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Structure of 444094-88-6
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This boronate ester features a 4-chlorophenethyl group attached to a stable tetramethyl-1,3,2-dioxaborolane core. It integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, offering reliable performance with minimal decomposition. The electron-deficient aryl chloride moiety enhances reactivity in palladium-catalyzed transformations.
2-(4-Chlorophenethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-friendly boron building block for Suzuki-Miyaura cross-coupling reactions. The chlorophenethyl moiety enables direct functionalization of aromatic systems with high chemoselectivity and excellent tolerance to diverse reaction conditions. Its tetramethyl-substituted dioxaborolane core ensures low hydrolytic sensitivity and ease of purification, making it ideal 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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
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Lot numbers can be found on the outside label of a product: