemistry and natural product derivatization 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-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: