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Catalog Number:
16577
CAS Number:
88109-06-2
Trityl-L-sérine lactone
Purity:
≥ 98 % (HPLC)
Synonym(s):
( S -3-(tritylamino)-2-oxétanone
Documents
$106.96 /250 mg
Taille
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Informations sur le produit

Trityl-L-serine lactone is a versatile compound recognized for its unique structural features and functional applications in various fields, particularly in organic synthesis and pharmaceutical development. This lactone derivative of L-serine is characterized by its trityl group, which enhances its stability and solubility, making it an ideal candidate for peptide synthesis and modification. Researchers often utilize Trityl-L-serine lactone in the preparation of protected amino acids, facilitating the construction of complex peptides and proteins. Its ability to serve as a protecting group for the amino functionality allows for selective reactions, streamlining synthetic pathways in peptide chemistry.

In addition to its role in peptide synthesis, Trityl-L-serine lactone is also explored for its potential applications in drug formulation and delivery systems. The compound's favorable properties, such as its stability under various conditions and compatibility with different solvents, make it a valuable asset in the development of novel therapeutic agents. By incorporating Trityl-L-serine lactone into their research, scientists can enhance the efficiency and specificity of their synthetic processes, ultimately leading to the advancement of innovative solutions in medicinal chemistry.

Numéro CAS 
88109-06-2
Formule moléculaire
C 22 H 19 NO 2
Poids moléculaire 
329.39
Point de fusion 
179-183 °C
Informations générales
Numéro CAS 
88109-06-2
Formule moléculaire
C 22 H 19 NO 2
Poids moléculaire 
329.39
Point de fusion 
179-183 °C
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

Trityl-L-serine lactone is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group for amino acids during peptide synthesis, allowing for the selective modification of specific functional groups without interfering with others.
  • Drug Development: It plays a crucial role in the development of pharmaceuticals, particularly in creating compounds that require specific stereochemistry for optimal biological activity.
  • Bioconjugation: Trityl-L-serine lactone is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the efficacy of drugs and diagnostics.
  • Research in Neuroscience: The compound is valuable in studying neurotransmitter systems due to its ability to modify serine residues in proteins, which can influence receptor activity and signaling pathways.
  • Material Science: It is also explored in the development of novel materials, particularly in creating polymers with specific functionalities that can be tailored for various applications.

Citations