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Structure of 165904-29-0
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This boronate ester features a methoxy-substituted propenyl group that enhances reactivity in Suzuki-Miyaura coupling reactions. The tetramethyl-1,3,2-dioxaborolane core provides exceptional stability and moisture tolerance under standard conditions.
2-(3-Methoxyprop-1-en-2-yl)-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 vinyl-bearing structure enables efficient coupling with aryl and heteroaryl halides, while the methoxy group provides modest electronic modulation and enhances solubility. The tetramethyl-substituted dioxaborolane ring ensures excellent shelf stability and compatibility with diverse reaction conditions, facilitating straightforward purification and integration into complex molecule 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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: