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Structure of 216439-76-8
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(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoic acid is a boronate-functionalized amino acid derivative designed for efficient Suzuki-Miyaura cross-coupling reactions. The protected amine and stable boronate handle enable sequential conjugation in peptide and small-molecule synthesis under mild conditions.
(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)propanoic acid serves as a stable, bench-ready building block for Suzuki-Miyaura coupling reactions. The boronate ester group enables efficient C–C bond formation under mild conditions, while the Boc-protected amine and carboxylic acid functionalities offer orthogonal reactivity for peptide and heterocyclic scaffold synthesis. Its high functional group tolerance and ease of purification make it ideal for iterative synthetic workflows 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: