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Catalog Number:
12136
CAS Number:
105526-85-0
O-Trityl-L-pyroglutaminol
Purity:
≥ 99% (HPLC)
Synonym(s):
(S-5-(Trityloxymethyl)-2-pyrrolidinone
Documents
$154.93 /1G
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Product Information

O-Trityl-L-pyroglutaminol is a versatile compound widely recognized for its applications in peptide synthesis and pharmaceutical research. This compound features a trityl protecting group, which enhances its stability and solubility, making it an ideal choice for chemists working on complex organic synthesis. Its unique structure allows for selective reactions, facilitating the development of novel therapeutic agents. Researchers often utilize O-Trityl-L-pyroglutaminol in the synthesis of bioactive peptides, contributing to advancements in drug discovery and development.

In addition to its role in peptide synthesis, O-Trityl-L-pyroglutaminol is also valuable in the study of enzyme mechanisms and protein interactions. Its ability to serve as a building block in the creation of intricate molecular architectures opens up new avenues for exploration in medicinal chemistry. With its favorable properties, O-Trityl-L-pyroglutaminol stands out as a crucial tool for professionals aiming to innovate in the fields of pharmaceuticals and biochemistry.

Synonyms
(S-5-(Trityloxymethyl)-2-pyrrolidinone
CAS Number
105526-85-0
Purity
≥ 99% (HPLC)
Molecular Formula
C24H23NO2
Molecular Weight
357.5
MDL Number
MFCD00075592
PubChem ID
3956841
Melting Point
162-167 °C
Appearance
White powder
Optical Rotation
[a]D20 = +10 ± 2º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
(S-5-(Trityloxymethyl)-2-pyrrolidinone
CAS Number
105526-85-0
Purity
≥ 99% (HPLC)
Molecular Formula
C24H23NO2
Molecular Weight
357.5
MDL Number
MFCD00075592
PubChem ID
3956841
Melting Point
162-167 °C
Appearance
White powder
Optical Rotation
[a]D20 = +10 ± 2º (C=1 in MeOH)
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

O-Trityl-L-pyroglutaminol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the development of new pharmaceuticals, particularly in designing compounds with improved bioavailability and stability.
  • Biochemical Research: Researchers use it to study protein interactions and enzyme mechanisms, providing insights into biological processes and potential therapeutic targets.
  • Organic Synthesis: The compound is employed in various organic synthesis reactions, enabling the creation of complex molecules with high specificity and yield.
  • Material Science: It is also explored in the development of advanced materials, including polymers and nanomaterials, due to its unique chemical properties.

Citations