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CAS 268542-15-0

:

3-[(tert-butoxycarbonyl)amino]-3-naphthalen-2-ylpropanoic acid

Description:
3-[(tert-butoxycarbonyl)amino]-3-naphthalen-2-ylpropanoic acid, with the CAS number 268542-15-0, is an organic compound characterized by its complex structure that includes a naphthalene moiety and a tert-butoxycarbonyl (Boc) protecting group. This compound features an amino acid backbone, which contributes to its potential applications in peptide synthesis and medicinal chemistry. The presence of the naphthalene ring imparts hydrophobic characteristics, while the carboxylic acid functional group provides acidic properties, making it soluble in polar solvents. The Boc group serves as a protective group for the amino functionality, allowing for selective reactions during synthetic processes. This compound is typically utilized in the synthesis of more complex molecules, particularly in the development of pharmaceuticals. Its stability and reactivity can be influenced by the surrounding functional groups, making it a versatile intermediate in organic synthesis. Overall, this compound exemplifies the intersection of organic chemistry and medicinal applications, showcasing the importance of functional group manipulation in drug design.
Formula:C18H21NO4
InChI:InChI=1/C18H21NO4/c1-18(2,3)23-17(22)19-15(11-16(20)21)14-9-8-12-6-4-5-7-13(12)10-14/h4-10,15H,11H2,1-3H3,(H,19,22)(H,20,21)
SMILES:CC(C)(C)OC(=NC(CC(=O)O)c1ccc2ccccc2c1)O
Synonyms:
  • 2-Naphthalenepropanoic Acid, Beta-[[(1,1-Dimethylethoxy)Carbonyl]Amino]-
  • 3-[(tert-Butoxycarbonyl)amino]-3-(2-naphthyl)propanoic acid
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