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Structure of 261621-12-9
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This boronate moiety features a silyl-protected phenolic oxygen, enabling stable handling and selective deprotection during late-stage functionalization. The tert-butyldimethylsilyl group imparts enhanced solubility and moisture tolerance, while the boronic acid functionality facilitates efficient Suzuki-Miyaura coupling under standard conditions.
(3-((Tert-butyldimethylsilyl)oxy)phenyl)boronic acid serves as a stable, bench-ready building block for Suzuki-Miyaura coupling reactions. The silyl ether group provides orthogonal protection for phenolic hydroxyls, enabling selective functionalization in complex molecule synthesis. Its robustness under standard reaction conditions and compatibility with diverse coupling partners facilitate efficient construction of biaryl architectures in medicinal chemistry and materials science workflows.
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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-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: