Découvrez le nouveau Chem-Impex : là où l'innovation commence par une liaison.

Catalog Number:
00036
CAS Number:
54631-81-1
Boc -O -benzyl-L- trans -4-hydroxyproline
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Hyp(Bzl)-OH
Documents
$37.96 /1G
Taille
Request Bulk Quote
Informations sur le produit

Boc-O-benzyl-L-trans-4-hydroxyproline is a versatile amino acid derivative that plays a significant role in peptide synthesis and pharmaceutical development. This compound is particularly valued for its ability to serve as a protecting group in the synthesis of complex peptides, allowing for the selective modification of amino acids without compromising the integrity of the overall structure. Its unique structure enhances stability and solubility, making it an ideal choice for researchers focused on drug design and development.

In addition to its applications in synthetic chemistry, Boc-O-benzyl-L-trans-4-hydroxyproline is also utilized in the production of biologically active compounds, including those with potential therapeutic effects. Its compatibility with various coupling reagents and its ability to facilitate the formation of peptide bonds make it a preferred choice among chemists and biochemists. The compound's properties not only streamline the synthesis process but also improve yields, making it an essential tool for professionals in the pharmaceutical and biotechnology industries.

Numéro CAS 
54631-81-1
Formule moléculaire
C 17 H 235
Poids moléculaire 
321.38
Rotation optique 
[α] D 25 = -40 ± 2º (C=2 dans EtOH)
Informations générales
Numéro CAS 
54631-81-1
Formule moléculaire
C 17 H 235
Poids moléculaire 
321.38
Rotation optique 
[α] D 25 = -40 ± 2º (C=2 dans EtOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Boc-O-benzyl-L-trans-4-hydroxyproline is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly those requiring specific stereochemistry. Its unique structure allows for the introduction of hydroxyl groups, enhancing the stability and functionality of the resultant peptides.
  • Drug Development: In pharmaceutical research, it is used to create novel drug candidates, especially in the development of treatments for conditions like cancer and neurological disorders. Its ability to mimic natural amino acids makes it an attractive option for designing biologically active compounds.
  • Material Science: The compound is applied in the development of advanced materials, including hydrogels and polymers. Its properties can improve the mechanical strength and biocompatibility of these materials, making them suitable for biomedical applications.
  • Biotechnology: Researchers utilize it in the modification of proteins and enzymes, enhancing their activity or stability. This is particularly beneficial in industrial biotechnology, where optimized enzymes can lead to more efficient processes.
  • Analytical Chemistry: It is employed as a standard in various analytical methods, aiding in the quantification and characterization of complex mixtures. This application is crucial for ensuring the accuracy and reliability of experimental results.

Citations