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Catalog Number:
15092
CAS Number:
738625-30-4
4-Fmoc-1-caboximetil-piperazin-2-ona
Purity:
≥ 98 % (HPLC)
Documents
$155.00 /100 mg
Tamaño
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Product Information

4-Fmoc-1-carboxymethyl-piperazin-2-one is a versatile compound widely utilized in peptide synthesis and drug development. This molecule features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an invaluable tool for researchers in the fields of medicinal chemistry and biochemistry. The compound's stability under various reaction conditions enhances its applicability in complex synthetic pathways, enabling the production of diverse peptide sequences with high purity and yield.

In addition to its role in peptide synthesis, 4-Fmoc-1-carboxymethyl-piperazin-2-one is also explored for its potential in drug formulation and delivery systems. Its ability to form stable complexes with various biomolecules opens avenues for targeted therapies and improved bioavailability of pharmaceutical agents. Researchers appreciate its ease of use and compatibility with standard laboratory protocols, making it a preferred choice for those looking to streamline their synthesis processes while achieving high-quality results.

CAS Number
738625-30-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C21H20N2O5
Molecular Weight
380.4
MDL Number
MFCD05663772
PubChem ID
17040176
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
738625-30-4
Purity
≥ 98 % (HPLC)
Molecular Formula
C21H20N2O5
Molecular Weight
380.4
MDL Number
MFCD05663772
PubChem ID
17040176
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Fmoc-1-caboxymethyl-piperazin-2-one is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing chemists to selectively modify amino acids without interfering with other functional groups.
  • Drug Development: It is employed in the design of novel pharmaceutical compounds, particularly in creating targeted therapies that can improve efficacy and reduce side effects.
  • Bioconjugation: The compound is useful in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools.
  • Research in Neuroscience: It is applied in studies related to neuropharmacology, aiding in the development of compounds that can interact with specific receptors in the brain.
  • Material Science: The compound finds applications in the development of smart materials, where its unique properties can be utilized to create responsive systems for various industrial applications.

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