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Catalog Number:
04940
CAS Number:
204321-85-7
Acide Fmoc-(2 S ,4 S -4-amino-1-benzoyl-pyrrolidine-2-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-AZPC( 2S , 4S- OH)
Documents
$65.40 /100 mg
Taille
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Informations sur le produit

Fmoc-(2S,4S)-4-amino-1-benzoyl-pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique Fmoc (9-fluorenylmethoxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structural attributes, including the benzoyl and pyrrolidine moieties, enhance its stability and reactivity, making it an ideal candidate for various applications in drug development and biochemistry. Researchers appreciate its ability to facilitate the formation of complex peptide sequences, which are crucial in the design of therapeutic agents and biologically active compounds.

In addition to its role in peptide synthesis, Fmoc-(2S,4S)-4-amino-1-benzoyl-pyrrolidine-2-carboxylic acid is also valuable in the development of novel materials and bioactive molecules. Its unique properties allow for the exploration of new pathways in drug discovery, particularly in the field of targeted therapies. By incorporating this compound into their research, professionals can streamline their synthesis processes and enhance the efficacy of their compounds, ultimately leading to innovative solutions in pharmaceuticals and biotechnology.

Numéro CAS 
204321-85-7
Formule moléculaire
C27H24N2O5
Poids moléculaire 
456.5
Rotation optique 
[a] D 20
Informations générales
Numéro CAS 
204321-85-7
Formule moléculaire
C27H24N2O5
Poids moléculaire 
456.5
Rotation optique 
[a] D 20
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-(2S,4S)-4-amino-1-benzoyl-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without affecting other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: It is employed in the synthesis of neuropeptides, aiding researchers in studying neurological pathways and developing treatments for neurodegenerative diseases.
  • Analytical Chemistry: This chemical is utilized in the development of analytical methods for peptide characterization, providing researchers with tools to assess purity and structure effectively.

Citations