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Catalog Number:
30455
CAS Number:
158009-03-1
Chlorhydrate d'ester tert -butylique de S -Trityl-L-Cystéine
Purity:
≥ 99 % (HPLC)
Synonym(s):
HL-Cys(Trt)-OtBu·HCl
Documents
$100.00 /1G
Taille
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Informations sur le produit

S-Trityl-L-cystine tert-butyl ester hydrochloride is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound, recognized for its unique trityl protecting group, facilitates the selective modification of cysteine residues in peptides and proteins, making it invaluable for researchers focusing on peptide synthesis and protein engineering. Its stability under various reaction conditions allows for the development of complex molecular architectures, enhancing its appeal in drug discovery and development.

In addition to its role in peptide synthesis, S-Trityl-L-cystine tert-butyl ester hydrochloride serves as a crucial intermediate in the preparation of biologically active compounds. Its ability to protect thiol groups while maintaining reactivity in other functional groups opens avenues for the design of novel therapeutics. Researchers appreciate its ease of use and the efficiency it brings to synthetic pathways, making it a preferred choice for those aiming to streamline their workflows in both academic and industrial settings.

Numéro CAS 
158009-03-1
Formule moléculaire
C26H30ClNO2S
Poids moléculaire 
456.0
Point de fusion 
68-74 °C
Rotation optique 
[a] D 20 = +79 ± 2º (C = 1 dans 96 % d'EtOH)
Informations générales
Numéro CAS 
158009-03-1
Formule moléculaire
C26H30ClNO2S
Poids moléculaire 
456.0
Point de fusion 
68-74 °C
Rotation optique 
[a] D 20 = +79 ± 2º (C = 1 dans 96 % d'EtOH)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
-
Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

S-Trityl-L-cystine tert-butyl ester hydrochloride is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing researchers to selectively modify amino acids without affecting others, thereby enhancing the efficiency of drug development.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems in pharmaceuticals.
  • Antioxidant Research: The compound is studied for its potential antioxidant properties, making it relevant in the development of supplements and formulations aimed at reducing oxidative stress in biological systems.
  • Protein Stabilization: In protein chemistry, it helps stabilize proteins during purification and analysis, which is essential for ensuring the integrity of therapeutic proteins in biopharmaceuticals.
  • Diagnostic Applications: Its role in developing diagnostic tools, particularly in assays that detect specific biomolecules, showcases its importance in clinical research and diagnostics.

Citations