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

Catalog Number:
02735
CAS Number:
51077-16-8
Boc-L-thiaproline
Purity:
≥ 99 % (HPLC)
Synonym(s):
Boc-L-Thz-OH, Acide boc-L-thiazolidine-4-carboxylique
Documents
$18.53 /1G
Taille
Request Bulk Quote
Informations sur le produit

Boc-L-thiaproline is a valuable amino acid derivative widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique thiazolidine ring structure, which enhances its stability and bioactivity compared to traditional amino acids. Its protective Boc (tert-butyloxycarbonyl) group allows for selective reactions, making it an ideal choice for researchers looking to develop complex peptides with specific functionalities.

In the pharmaceutical industry, Boc-L-thiaproline has shown promise in the design of bioactive peptides and as a building block for drug candidates targeting various diseases. Its ability to mimic natural amino acids while providing distinct chemical properties opens avenues for innovative therapeutic applications. Researchers appreciate its versatility in synthetic pathways, as it can facilitate the incorporation of sulfur into peptide chains, which is crucial for the development of novel compounds with enhanced pharmacological profiles.

Numéro CAS 
51077-16-8
Formule moléculaire
C 9 H 15 NON 4 S
Poids moléculaire 
233.3
Point de fusion 
120 - 140 °C
Rotation optique 
[a] D 20 = -115 ± 5 ° (C = 1 dans MeOH)
Informations générales
Numéro CAS 
51077-16-8
Formule moléculaire
C 9 H 15 NON 4 S
Poids moléculaire 
233.3
Point de fusion 
120 - 140 °C
Rotation optique 
[a] D 20 = -115 ± 5 ° (C = 1 dans MeOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
-
Sécurité et réglementation
Matières dangereuses
-
Antibiotique
-
Réglementé par la DEA
Non
Avertissements 
-
Applications

Boc-L-thiaproline is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a valuable building block in the synthesis of peptides, particularly in the development of cyclic peptides that can enhance biological activity.
  • Drug Development: It plays a crucial role in medicinal chemistry, where it is used to design and synthesize novel drugs, especially those targeting specific receptors or enzymes.
  • Bioconjugation: Researchers leverage Boc-L-thiaproline for bioconjugation processes, allowing for the attachment of biomolecules to therapeutic agents, improving their efficacy and targeting capabilities.
  • Protein Engineering: Its unique structure aids in the modification of proteins, enabling scientists to create proteins with enhanced stability and functionality for various applications in biotechnology.
  • Research in Neuroscience: The compound is explored for its potential applications in neuroscience, particularly in studying the effects of modified peptides on neurological pathways and disorders.

Citations