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Catalog Number:
30799
CAS Number:
1935981-35-3
Fmoc-N-(2-azidoetil)glicina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-Aeg(N3)-OH
Antibiotic
Documents
$82.02 /100 mg
Tamaño
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Product Information

Fmoc-N-(2-azidoethyl)glycine is a versatile compound widely utilized in peptide synthesis and bioconjugation applications. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. The azidoethyl side chain enhances its utility in click chemistry, allowing for efficient conjugation reactions with various biomolecules, including proteins and nucleic acids. Researchers in the fields of medicinal chemistry and biochemistry can leverage this compound for developing novel therapeutics and studying protein interactions.

The unique properties of Fmoc-N-(2-azidoethyl)glycine make it particularly advantageous for applications in drug discovery and development. Its ability to facilitate the incorporation of azide functionalities into peptides opens up avenues for creating complex molecular architectures. This compound is also valuable in the synthesis of labeled peptides for imaging studies, providing insights into biological processes. With its robust performance in diverse applications, Fmoc-N-(2-azidoethyl)glycine stands out as a crucial tool for researchers aiming to innovate in the life sciences.

Synonyms
Fmoc-Aeg(N3)-OH
CAS Number
1935981-35-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD30491715
PubChem ID
127239815
Melting Point
107 - 113 °C
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-Aeg(N3)-OH
CAS Number
1935981-35-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C19H18N4O4
Molecular Weight
366.4
MDL Number
MFCD30491715
PubChem ID
127239815
Melting Point
107 - 113 °C
Appearance
Polvo cristalino blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
DEA-regulated
No
Warnings
-
Applications

Fmoc-N-(2-azidoethyl)glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, where its protective Fmoc group allows for selective deprotection and functionalization.
  • Bioconjugation: The azide group enables click chemistry applications, allowing researchers to easily attach biomolecules, such as proteins or nucleic acids, to surfaces or other molecules, enhancing drug delivery systems.
  • Drug Development: It plays a crucial role in the design of novel therapeutics, particularly in the development of peptide-based drugs that require specific modifications for improved efficacy and targeting.
  • Material Science: Used in the creation of functionalized polymers, it helps in developing advanced materials with tailored properties for applications in coatings, adhesives, and sensors.
  • Diagnostics: The compound can be utilized in the development of diagnostic tools, where its ability to form stable conjugates with biomolecules aids in the detection of diseases through targeted imaging techniques.

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