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Catalog Number:
12394
CAS Number:
204269-35-2
Fmoc -O -alil-D-tirosina
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-D-Tyr(Todo)-OH
Documents
$36.65 /1G
Tamaño
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Información del producto

Fmoc-O-allyl-D-tyrosine is a versatile amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis process. Its unique allyl side chain enhances its reactivity and provides additional functionalization options, making it an excellent choice for researchers focused on developing complex peptides and biologically active compounds.

In the pharmaceutical industry, Fmoc-O-allyl-D-tyrosine is particularly valuable for its role in the synthesis of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its properties allow for efficient coupling reactions, leading to higher yields and purities in peptide synthesis. Additionally, the compound's structural features enable its use in various applications, including the development of enzyme inhibitors and targeted drug delivery systems. Researchers will find that Fmoc-O-allyl-D-tyrosine not only simplifies the synthesis process but also enhances the overall efficiency of their projects.

Número CAS
204269-35-2
Fórmula molecular
C27H25Nº 5
Peso molecular
443.5
Número MDL
MFCD01074692
Punto de fusión
145-155 °C
Rotación óptica
[a] D 20 = +22,0 a +25,0º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
204269-35-2
Fórmula molecular
C27H25Nº 5
Peso molecular
443.5
Número MDL
MFCD01074692
Punto de fusión
145-155 °C
Rotación óptica
[a] D 20 = +22,0 a +25,0º (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-O-allyl-D-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex structures with specific functionalities.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new drugs, particularly those targeting specific receptors or pathways.
  • Bioconjugation: The allyl group allows for selective reactions, making it useful in bioconjugation processes where precise attachment of biomolecules is required.
  • Research in Neuroscience: This compound can be used in studies related to neurotransmitter functions, aiding in the understanding of various neurological conditions.
  • Material Science: Its chemical properties lend themselves to applications in creating novel materials, particularly in the development of smart polymers.

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