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Catalog Number:
02410
CAS Number:
210645-01-5
N α - Fmoc- N δ -4,4'-diméthoxybenzhydryl-D-glutamine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-Nδ-4,4'-diméthoxybenzhydryl-D-glutamine
Documents
$89.13 /1G
Taille
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Informations sur le produit

Na-Fmoc-Nd-4,4'-dimethoxybenzhydryl-D-glutamine is a specialized 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 amino groups during solid-phase peptide synthesis. Its unique structure, characterized by the presence of dimethoxybenzyl and glutamine moieties, enhances its stability and solubility, making it an ideal choice for researchers focused on synthesizing complex peptides and biologically active compounds.

In the pharmaceutical industry, Na-Fmoc-Nd-4,4'-dimethoxybenzhydryl-D-glutamine serves as a valuable building block for the development of peptide-based therapeutics, particularly in the fields of oncology and immunology. Its ability to facilitate the incorporation of specific amino acids into peptide chains allows for the creation of tailored molecules with enhanced efficacy and reduced side effects. Researchers appreciate its versatility and effectiveness in producing high-purity peptides, which are crucial for advancing drug discovery and development processes.

Numéro CAS 
210645-01-5
Formule moléculaire
C35H34N2O7
Poids moléculaire 
594.7
Point de fusion 
160-180 °C
Rotation optique 
[a] D 25 = +6,5 ± 1,5º (C = 1 % dans DMF)
Informations générales
Numéro CAS 
210645-01-5
Formule moléculaire
C35H34N2O7
Poids moléculaire 
594.7
Point de fusion 
160-180 °C
Rotation optique 
[a] D 25 = +6,5 ± 1,5º (C = 1 % dans DMF)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
-
Applications

Na-Fmoc-Nd-4,4'-dimethoxybenzhydryl-D-glutamine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with the overall peptide structure.
  • Drug Development: Its unique structure aids in the design of peptide-based drugs, particularly in enhancing the stability and bioavailability of therapeutic peptides.
  • Bioconjugation: The chemical is useful in bioconjugation processes, where it facilitates the attachment of peptides to other biomolecules, improving the efficacy of drug delivery systems.
  • Research in Neuroscience: It can be employed in studies related to neuropeptides, helping researchers understand their roles in neurological functions and potential therapeutic applications.
  • Analytical Chemistry: This compound is valuable in analytical methods for characterizing peptide structures, providing insights into their properties and interactions.

Citations