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Catalog Number:
07048
CAS Number:
221884-63-5
Fmoc-a-alil-DL-glicina
Purity:
≥ 99%
Synonym(s):
Fmoc-DL-Gly(α-alil)-OH, Ácido fmoc-DL-2-amino-4-pentenoico
Documents
$72.31 /250 mg
Tamaño
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Información del producto

Fmoc-a-allyl-DL-glycine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethyloxycarbonyl) group, which facilitates the selective modification of amino acids during solid-phase peptide synthesis. Its unique allyl side chain enhances the compound's reactivity, making it an excellent choice for researchers looking to introduce specific functionalities into peptides.

In addition to its role in peptide synthesis, Fmoc-a-allyl-DL-glycine can be employed in the development of novel therapeutic agents, particularly in the fields of medicinal chemistry and biochemistry. Its ability to undergo various coupling reactions allows for the creation of complex peptide structures, which are essential in the design of biologically active compounds. Researchers benefit from its stability and compatibility with a range of coupling reagents, making it a valuable tool in the synthesis of custom peptides for pharmaceutical applications.

Número CAS
221884-63-5
Fórmula molecular
C 20 H 19 N.º 4
Peso molecular
337.42
Número MDL
MFCD02259489
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
221884-63-5
Fórmula molecular
C 20 H 19 N.º 4
Peso molecular
337.42
Número MDL
MFCD02259489
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-a-allyl-DL-glycine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, allowing for the incorporation of unique functionalities that enhance peptide properties.
  • Drug Development: Its structural characteristics make it valuable in the design of novel pharmaceuticals, especially in creating compounds with improved bioactivity and selectivity.
  • Bioconjugation: The allyl group facilitates bioconjugation reactions, enabling researchers to attach biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Research in Neuroscience: It can be used to study neuropeptides and their interactions, contributing to advancements in understanding neurological disorders and potential treatments.
  • Material Science: The compound's unique properties allow it to be used in developing advanced materials, such as hydrogels, which can be applied in tissue engineering and regenerative medicine.

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