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Structure of 250611-08-6
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(S)-tert-Butyl 4-amino-2-((tert-butoxycarbonyl)amino)butanoate hydrochloride features a chiral backbone with orthogonal protection, enabling selective deprotection during peptide synthesis. The tert-butyl carbamate group offers stability under basic conditions, while the primary amine facilitates efficient coupling reactions. This bench-stable derivative streamlines access to complex amino acid analogs in medicinal chemistry workflows.
(S)-tert-Butyl 4-amino-2-((tert-butoxycarbonyl)amino)butanoate hydrochloride serves as a key chiral building block for the synthesis of peptidomimetics and bioactive heterocycles. The protected amine and amino acid backbone enable straightforward functionalization, while the tert-butyl carbamate group offers stability and orthogonal deprotection. Its bench-stable hydrochloride salt facilitates handling and purification in standard synthetic 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: