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CAS 37439-99-9

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(S)-N-Acetyl-2-naphthylalanine

Description:
(S)-N-Acetyl-2-naphthylalanine is an amino acid derivative characterized by its unique structure, which includes an acetyl group and a naphthalene moiety attached to the amino acid backbone. This compound is a chiral molecule, with the (S) configuration indicating the specific spatial arrangement of its atoms. It is typically used in biochemical research and synthesis, particularly in the study of peptide synthesis and as a building block in the development of pharmaceuticals. The presence of the naphthalene ring contributes to its hydrophobic properties, influencing its solubility and interaction with biological systems. Additionally, the acetyl group enhances its stability and can affect its reactivity. As a compound with potential applications in medicinal chemistry, (S)-N-Acetyl-2-naphthylalanine may exhibit interesting biological activities, making it a subject of interest in drug design and development. Proper handling and storage are essential due to its chemical properties, and it should be used in accordance with safety guidelines in laboratory settings.
Formula:C15H15NO3
InChI:InChI=1/C15H15NO3/c1-10(17)16-14(15(18)19)9-11-6-7-12-4-2-3-5-13(12)8-11/h2-8,14H,9H2,1H3,(H,16,17)(H,18,19)/t14-/m0/s1
SMILES:CC(=N[C@@H](Cc1ccc2ccccc2c1)C(=O)O)O
Synonyms:
  • (2S)-2-(acetylamino)-3-naphthalen-2-ylpropanoic acid (non-preferred name)
  • (S)-N-ACETYL-2-NAPHTHYLALANINE
  • N-Acetyl-3-(2-naphthyl)-L-alanine
  • N-Acetyl-3-naphth-2-yl-L-alanine
  • (S)-N-Acetyl-2-naphthylalanine USP/EP/BP
  • (2S)-2-acetamido-3-(naphthalen-2-yl)propanoic acid
  • (S)-2-ACETAMIDO-3-(NAPHTHALEN-2-YL) PROPANOIC ACID
  • (2S)-2-(Acetylamino)-3-(naphth-2-yl)propanoic acid
  • (S)-N-Acetyl-2-naphthylalanine &nbsp
  • (S)-N-ACETYL-2-NAPHTHYLALANINE /NOBR>
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