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Structure of 1581771-55-2
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This boronate ester features a methoxyethyl side chain that enhances solubility in polar solvents while maintaining stability under standard handling conditions. The tetramethyl-substituted dioxaborolane ring provides excellent shelf life and resistance to hydrolysis, enabling reliable use in Suzuki-Miyaura coupling reactions.
2-(2-Methoxyethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane serves as a stable, bench-ready boron building block for Suzuki-Miyaura cross-coupling reactions. Its tetramethyl-substituted dioxaborolane core enhances shelf stability and functional group tolerance, while the 2-methoxyethyl side chain provides orthogonal handle for further derivatization. The compound facilitates efficient C–C bond formation under mild conditions, enabling rapid access to complex aryl- and heteroaryl-containing scaffolds in medicinal chemistry and materials synthesis.
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GHS Pictogram :
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GHS No : GHS05,GHS07
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Signal Word : Danger
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UN#: 1993
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Class : 3
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Packing Group : Ⅱ
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Hazard Statements : H225-H315-H319-H335
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Precautionary Statements : P210-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P362-P370+P378-P403+P233-P403+P235-P405-P501
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Lot numbers can be found on the outside label of a product: