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Catalog Number:
03638
CAS Number:
144120-53-6
Éster a-alílico del ácido fmoc-L-aspártico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-Asp-OAll
Documents
$58.39 /1G
Tamaño
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Información del producto

Fmoc-L-aspartic acid a-allyl ester is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This derivative of aspartic acid features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino acids during the synthesis of peptides. Its unique structure allows for efficient coupling reactions, making it an ideal choice for researchers focusing on the development of bioactive peptides and pharmaceuticals. The allyl ester functionality enhances its reactivity, facilitating further modifications and applications in organic synthesis.

In addition to its role in peptide synthesis, Fmoc-L-aspartic acid a-allyl ester has potential applications in the development of drug delivery systems and biomaterials. Its ability to form stable linkages and its compatibility with various coupling agents make it a valuable tool for chemists and researchers aiming to create innovative therapeutic agents. By choosing this compound, professionals can streamline their synthesis processes and enhance the efficacy of their research projects.

Número CAS
144120-53-6
Fórmula molecular
C22H21NO6
Peso molecular
395.4
Número MDL
MFCD00467715
Punto de fusión
119-125 ?C
Rotación óptica
[a] D 20 = -24 ± 3º (C=1 en DMF)
Condiciones
Conservar a ≤ -18 °C
Información general
Número CAS
144120-53-6
Fórmula molecular
C22H21NO6
Peso molecular
395.4
Número MDL
MFCD00467715
Punto de fusión
119-125 ?C
Rotación óptica
[a] D 20 = -24 ± 3º (C=1 en DMF)
Condiciones
Conservar a ≤ -18 °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-aspartic acid a-allyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound is commonly used as a building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, due to its protective Fmoc group that allows for selective deprotection.
  • Drug Development: It plays a crucial role in the development of peptide-based drugs, facilitating the creation of compounds with enhanced bioactivity and stability, which is vital for pharmaceutical applications.
  • Bioconjugation: The allyl ester functionality enables efficient bioconjugation reactions, making it valuable in the creation of targeted drug delivery systems and diagnostic agents in the biomedical field.
  • Research in Neuroscience: This compound is used in studies related to neurotransmitter pathways, particularly in the synthesis of aspartate derivatives that can help in understanding brain functions and disorders.
  • Polymer Chemistry: It is utilized in the development of novel polymers with specific functionalities, which can be applied in various industries, including materials science and nanotechnology.

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