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Catalog Number:
12394
CAS Number:
204269-35-2
Fmoc- O -allyl-D-tyrosine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Tyr(Tous)-OH
Documents
$36.65 /1G
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Informations sur le produit

Fmoc-O-allyl-D-tyrosine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis process. Its unique allyl side chain enhances its reactivity and provides additional functionalization options, making it an excellent choice for researchers focused on developing complex peptides and biologically active compounds.

In the pharmaceutical industry, Fmoc-O-allyl-D-tyrosine is particularly valuable for its role in the synthesis of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its properties allow for efficient coupling reactions, leading to higher yields and purities in peptide synthesis. Additionally, the compound's structural features enable its use in various applications, including the development of enzyme inhibitors and targeted drug delivery systems. Researchers will find that Fmoc-O-allyl-D-tyrosine not only simplifies the synthesis process but also enhances the overall efficiency of their projects.

Numéro CAS 
204269-35-2
Formule moléculaire
C 27 H 255
Poids moléculaire 
443.5
Point de fusion 
145-155 °C
Rotation optique 
[a] D 20 = +22,0 à +25,0º (C=1 dans DMF)
Informations générales
Numéro CAS 
204269-35-2
Formule moléculaire
C 27 H 255
Poids moléculaire 
443.5
Point de fusion 
145-155 °C
Rotation optique 
[a] D 20 = +22,0 à +25,0º (C=1 dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
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Applications

Fmoc-O-allyl-D-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly those targeting specific receptors or pathways.
  • Bioconjugation: The allyl group allows for selective reactions, making it useful in bioconjugation processes where precise attachment of biomolecules is required.
  • Research in Neuroscience: This compound can be used in studies related to neurotransmitter functions, aiding in the understanding of various neurological conditions.
  • Material Science: Its chemical properties lend themselves to applications in creating novel materials, particularly in the development of smart polymers.

Citations