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Structure of 268542-15-0
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BOC-(RS)-3-amino-3-(2-naphthyl)-propionic acid features a sterically hindered chiral center flanked by a naphthyl group and a BOC-protected amine, delivering enhanced stability and ease of handling. This derivative integrates seamlessly into peptide synthesis workflows, enabling efficient access to complex amino acid scaffolds under standard conditions.
BOC-(RS)-3-amino-3-(2-naphthyl)-propionic acid serves as a versatile chiral building block for the synthesis of biologically relevant heterocycles and peptide analogs. The Boc group provides stable protection of the amine under standard conditions, enabling efficient coupling reactions and orthogonal deprotection. Its naphthyl-substituted aliphatic side chain offers enhanced rigidity and lipophilicity, facilitating structural diversity in medicinal chemistry campaigns. The compound exhibits good bench stability and is readily purified by standard chromatographic methods.
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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: