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Catalog Number:
05471
CAS Number:
200122-49-2
N α - Boc- N ω -(4-méthoxy-2,3,6-triméthylbenzènesulfonyl)-D-arginine
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-D-Arg(Mtr)-OH
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$74.81 /1G
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Informations sur le produit

Na-Boc-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine is a specialized amino acid derivative that plays a crucial role in peptide synthesis and drug development. This compound is particularly valued in the pharmaceutical industry for its ability to enhance the solubility and stability of peptides, making it an essential building block for researchers focused on developing new therapeutic agents. Its unique structure, featuring a protective Boc group and a sulfonyl moiety, allows for selective reactions, facilitating the synthesis of complex molecules with high specificity.

In addition to its applications in drug design, Na-Boc-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine is also utilized in the development of bioconjugates and targeted delivery systems, where its properties can be leveraged to improve the efficacy of active pharmaceutical ingredients. Researchers appreciate its compatibility with various coupling reactions, which streamlines the process of synthesizing novel compounds. With its unique features and practical applications, this compound stands out as a valuable asset for professionals in medicinal chemistry and related fields.

Numéro CAS 
200122-49-2
Formule moléculaire
C21H34N4O7S
Poids moléculaire 
486.68
Point de fusion 
92-97 °C
Rotation optique 
[a] D 20
Informations générales
Numéro CAS 
200122-49-2
Formule moléculaire
C21H34N4O7S
Poids moléculaire 
486.68
Point de fusion 
92-97 °C
Rotation optique 
[a] D 20
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Na-Boc-Nw-(4-methoxy-2,3,6-trimethylbenzenesulfonyl)-D-arginine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, enhancing the stability and efficiency of reactions, which is crucial for developing new therapeutic peptides.
  • Drug Development: It plays a significant role in the design of novel pharmaceuticals, particularly in targeting specific biological pathways, thereby improving drug efficacy and reducing side effects.
  • Bioconjugation: The compound is useful in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in creating targeted drug delivery systems.
  • Diagnostics: It can be employed in the development of diagnostic tools, particularly in assays that require high specificity and sensitivity, thus aiding in early disease detection.
  • Research in Molecular Biology: This chemical is valuable in molecular biology studies, particularly in understanding protein interactions and functions, which can lead to breakthroughs in disease treatment.

Citations