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Structure of 7148-78-9
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This boronate ester features a stable, bench-ready ethoxy-substituted enol ether linkage that enables efficient cross-coupling under mild conditions. The para-aryl group enhances electronic stability while the diethoxypropenyl motif delivers high reactivity in Suzuki-Miyaura transformations without requiring specialized handling.
(3,3-Diethoxyprop-1-en-1-yl)benzene serves as a versatile synthetic building block for constructing functionalized allylic systems and heterocyclic scaffolds. Its enol ether functionality enables controlled electrophilic transformations and participates in palladium-catalyzed coupling reactions with high chemoselectivity. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative synthesis workflows in medicinal chemistry and process development.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: