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Structure of 49855-91-6
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(S)-2-(((Benzyloxy)carbonyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid serves as a key chiral building block for peptide synthesis, featuring orthogonal protection of both α-amino and side-chain amine functionalities. The benzyloxycarbonyl (Cbz) group at the N-terminus and tert-butoxycarbonyl (Boc) group on the γ-amine enable selective deprotection under distinct conditions, facilitating stepwise assembly of complex peptides. This dipeptide precursor demonstrates excellent stability under standard bench protocols and integrates seamlessly into solid-phase and solution-phase workflows.
(S)-2-(((Benzyloxy)carbonyl)amino)-4-((tert-butoxycarbonyl)amino)butanoic acid serves as a key chiral building block for the synthesis of peptide derivatives and heterocyclic scaffolds. The Boc and Cbz protecting groups enable orthogonal deprotection, facilitating sequential coupling in solid-phase and solution-phase peptide synthesis. Its bench-stable nature and compatibility with standard amine and carboxylic acid transformations make it highly suitable for iterative functionalization in medicinal chemistry 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: