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Catalog Number:
16577
CAS Number:
88109-06-2
Trityl-L-serine lactone
Purity:
≥ 98% (HPLC)
Synonym(s):
(S-3-(Tritylamino)-2-oxetanone
Documents
$106.96 /250MG
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Product Information

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.

Synonyms
(S-3-(Tritylamino)-2-oxetanone
CAS Number
88109-06-2
Purity
≥ 98% (HPLC)
Molecular Formula
C22H19NO2
Molecular Weight
329.39
MDL Number
MFCD00270148
PubChem ID
4290083
Melting Point
179-183 °C
Appearance
White powder
Conditions
Store at 0-8 °C
General Information
Synonyms
(S-3-(Tritylamino)-2-oxetanone
CAS Number
88109-06-2
Purity
≥ 98% (HPLC)
Molecular Formula
C22H19NO2
Molecular Weight
329.39
MDL Number
MFCD00270148
PubChem ID
4290083
Melting Point
179-183 °C
Appearance
White powder
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
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