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Structure of 55447-00-2
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This chiral building block features a protected (S)-amino acid scaffold with a naphthalen-1-yl substituent, enabling direct incorporation into peptide sequences. The tert-butoxycarbonyl group provides stability and facilitates selective deprotection during synthesis.
(S)-2-((tert-Butoxycarbonyl)amino)-3-(naphthalen-1-yl)propanoic acid serves as a key chiral building block for peptide and heterocyclic synthesis. The Boc-protected amine enables orthogonal functional group manipulation, while the naphthalene moiety provides a rigid aromatic scaffold. This compound exhibits excellent bench stability, facilitates straightforward purification, and participates reliably in standard coupling reactions, making it well-suited for medicinal chemistry campaigns requiring defined stereochemistry and structural complexity.
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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: