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Structure of 153724-93-7
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(E)-2-(3-Chloroprop-1-en-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for palladium-catalyzed cross-coupling reactions. Its (E)-configured vinyl boronate enables stereoselective incorporation into conjugated systems, while the tetramethyl-substituted dioxaborolane enhances stability and functional group tolerance. The molecule facilitates efficient coupling with aryl, heteroaryl, and vinyl halides, offering reliable access to functionalized alkenes in synthetic and medicinal chemistry workflows.
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Lot numbers can be found on the outside label of a product: