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Structure of 90819-30-0
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(S)-2-((tert-Butoxycarbonyl)amino)-3-(3-hydroxyphenyl)propanoic acid features a chiral β-amino acid scaffold with a protected amine and a phenolic hydroxyl group. This configuration enables selective incorporation into peptide sequences, while the ortho-hydroxyaryl moiety supports hydrogen bonding and metal coordination in catalytic or supramolecular systems. The tert-butyl carbamate handle allows for straightforward deprotection under mild acidic conditions, facilitating downstream functionalization.
(S)-2-((tert-Butoxycarbonyl)amino)-3-(3-hydroxyphenyl)propanoic acid serves as a valuable chiral building block for the synthesis of bioactive peptidomimetics and heterocyclic scaffolds. The protected amine enables straightforward N-alkylation or coupling reactions, while the phenolic hydroxyl group supports orthogonal functionalization. Bench-stable and readily purified by chromatography, it functions effectively in standard peptide coupling and cyclization protocols.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: