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Catalog Number:
07362
CAS Number:
269078-84-4
Fmoc-4-carboxymethyl-1,2,3,4-tetrahydroquinoxalin-3-one
Purity:
≥ 97% (HPLC)
Documents
$120.88 /100MG
Pack Size Availability Price
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Product Information

Fmoc-4-carboxymethyl-1,2,3,4-tetrahydroquinoxalin-3-one is a versatile compound widely utilized in the field of peptide synthesis and medicinal chemistry. This compound, known for its protective Fmoc (9-fluorenylmethoxycarbonyl) group, offers significant advantages in the solid-phase peptide synthesis process, allowing for the efficient assembly of complex peptides. Its unique structure not only enhances stability during synthesis but also facilitates the selective deprotection of amino acids, making it an essential tool for researchers aiming to develop novel therapeutic peptides.

In addition to its role in peptide synthesis, Fmoc-4-carboxymethyl-1,2,3,4-tetrahydroquinoxalin-3-one has shown potential in various research applications, including drug discovery and development. Its ability to act as a building block for bioactive compounds opens avenues for creating targeted therapies in areas such as cancer and neurodegenerative diseases. Researchers appreciate its compatibility with various coupling reagents and its ease of use in diverse synthetic pathways, making it a valuable asset in both academic and industrial laboratories.

CAS Number
269078-84-4
Purity
≥ 97% (HPLC)
Molecular Formula
C25H20N2O5
Molecular Weight
428.44
MDL Number
MFCD01321023
PubChem ID
2756217
Appearance
White amorphous powder
Conditions
Store at 0-8 °C
General Information
CAS Number
269078-84-4
Purity
≥ 97% (HPLC)
Molecular Formula
C25H20N2O5
Molecular Weight
428.44
MDL Number
MFCD01321023
PubChem ID
2756217
Appearance
White amorphous 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

Fmoc-4-carboxymethyl-1,2,3,4-tetrahydroquinoxalin-3-one is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a role in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound can be used to create bioconjugates, linking drugs to biomolecules for targeted delivery, which is crucial in cancer therapy and other treatments.
  • Analytical Chemistry: It is employed in the development of analytical methods to detect and quantify specific biomolecules, aiding in research and quality control in pharmaceuticals.
  • Material Science: The chemical is explored for its potential in creating advanced materials, such as sensors and coatings, due to its unique structural properties.

Citations