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Catalog Number:
02388
CAS Number:
118534-81-9
Ester β-1-adamantyle de l'acide Fmoc-L-aspartique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Asp(O-1-Ada)-OH
Documents
$82.02 /100 mg
Taille
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Informations sur le produit

Fmoc-L-aspartic acid b-1-adamantyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This derivative of aspartic acid features a protective Fmoc group, enhancing its stability and facilitating its incorporation into peptide chains. The unique adamantyl moiety not only contributes to the compound's hydrophobic properties but also improves the overall bioavailability of peptides in pharmaceutical applications. Researchers often leverage this compound in the synthesis of bioactive peptides, which can serve as potential therapeutics in various fields, including oncology and neurology.

The compound's ability to enhance solubility and stability makes it particularly valuable in the development of peptide-based drugs. Its application extends to the creation of peptide libraries for high-throughput screening, enabling the discovery of novel therapeutic agents. With its favorable properties, Fmoc-L-aspartic acid b-1-adamantyl ester stands out as an essential tool for researchers aiming to innovate in drug design and development, making it a preferred choice in both academic and industrial laboratories.

Numéro CAS 
118534-81-9
Formule moléculaire
C 29 H 316
Poids moléculaire 
489.5
Point de fusion 
52 - 67 °C
Rotation optique 
[a] D 25 = 33,0 ± 2 º (C = 1 dans CHCl 3 )
Informations générales
Numéro CAS 
118534-81-9
Formule moléculaire
C 29 H 316
Poids moléculaire 
489.5
Point de fusion 
52 - 67 °C
Rotation optique 
[a] D 25 = 33,0 ± 2 º (C = 1 dans CHCl 3 )
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-L-aspartic acid b-1-adamantyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without interfering with other functional groups. This is crucial for creating complex peptides used in pharmaceuticals.
  • Drug Development: Its unique structure enhances the solubility and stability of drug candidates, making it an important component in the formulation of new therapeutic agents, particularly in the field of oncology.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: Due to its structural properties, it is employed in studies related to neurotransmitter pathways, aiding in the understanding of neurological disorders and potential treatments.
  • Material Science: The compound is also explored in the development of new materials, particularly in creating polymers that require specific functional groups for enhanced performance in various applications.

Citations