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Catalog Number:
33468
CAS Number:
432507-62-5
Fmoc-EDA-N3
Purity:
≥ 99% (HPLC)
Synonym(s):
9H-Fluoren-9-ylmethyl N-(2-azidoethyl)carbamate
Antibiotic
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$51.18 /100MG
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Product Information

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.

Synonyms
9H-Fluoren-9-ylmethyl N-(2-azidoethyl)carbamate
CAS Number
432507-62-5
Purity
≥ 99% (HPLC)
Molecular Formula
C17H16N4O2
Molecular Weight
308.3
MDL Number
MFCD31380731
PubChem ID
16751906
Melting Point
99 - 101 ?C
Appearance
White crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
9H-Fluoren-9-ylmethyl N-(2-azidoethyl)carbamate
CAS Number
432507-62-5
Purity
≥ 99% (HPLC)
Molecular Formula
C17H16N4O2
Molecular Weight
308.3
MDL Number
MFCD31380731
PubChem ID
16751906
Melting Point
99 - 101 ?C
Appearance
White crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
Yes
DEA-regulated
No
Warnings
-
Applications

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.

Citations