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Catalog Number:
03617
CAS Number:
146982-30-1
Fmoc- O -allyl-L-tyrosine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Tyr(Tous)-OH
Documents
$22.03 /1G
Taille
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Informations sur le produit

Fmoc-O-allyl-L-tyrosine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (fluorenylmethyloxycarbonyl) group, which allows for selective deprotection during the synthesis of peptides, making it an essential building block for researchers in the field of medicinal chemistry. Its unique allyl group enhances the compound's reactivity and provides opportunities for further functionalization, enabling the creation of complex peptide structures with tailored properties.

In addition to its role in peptide synthesis, Fmoc-O-allyl-L-tyrosine is also valuable in the development of bioactive compounds and pharmaceuticals. Its ability to participate in various coupling reactions makes it a preferred choice for researchers looking to explore new therapeutic agents. The compound's stability and compatibility with standard coupling reagents further enhance its appeal, ensuring efficient and reliable synthesis processes. With its broad applications in both academic and industrial settings, Fmoc-O-allyl-L-tyrosine stands out as a crucial tool for advancing peptide-based research and drug discovery.

Numéro CAS 
146982-30-1
Formule moléculaire
C 27 H 255
Poids moléculaire 
443.5
Point de fusion 
140 - 150 °C
Rotation optique 
[a] D 25 = -21,1 ± 2 ° (C = 1 dans DMF)
Informations générales
Numéro CAS 
146982-30-1
Formule moléculaire
C 27 H 255
Poids moléculaire 
443.5
Point de fusion 
140 - 150 °C
Rotation optique 
[a] D 25 = -21,1 ± 2 ° (C = 1 dans DMF)
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-O-allyl-L-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the incorporation of unique functionalities that enhance the properties of the final product.
  • Drug Development: It plays a crucial role in the development of novel pharmaceuticals, particularly in designing compounds that target specific biological pathways, improving efficacy and selectivity.
  • Bioconjugation: Researchers use it for bioconjugation processes, linking biomolecules to create targeted drug delivery systems, which can improve therapeutic outcomes.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research for studying receptor interactions and signaling pathways, contributing to the understanding of neurological disorders.
  • Material Science: The compound is also applied in the development of smart materials, where its unique chemical properties can be utilized to create responsive systems for various applications.

Citations