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Catalog Number:
12435
CAS Number:
204251-86-5
Ester α-allylique de l'acide Fmoc-D-glutamique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Glu-OAll
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Informations sur le produit

Fmoc-D-glutamic acid a-allyl ester is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during the synthesis process while allowing for easy deprotection when needed. Its unique allyl ester functionality enhances its reactivity, making it an excellent choice for coupling reactions in the formation of complex peptides. Researchers and industry professionals appreciate its role in developing bioactive peptides, pharmaceuticals, and other biologically relevant compounds.

In addition to its utility in peptide synthesis, Fmoc-D-glutamic acid a-allyl ester is also employed in various applications within the fields of drug discovery and materials science. Its ability to facilitate the formation of peptide bonds while maintaining structural integrity makes it a valuable tool for creating novel therapeutic agents. The compound's favorable properties, such as solubility and stability, further enhance its appeal for researchers seeking reliable building blocks in their synthetic pathways.

Numéro CAS 
204251-86-5
Formule moléculaire
C 23 H 236
Poids moléculaire 
409.43
Point de fusion 
111 - 128 °C (lit.)
Rotation optique 
[a] D 20 = 18 ± 3 º (C = 1 dans DMF)
Informations générales
Numéro CAS 
204251-86-5
Formule moléculaire
C 23 H 236
Poids moléculaire 
409.43
Point de fusion 
111 - 128 °C (lit.)
Rotation optique 
[a] D 20 = 18 ± 3 º (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

Fmoc-D-glutamic acid a-allyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the creation of complex peptide structures.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, especially those targeting neurological disorders, due to its ability to mimic natural amino acids.
  • Bioconjugation: The allyl ester group enables selective reactions for bioconjugation, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted therapies.
  • Research in Neuroscience: It is used in studies related to neurotransmitter functions and signaling pathways, providing insights into brain function and potential treatments for cognitive disorders.
  • Material Science: The compound can be incorporated into polymer matrices to enhance material properties, making it useful in developing advanced materials for various applications.

Citations