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Structure of 945756-49-0
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This boronate reagent features a tert-butoxycarbonyl-protected amine and a phenylboronic acid handle, enabling orthogonal functionalization in synthetic sequences. The protected amine allows for selective deprotection post-coupling, while the boronic acid group facilitates palladium-catalyzed cross-couplings under mild conditions. Designed for streamlined access to complex arylamine architectures, it offers bench-stable handling and compatibility with diverse reaction media.
(4-((Tert-butoxycarbonyl)(methyl)amino)phenyl)boronic acid serves as a versatile building block for Suzuki-Miyaura coupling reactions, enabling the construction of biaryl scaffolds under mild conditions. The tert-butoxycarbonyl (Boc) group provides orthogonal protection for the amine functionality, allowing selective deprotection in subsequent steps. Its stability, ease of handling, and compatibility with diverse reaction partners make it well-suited for applications 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-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: