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Catalog Number:
15723
CAS Number:
959578-11-1
Ácido fmoc-L-2-amino-5-fenilpentanoico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Nva(5-fenil)-OH, Fmoc-Nva(5-fenil)-OH
Documents
$80.50 /250 mg
Tamaño
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Información del producto

Fmoc-L-2-amino-5-phenylpentanoic acid is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound, recognized for its protective Fmoc (9-fluorenylmethoxycarbonyl) group, facilitates the efficient assembly of peptides by providing a stable and easily removable protective group during solid-phase synthesis. Its unique structure, featuring a phenyl side chain, enhances the hydrophobic interactions within peptides, making it particularly valuable in the design of bioactive compounds and pharmaceuticals. Researchers appreciate its role in improving the solubility and stability of peptides, which is crucial for therapeutic applications.

In addition to its significance in peptide synthesis, Fmoc-L-2-amino-5-phenylpentanoic acid is also employed in the development of novel materials and bioconjugates. Its ability to form stable linkages with various biomolecules opens avenues for creating targeted drug delivery systems and diagnostic tools. The compound's compatibility with various coupling reagents and its ease of handling make it an essential choice for both academic and industrial laboratories focused on peptide chemistry and medicinal research.

Número CAS
959578-11-1
Fórmula molecular
C26H25NO4
Peso molecular
415.49
Número MDL
MFCD06202350
Rotación óptica
[a] D 20 = -10 ± 2º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
959578-11-1
Fórmula molecular
C26H25NO4
Peso molecular
415.49
Número MDL
MFCD06202350
Rotación óptica
[a] D 20 = -10 ± 2º (C=1 en DMF)
Condiciones
Conservar entre 0 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
-
Aplicaciones

Fmoc-L-2-amino-5-phenylpentanoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based pharmaceuticals, particularly in creating more stable and effective drug candidates for various therapeutic areas.
  • Bioconjugation: The compound is used in bioconjugation techniques, facilitating the attachment of peptides to other biomolecules, which is essential for developing targeted therapies and diagnostics.
  • Research in Neuroscience: Its derivatives are explored in neuroscience research for their potential neuroprotective effects, contributing to the development of treatments for neurodegenerative diseases.
  • Material Science: The compound is also investigated in the field of material science for creating novel biomaterials that mimic natural tissues, enhancing applications in regenerative medicine.

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