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Catalog Number:
01964
CAS Number:
154445-77-9
N α - Fmoc- N ω -(2,2,4,6,7-pentaméthyldihydro-benzofuran-5-sulfonyl)-L-arginine
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-L-Arg(Pbf)-OH
Documents
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Taille
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Informations sur le produit
Numéro CAS 
154445-77-9
Formule moléculaire
C34H40N4O7S
Poids moléculaire 
648.77
Point de fusion 
132 °C (déc.)
Rotation optique 
[a] D 25 = -4 ± 3 º (C = 4 dans DMF) D 20 = -4 ± 1 º (C = 1 dans DMF)
Informations générales
Numéro CAS 
154445-77-9
Formule moléculaire
C34H40N4O7S
Poids moléculaire 
648.77
Point de fusion 
132 °C (déc.)
Rotation optique 
[a] D 25 = -4 ± 3 º (C = 4 dans DMF) D 20 = -4 ± 1 º (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

Na-Fmoc-Nw-(2,2,4,6,7-pentamethyldihydrobenzofuran-5-sulfonyl)-L-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids. Its stability under various conditions makes it ideal for complex peptide sequences.
  • Drug Development: In pharmaceutical research, it aids in the design of peptide-based drugs, particularly those targeting specific receptors. Its unique structure enhances binding affinity and specificity.
  • Bioconjugation: The sulfonyl group allows for efficient conjugation with biomolecules, facilitating the development of targeted delivery systems in therapeutics, particularly in cancer treatment.
  • Research in Neuroscience: This compound can be used in studies related to neuropeptides, helping researchers understand signaling pathways and potential therapeutic targets for neurological disorders.
  • Analytical Chemistry: It is useful in the development of analytical methods for detecting and quantifying peptides in biological samples, providing insights into metabolic processes and disease states.

Citations