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Catalog Number:
05688
CAS Number:
214852-39-8
Éster β-2-fenilisopropílico del ácido Fmoc-D-aspártico
Purity:
≥ 99,8 % (HPLC quiral)
Synonym(s):
Fmoc-D-Asp(2-fenilisopropiloxi)-OH
Documents
$185.40 /100 mg
Tamaño
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Información del producto

Fmoc-D-aspartic acid b-2-phenylisopropyl ester is a versatile compound widely utilized in peptide synthesis and drug development. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability and ease of handling during the synthesis process. Its unique structure allows for selective reactions, making it an essential building block in the creation of complex peptides and proteins. Researchers in the fields of biochemistry and pharmaceuticals often leverage this compound for its ability to enhance solubility and improve the overall yield of peptide synthesis.

Additionally, Fmoc-D-aspartic acid b-2-phenylisopropyl ester is particularly valuable in the development of therapeutic agents targeting neurological disorders, given its structural similarity to naturally occurring amino acids. Its application in solid-phase peptide synthesis (SPPS) allows for the efficient assembly of peptides with high purity, making it a preferred choice among professionals in drug discovery and development. With its reliable performance and adaptability, this compound stands out as a key player in advancing research and innovation in the pharmaceutical industry.

Número CAS
214852-39-8
Fórmula molecular
C 28 H 27 N º 6
Peso molecular
473.53
Número MDL
MFCD01632049
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
214852-39-8
Fórmula molecular
C 28 H 27 N º 6
Peso molecular
473.53
Número MDL
MFCD01632049
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-D-aspartic acid b-2-phenylisopropyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions without interfering with other functional groups. Its stability under various conditions makes it a preferred choice for researchers in organic chemistry.
  • Drug Development: In pharmaceutical research, it is used to create modified amino acids that can enhance the efficacy of drug candidates. This can lead to improved therapeutic profiles and reduced side effects in drug formulations.
  • Bioconjugation: The compound can be employed in bioconjugation processes, where it helps in attaching biomolecules to surfaces or other molecules, facilitating the development of targeted therapies and diagnostic tools.
  • Protein Engineering: Researchers utilize it to modify proteins, enhancing their stability and functionality. This application is crucial in developing enzymes and antibodies with improved characteristics for industrial and medical use.
  • Research in Neuroscience: Its derivatives are explored in studies related to neurotransmitter pathways, aiding in the understanding of neurological disorders and the development of potential treatments.

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