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Catalog Number:
01404
CAS Number:
2799-07-7
S -Trityl-L-cystéine
Purity:
≥ 98 % (HPLC)
Synonym(s):
L-Cys(Trt)-OH, (+)- S -Trityl-L-cystéine
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Informations sur le produit

S-Trityl-L-cysteine is a versatile thiol compound that plays a crucial role in biochemical research and pharmaceutical applications. Known for its unique trityl protecting group, this compound is particularly valuable in peptide synthesis and the development of cysteine derivatives. Its ability to stabilize reactive thiol groups makes it an essential reagent in the preparation of various bioactive molecules, including peptides and proteins. Researchers appreciate S-Trityl-L-cysteine for its effectiveness in facilitating selective reactions, which can lead to higher yields and purities in synthetic processes.

In addition to its applications in organic synthesis, S-Trityl-L-cysteine is also explored for its potential in drug development, particularly in the design of therapeutics targeting cysteine-rich proteins. Its favorable properties, such as solubility and stability, enhance its usability in diverse experimental conditions. Whether you are involved in academic research or industrial applications, S-Trityl-L-cysteine offers significant advantages in the synthesis of complex molecules, making it an indispensable tool in modern chemistry.

Numéro CAS 
2799-07-7
Formule moléculaire
C 22 H 21 NO 2 S
Poids moléculaire 
363.5
Point de fusion 
155-170 °C
Rotation optique 
[a] D 20 = +113 ± 6º (C = 0,8 % dans 0,04 M HCl éthanolique)
Informations générales
Numéro CAS 
2799-07-7
Formule moléculaire
C 22 H 21 NO 2 S
Poids moléculaire 
363.5
Point de fusion 
155-170 °C
Rotation optique 
[a] D 20 = +113 ± 6º (C = 0,8 % dans 0,04 M HCl éthanolique)
Propriétés
Informations complémentaires sur la propriété à venir prochainement !
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Sécurité et réglementation
Matières dangereuses
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Antibiotique
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Réglementé par la DEA
Non
Avertissements 
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Applications

S-Trityl-L-cysteine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for cysteine residues in peptide synthesis, allowing for the selective modification of other amino acids without affecting the cysteine. This is crucial in developing complex peptides used in pharmaceuticals.
  • Drug Development: It plays a role in the design of novel drugs, particularly in creating compounds that target specific biological pathways. Its unique structure can enhance the stability and efficacy of therapeutic agents.
  • Bioconjugation: S-Trityl-L-cysteine is utilized in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, improving the delivery and targeting of drugs in cancer therapy.
  • Research in Protein Engineering: This compound is essential in protein engineering, allowing researchers to create proteins with enhanced properties, such as increased stability or altered activity, which can be beneficial in various industrial applications.
  • Analytical Chemistry: It is used in analytical methods to study protein interactions and modifications, providing insights into biochemical processes that are vital for understanding diseases and developing new treatments.

Citations