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Catalog Number:
02414
CAS Number:
86061-04-3
Ester γ- tert -butylique et ester α-pentafluorophénylique de l'acide Fmoc-L-glutamique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Glu(OtBu)-OPfp
Documents
$29.34 /1G
Taille
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Informations sur le produit

Fmoc-L-glutamic acid g-tert-butyl ester a-pentafluorophenyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique structure that enhances its stability and solubility, making it an ideal choice for researchers in the fields of medicinal chemistry and biochemistry. Its Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for selective deprotection during peptide synthesis, facilitating the assembly of complex peptides with high purity and yield. The presence of the pentafluorophenyl group further enhances its reactivity and compatibility with various coupling reagents, streamlining the synthesis process.

This compound is particularly beneficial in the development of pharmaceuticals, where precise control over peptide structure is crucial for efficacy and safety. Its unique properties enable researchers to explore novel therapeutic peptides, contributing to advancements in targeted drug delivery systems and biologically active compounds. With its robust performance in peptide synthesis, Fmoc-L-glutamic acid g-tert-butyl ester a-pentafluorophenyl ester stands out as a valuable tool for professionals aiming to innovate in drug design and development.

Numéro CAS 
86061-04-3
Formule moléculaire
C 30 H 26 F 5 NON 6
Poids moléculaire 
591.5
Point de fusion 
119-126 °C
Rotation optique 
[a] D 20 = -31 ± 2º (C = 1 dans DMF)
Informations générales
Numéro CAS 
86061-04-3
Formule moléculaire
C 30 H 26 F 5 NON 6
Poids moléculaire 
591.5
Point de fusion 
119-126 °C
Rotation optique 
[a] D 20 = -31 ± 2º (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 
-
Applications

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

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and facilitating the assembly of complex molecules in pharmaceutical research.
  • Drug Development: Its unique structure enhances the solubility and stability of drug candidates, making it valuable in the formulation of new therapeutic agents, particularly in oncology.
  • Bioconjugation: The compound is used in bioconjugation techniques to attach drugs or imaging agents to biomolecules, improving targeted delivery systems in medical applications.
  • Research in Neuroscience: It plays a role in studying neurotransmitter pathways by serving as a building block for compounds that mimic or interact with glutamate receptors.
  • Material Science: The chemical is explored in the development of advanced materials, such as polymers and coatings, due to its unique chemical properties that enhance material performance.

Citations