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Structure of 81306-93-6
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(R)-3-(((Benzyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)propanoic acid is a chiral dipeptide precursor featuring orthogonal protection of both α-amino groups. The benzyloxycarbonyl (Boc) and tert-butoxycarbonyl (Boc) moieties enable sequential deprotection during peptide synthesis, facilitating efficient coupling and purification. This bench-stable derivative supports the construction of complex peptide architectures with high fidelity.
(R)-3-(((Benzyloxy)carbonyl)amino)-2-((tert-butoxycarbonyl)amino)propanoic acid serves as a key chiral building block for peptide synthesis, enabling efficient access to protected dipeptide intermediates. The orthogonal protection of both α-amino groups—benzyloxycarbonyl (Cbz) and tert-butoxycarbonyl (Boc)—facilitates sequential coupling strategies. Its bench-stable solid form and compatibility with standard deprotection protocols streamline workflow integration in medicinal chemistry and process development.
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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: