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Structure of 219297-11-7
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(S)-3-((tert-Butoxycarbonyl)amino)-4-(naphthalen-2-yl)butanoic acid features a chiral center at the 3-position, bearing a tert-butoxycarbonyl-protected amine and a naphthalen-2-yl group at the 4-position. This configuration enables direct incorporation into peptide synthesis workflows, where the Boc group facilitates selective deprotection under mild acidic conditions. The extended aromatic system enhances rigidity and hydrophobic character, beneficial for stabilizing secondary structures in bioactive peptides.
(S)-3-((tert-Butoxycarbonyl)amino)-4-(naphthalen-2-yl)butanoic acid serves as a stable, bench-ready chiral building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The protected amine and carboxylic acid functionalities enable orthogonal transformations in multi-step sequences. Its naphthalene moiety provides a rigid, hydrophobic core useful in medicinal chemistry campaigns targeting protein-protein interactions.
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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-H312-H332
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
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Lot numbers can be found on the outside label of a product: