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Structure of 1073354-07-0
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This boronate ester features a 1,3-dioxolan-2-yl-modified ethyl linker that enhances stability and reactivity in Suzuki-Miyaura coupling. The tetramethyl-substituted dioxaborolane ring provides exceptional bench stability and moisture tolerance. Designed for efficient cross-coupling under standard conditions, it delivers high functional group compatibility and predictable reaction outcomes.
2-(2-(1,3-Dioxolan-2-yl)ethyl)-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 dioxolane-protected aldehyde functionality enables selective transformations under mild conditions, while the tetramethyl-substituted boronate moiety offers excellent functional group tolerance and compatibility with diverse coupling partners. The molecule functions as a versatile synthon in complex molecule assembly, particularly in medicinal chemistry and natural product synthesis 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: