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Catalog Number:
02412
CAS Number:
123639-61-2
Ester γ-benzylique de l'acide Fmoc-L-glutamique
Purity:
≥ 99,5 % (HPLC chirale)
Synonym(s):
Fmoc-L-Glu(OBzl)-OH, Ester 5-benzylique de l'acide Fmoc-L-glutamique
Documents
$27.94 /5G
Taille
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Informations sur le produit

Fmoc-L-glutamic acid g-benzyl ester 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 process, making it an invaluable tool for researchers in the field of organic chemistry and biochemistry. Its unique structure not only enhances stability but also facilitates the formation of complex peptides, essential for various applications in pharmaceuticals and biotechnology.

The g-benzyl ester modification provides additional hydrophobic characteristics, improving solubility and enhancing the overall efficacy of peptide formulations. This compound is particularly beneficial in the synthesis of bioactive peptides, which can be used in therapeutic applications, including drug delivery systems and enzyme inhibitors. Researchers and industry professionals can leverage Fmoc-L-glutamic acid g-benzyl ester to streamline their synthesis processes, ensuring high yields and purity in their final products.

Numéro CAS 
123639-61-2
Formule moléculaire
C 27 H 256
Poids moléculaire 
459.5
Point de fusion 
126 - 146 ?C
Rotation optique 
[a] D 20 = 10 ± 5 º (C = 1 dans CHCl 3 )
Informations générales
Numéro CAS 
123639-61-2
Formule moléculaire
C 27 H 256
Poids moléculaire 
459.5
Point de fusion 
126 - 146 ?C
Rotation optique 
[a] D 20 = 10 ± 5 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-glutamic acid g-benzyl ester 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 protein structures efficiently.
  • Drug Development: It plays a crucial role in the pharmaceutical industry, particularly in developing new drugs that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Research in Neuroscience: Its derivatives are often employed in studies related to neurotransmitter signaling, helping scientists understand brain function and develop treatments for neurological disorders.
  • Material Science: The compound is also explored in creating advanced materials, such as hydrogels, which have applications in drug delivery systems and tissue engineering.

Citations