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Structure of 500770-69-4
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This chiral building block features a protected (S)-amino acid scaffold bearing a naphthalen-2-yl group at the beta position, enabling direct incorporation into peptide-based scaffolds. The tert-butoxycarbonyl (Boc) group provides orthogonal protection for amine functionality under standard coupling conditions, while the rigid naphthalene moiety imparts enhanced structural definition and potential for π–π interactions in target-directed synthesis.
(S)-3-((tert-Butoxycarbonyl)amino)-3-(naphthalen-2-yl)propanoic acid serves as a chiral building block for the synthesis of bioactive molecules, leveraging its pendant naphthalene moiety and protected amino group. The Boc-protected amine enables straightforward deprotection and coupling reactions, while the α-amino acid scaffold facilitates incorporation into peptide-like architectures. Its bench-stable solid form and compatibility with standard peptide coupling protocols make it suitable for medicinal chemistry campaigns requiring stereocontrolled access to complex heterocyclic and fused-ring systems.
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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: