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Catalog Number:
03235
CAS Number:
187526-99-4
Fmoc -O - tert -butil-L-tirosinol
Purity:
≥ 98 % (HPLC)
Synonym(s):
Fmoc-L-tirosinol(tBu), Fmoc-Tyr(tBu)-ol
Documents
$141.41 /1G
Tamaño
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Información del producto

Fmoc-O-tert-butyl-L-tyrosinol is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This protected amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) group, which provides stability during synthesis while allowing for easy deprotection when needed. Its unique structure, characterized by the tert-butyl and hydroxy groups, enhances solubility and reactivity, making it an ideal choice for researchers focused on developing complex peptides and pharmaceuticals.

In practical applications, Fmoc-O-tert-butyl-L-tyrosinol is particularly valuable in the synthesis of bioactive peptides, which are crucial in drug development and therapeutic research. Its ability to facilitate the formation of peptide bonds while maintaining the integrity of sensitive functional groups makes it a preferred reagent in combinatorial chemistry and high-throughput screening. Researchers benefit from its high purity and reliable performance, ensuring consistent results in their experiments and formulations.

Número CAS
187526-99-4
Fórmula molecular
C 28 H 31 N.º 4
Peso molecular
445.5
Número MDL
MFCD00235959
Punto de fusión
~ 120 ºC
Rotación óptica
[a] 20 D = - 42 ± 3º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
187526-99-4
Fórmula molecular
C 28 H 31 N.º 4
Peso molecular
445.5
Número MDL
MFCD00235959
Punto de fusión
~ 120 ºC
Rotación óptica
[a] 20 D = - 42 ± 3º (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-tert-butyl-L-tyrosinol is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing researchers to selectively modify amino acids without affecting others. Its stability under various conditions makes it a preferred choice in organic synthesis.
  • Drug Development: In pharmaceutical research, it plays a crucial role in the design of new drugs, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Material Science: It finds applications in the creation of advanced materials, such as polymers and nanomaterials, which can be tailored for specific properties in electronics or biomedical devices.
  • Research in Neuroscience: Researchers utilize this compound to study neurotransmitter systems and receptor interactions, contributing to the understanding of various neurological conditions.

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