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Catalog Number:
33468
CAS Number:
432507-62-5
Fmoc-EDA-N 3
Purity:
≥ 99 % (HPLC)
Synonym(s):
N- (2-azidoetil)carbamato de 9H -fluoren-9-ilmetilo
Antibiotic
Documents
$51.18 /100 mg
Tamaño
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Información del producto

Fmoc-EDA-N3 is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This chemical, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, serves as an essential building block in peptide synthesis, particularly in the development of azide-functionalized peptides. Its unique azido group allows for further modifications through click chemistry, making it an invaluable tool for researchers aiming to create complex molecular architectures.

In addition to its applications in peptide synthesis, Fmoc-EDA-N3 is also employed in bioconjugation processes, enabling the attachment of various biomolecules for drug delivery and imaging applications. The compound's stability and ease of handling make it a preferred choice among professionals in the pharmaceutical and biotechnology industries. With its ability to facilitate the synthesis of diverse compounds, Fmoc-EDA-N3 stands out as a key reagent for advancing research and development in various chemical and biological applications.

Número CAS
432507-62-5
Fórmula molecular
C17H16N4O2
Peso molecular
308.3
Número MDL
MFCD31380731
Punto de fusión
99-101 °C
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
432507-62-5
Fórmula molecular
C17H16N4O2
Peso molecular
308.3
Número MDL
MFCD31380731
Punto de fusión
99-101 °C
Condiciones
Conservar entre 2 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

Fmoc-EDA-N3 is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions while preventing unwanted side reactions. Its stability under various conditions makes it a preferred choice for researchers.
  • Bioconjugation: Fmoc-EDA-N3 is instrumental in bioconjugation processes, where it facilitates the attachment of biomolecules to surfaces or other molecules. This is particularly valuable in drug development and diagnostics.
  • Click Chemistry: The azide functional group in Fmoc-EDA-N3 enables its use in click chemistry, a powerful tool for creating complex molecules quickly and efficiently. This application is crucial in materials science and medicinal chemistry.
  • Fluorescent Probes: Researchers utilize this compound to develop fluorescent probes for imaging applications. Its properties allow for the tracking of biological processes in real-time, enhancing our understanding of cellular functions.
  • Drug Delivery Systems: Fmoc-EDA-N3 is explored in the design of drug delivery systems, where it can help in the controlled release of therapeutic agents, improving the efficacy and safety of treatments.

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