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Structure of 1294009-05-4
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This boronate ester features a propenol side chain that enhances solubility and stability in aqueous media. The tetramethyl-substituted dioxaborolane ring ensures excellent shelf life and resistance to hydrolysis. It integrates readily into Suzuki-Miyaura coupling reactions under mild conditions, enabling efficient C–C bond formation with aryl and vinyl halides.
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)prop-2-en-1-ol serves as a versatile boronate ester building block in palladium-catalyzed cross-coupling reactions. Its vinyl alcohol functionality enables direct incorporation into conjugated systems, while the stabilized dioxaborolane group offers excellent bench stability and compatibility with diverse functional groups. The reagent facilitates efficient Suzuki-Miyaura coupling under mild conditions, enabling rapid assembly of complex molecular architectures with predictable regiochemistry.
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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-H312-H315-H319-H332-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: