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Structure of 65710-57-8
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(S)-3-Benzyloxycarbonylamino-2-(Boc-amino)propionic acid features a chiral backbone with orthogonal protecting groups: a benzyl ester at the C-terminal carboxylate and a tert-butoxycarbonyl group on the side-chain amine. This dual protection enables selective deprotection during peptide synthesis, streamlining access to functionalized amino acid intermediates. The molecule exhibits excellent stability under standard bench conditions and facilitates efficient coupling reactions in solid-phase and solution-phase workflows.
(S)-3-Benzyloxycarbonylamino-2-(Boc-amino)propionic acid serves as a key chiral building block for the synthesis of peptide mimetics and β-amino acid derivatives. Its dual protected amine functionality—benzyloxycarbonyl (Cbz) at the α-position and tert-butoxycarbonyl (Boc) at the side chain—enables orthogonal deprotection sequences in complex peptide assembly. The molecule exhibits excellent bench stability, facilitates straightforward purification, and participates reliably in standard coupling reactions, making it a practical choice for solid-phase and solution-phase peptide synthesis workflows.
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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: