Descubra el nuevo Chem-Impex: donde la innovación comienza con un vínculo.

Catalog Number:
33497
CAS Number:
2137142-63-1
Fmoc-(4 S )-4-azido-D-prolina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Pro(4-N3)-OH ( 2R , 4S ), Fmoc-(2 R ,4 S )-4-azidoprolina
Antibiotic
Documents
$60.00 /25 mg
Tamaño
Request Bulk Quote
Información del producto

Fmoc-(4S)-4-Azido-D-Proline is a versatile building block widely used in peptide synthesis and medicinal chemistry. This compound features a unique azido group that enhances its reactivity, making it an excellent candidate for click chemistry applications. Its Fmoc protecting group allows for easy incorporation into peptide sequences, facilitating the synthesis of complex peptides and proteins. Researchers appreciate its utility in the development of bioactive compounds, particularly in the fields of drug discovery and development, where it can be employed to create novel therapeutics with enhanced efficacy.

The compound's specific stereochemistry and functional groups enable selective modifications, allowing for the introduction of diverse functionalities into peptide chains. This makes Fmoc-(4S)-4-Azido-D-Proline particularly valuable for applications in targeted drug delivery and the design of peptide-based vaccines. Its ability to participate in various coupling reactions further expands its applicability in the synthesis of peptide libraries, providing researchers with a powerful tool for exploring structure-activity relationships in drug development.

Número CAS
2137142-63-1
Fórmula molecular
C20H18N4O4
Peso molecular
378.4
Número MDL
MFCD31380719
Punto de fusión
140 - 144 °C
Rotación óptica
[a] 20 D = 35 ± 1 ° (C = 1 en DMF)
Condiciones
Conservar entre 2 y 8 °C.
Información general
Número CAS
2137142-63-1
Fórmula molecular
C20H18N4O4
Peso molecular
378.4
Número MDL
MFCD31380719
Punto de fusión
140 - 144 °C
Rotación óptica
[a] 20 D = 35 ± 1 ° (C = 1 en DMF)
Condiciones
Conservar entre 2 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
-
Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

Fmoc-(4S)-4-Azido-D-Proline is widely utilized in research focused on:

  • Peptide Synthesis: This compound is commonly used in the synthesis of peptides, particularly in the development of new therapeutic agents. Its unique azido group allows for selective modifications, enhancing the versatility of peptide design.
  • Bioconjugation: The azido group facilitates click chemistry reactions, making it ideal for bioconjugation applications. This is particularly useful in drug delivery systems and the development of targeted therapies.
  • Protein Labeling: Researchers employ this compound for labeling proteins with fluorescent tags or other markers. This application is essential in studying protein interactions and dynamics in cellular environments.
  • Drug Development: Its role in the synthesis of novel compounds makes it valuable in pharmaceutical research, especially in creating molecules with improved efficacy and selectivity for specific biological targets.
  • Material Science: The compound is also explored in the field of material science for developing smart materials that respond to environmental stimuli, leveraging its unique chemical properties.

Citas