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CAS 1186216-21-6

:

FMoc-(S)-3-AMino-4-(2-naphthyl)-butyric acid

Description:
FMoc-(S)-3-Amino-4-(2-naphthyl)-butyric acid is a chemical compound characterized by its structure, which includes a fluorenylmethyloxycarbonyl (FMoc) protecting group attached to an amino acid backbone. This compound features a chiral center at the 3-position, contributing to its stereochemical properties, specifically the (S) configuration. The presence of a 2-naphthyl group enhances its hydrophobic characteristics, making it useful in various biochemical applications, particularly in peptide synthesis and drug development. The FMoc group serves as a protective moiety for the amino group, allowing for selective reactions during synthesis. This compound is typically utilized in the field of medicinal chemistry and peptide research, where the manipulation of amino acids is crucial for developing bioactive molecules. Its unique structural features may also influence its solubility, reactivity, and interaction with biological targets, making it a valuable compound in the study of pharmacological properties and the design of therapeutic agents.
Formula:C29H25NO4
Synonyms:
  • (S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(naphthalen-2-yl)butanoic acid
  • N-β-(9-Fluorenylmethoxycarbonyl)-γ-(2-naphthyl)-L-β-homoalanine
  • (9H-Fluoren-9-yl)MethOxy]Carbonyl (S)-3-Amino-4-(2-naphthyl)-butyric acid
  • (3S)-3-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)-4-(naphthalen-2-yl)butanoic acid
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