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Structure of 1035690-24-4
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This boronate ester integrates a cyclopropoxy-substituted phenyl moiety with a stable tetramethyl-1,3,2-dioxaborolane scaffold. The electron-rich aryl group enables efficient cross-coupling under standard conditions, while the steric protection enhances shelf stability and moisture tolerance. Ideal for Suzuki-Miyaura reactions in complex molecule synthesis.
2-(3-Cyclopropoxyphenyl)-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 cyclopropoxy-substituted aryl group enables efficient C–C bond formation under standard catalytic conditions, with excellent functional group tolerance and predictable regiochemistry. The tetramethyl substituents enhance stability and solubility, facilitating purification and handling in multi-step 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 : 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: