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Structure of 1242770-51-9
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(E)-2-(4-Bromostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a bench-stable boronate ester featuring a stereodefined vinyl-boronate linkage. This reagent integrates seamlessly into cross-coupling reactions, enabling efficient access to substituted stilbenes and conjugated systems under mild conditions. The tetramethyl dioxaborolane moiety enhances stability and solubility in organic media.
(E)-2-(4-Bromostyryl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for palladium-catalyzed cross-coupling reactions. It enables efficient Suzuki-Miyaura coupling with aryl halides and triflates, facilitating the construction of biaryl scaffolds under mild conditions. The (E)-configured vinylboronate exhibits high stereoselectivity and functional group tolerance, making it ideal for modular synthesis of complex molecules in medicinal chemistry and materials science applications.
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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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: