Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
02413
CAS Number:
204251-24-1, 71989-18-9
Ester γ- tert -butylique hydraté d'acide Fmoc-L-glutamique
Purity:
≥ 99,7 % (HPLC chirale)
Synonym(s):
Fmoc-L-Glu(OtBu)-OH hydraté, Ester 5- tert -butylique hydraté d'acide Fmoc-L-glutamique
Documents
$20.20 /5G
Taille
Request Bulk Quote
Informations sur le produit

Fmoc-L-glutamic acid g-tert-butyl ester hydrate is a versatile amino acid derivative widely utilized in peptide synthesis and pharmaceutical research. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which is essential for the selective protection of the amino group during the synthesis of peptides. Its tert-butyl ester functionality enhances solubility and stability, making it an ideal choice for various organic synthesis applications. Researchers appreciate its role in facilitating the formation of complex peptides, which are crucial in drug development and biochemistry.

In addition to its applications in peptide synthesis, Fmoc-L-glutamic acid g-tert-butyl ester hydrate is also valuable in the study of protein interactions and enzyme activity. Its unique structure allows for the exploration of glutamic acid's role in biological systems, providing insights into metabolic pathways and potential therapeutic targets. This compound stands out for its ease of use and effectiveness in producing high-purity peptides, making it a preferred choice among professionals in the fields of medicinal chemistry and biochemistry.

Numéro CAS 
204251-24-1, 71989-18-9
Formule moléculaire
C24H27NO6 · H2O
Poids moléculaire 
443.49
Point de fusion 
80 - 100 °C
Rotation optique 
[a] D 20 = -8,5 ± 2 º (C = 1 dans MeOH)
Informations générales
Numéro CAS 
204251-24-1, 71989-18-9
Formule moléculaire
C24H27NO6 · H2O
Poids moléculaire 
443.49
Point de fusion 
80 - 100 °C
Rotation optique 
[a] D 20 = -8,5 ± 2 º (C = 1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Fmoc-L-glutamic acid g-tert-butyl ester hydrate is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids while preventing unwanted reactions.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in creating compounds that target specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in developing biosensors and drug delivery systems.
  • Research in Neuroscience: Its derivatives are often employed in studies related to neurotransmitter signaling, helping researchers explore the role of glutamate in brain function and disorders.
  • Material Science: The compound is also explored in the development of new materials, particularly in creating polymers that require specific functional groups for enhanced properties.

Citations