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Structure of 119771-23-2
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(S)-3-(4-Boronophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid features a boronate group enabling efficient Suzuki-Miyaura coupling, paired with a stable tert-butyl carbamate-protected amine. This configuration supports modular peptide and heterocyclic scaffold synthesis under standard conditions.
(S)-3-(4-Boronophenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid serves as a versatile building block for the synthesis of boron-containing amino acids and peptidomimetics. The pendant boronate ester enables facile Suzuki-Miyaura coupling, while the Boc-protected amine and carboxylic acid functionalities offer orthogonal reactivity for peptide elongation and conjugation. Its bench-stable nature and compatibility with standard purification methods make it well-suited for iterative synthetic workflows in medicinal chemistry and target-oriented synthesis.
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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: