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Structure of 1312611-41-8
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This boronate ester features a naphthalene scaffold bearing a tert-butoxycarbonyl-protected amine and a pinacol-stabilized boronic acid group. Designed for late-stage functionalization, it enables efficient Suzuki-Miyaura coupling under mild conditions. The Boc protection ensures stability during storage and handling, while the pinacol moiety enhances solubility and reactivity in aqueous-organic mixtures.
(6-((tert-Butoxycarbonyl)amino)naphthalen-2-yl)boronic acid pinacol ester serves as a stable, bench-ready building block for Suzuki-Miyaura coupling reactions. The Boc-protected amine and pinacol boronate functionalities enable orthogonal reactivity, facilitating sequential transformations in complex molecule synthesis. Its high functional group tolerance and ease of purification make it ideal for constructing naphthalene-based scaffolds in medicinal chemistry and materials science applications.
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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: