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Catalog Number:
29687
CAS Number:
1820571-03-6
Acide 2 S ,4 R -Fmoc-4-cyclohexyl-pyrrolidine-2-carboxylique
Purity:
≥ 99 % (HPLC)
Documents
$127.79 /25 mg
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Informations sur le produit

The compound (2S,4R)-Fmoc-4-cyclohexyl-pyrrolidine-2-carboxylic acid is a valuable building block in peptide synthesis, particularly in the development of pharmaceuticals and biologically active compounds. Its unique structure, featuring a cyclohexyl group, enhances the compound's hydrophobic properties, making it an excellent choice for improving the solubility and stability of peptides. This compound is widely utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of various peptide-based drugs. Researchers appreciate its ability to facilitate the formation of complex structures while maintaining high yields and purity.

Moreover, the Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy deprotection under mild conditions, making it a preferred choice for chemists looking to streamline their synthetic processes. Its application extends to the development of novel therapeutics, including those targeting specific diseases, where precise control over peptide structure is crucial. With its advantageous properties and practical applications, (2S,4R)-Fmoc-4-cyclohexyl-pyrrolidine-2-carboxylic acid stands out as a significant compound for researchers and industry professionals alike.

Numéro CAS 
1820571-03-6
Formule moléculaire
C 26 H 294
Poids moléculaire 
419.52
Rotation optique 
[a] D 20 = -56 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
1820571-03-6
Formule moléculaire
C 26 H 294
Poids moléculaire 
419.52
Rotation optique 
[a] D 20 = -56 ± 2º (C = 1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
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Applications

(2S,4R)-Fmoc-4-cyclohexyl-pyrrolidine-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions and enhancing the efficiency of the process.
  • Drug Development: Its structural properties make it valuable in the design of new pharmaceuticals, particularly in creating compounds with improved bioavailability and stability.
  • Bioconjugation: It is used in attaching biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: The compound's unique structure can be utilized in studies related to neuroactive peptides, potentially leading to advances in treatments for neurological disorders.
  • Material Science: Its properties can be leveraged in the creation of novel materials, such as polymers with specific mechanical or thermal characteristics.

Citations