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Structure of 115377-94-1
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This boronic acid features a tert-butoxycarbonyl-protected amine group, enabling selective conjugation in late-stage functionalization. The pendant phenylboronic moiety delivers high reactivity in Suzuki-Miyaura coupling, while the Boc handle ensures stability under standard conditions.
(2-((Tert-butoxycarbonyl)amino)phenyl)boronic acid serves as a stable, bench-ready building block for the synthesis of biaryl scaffolds via Suzuki-Miyaura coupling. The tert-butyl carbamate (Boc) group provides orthogonal protection for the amine, enabling selective functionalization and compatibility with a range of reaction conditions. Its robustness under standard cross-coupling protocols facilitates efficient access to substituted anilines and complex heterocyclic systems relevant to medicinal chemistry and materials science.
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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: