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Catalog Number:
07220
CAS Number:
133373-24-7
Fmoc- N -metil- O - terc -butil-L-tirosina
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc -N -Me-L-Tyr(tBu)-OH
Documents
$72.31 /250 mg
Tamaño
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Información del producto

Fmoc-N-methyl-O-tert-butyl-L-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 amino groups during the synthesis of peptides. Its unique structure, including the tert-butyl and methyl groups, enhances solubility and stability, making it an ideal choice for researchers in organic chemistry and biochemistry.

In practical applications, Fmoc-N-methyl-O-tert-butyl-L-tyrosine is particularly valuable in the development of therapeutic peptides and proteins, where precise control over amino acid sequences is crucial. Its use in solid-phase peptide synthesis allows for efficient and high-yield production of complex peptides, which can be further explored for pharmaceutical applications. Researchers appreciate its compatibility with various coupling reagents and its ability to facilitate the synthesis of modified peptides, thus expanding the potential for innovative drug design and development.

Número CAS
133373-24-7
Fórmula molecular
C 29 H 31 N.º 5
Peso molecular
473.6
Número MDL
MFCD02684471
Punto de fusión
180 - 190 ºC
Rotación óptica
[a] D 20 = -49 ± 2 º (C=1 en DMF)
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
133373-24-7
Fórmula molecular
C 29 H 31 N.º 5
Peso molecular
473.6
Número MDL
MFCD02684471
Punto de fusión
180 - 190 ºC
Rotación óptica
[a] D 20 = -49 ± 2 º (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
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Aplicaciones

Fmoc-N-methyl-O-tert-butyl-L-tyrosine is widely utilized in research focused on:

  • Peptide Synthesis: This compound is a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis (SPPS). Its protective groups allow for selective reactions, facilitating the creation of complex peptide structures.
  • Drug Development: In pharmaceutical research, it is used to develop peptide-based drugs. Its stability and compatibility with various reaction conditions make it an ideal candidate for creating therapeutic peptides.
  • Bioconjugation: The compound can be employed in bioconjugation processes, where it helps attach peptides to other biomolecules, enhancing drug delivery systems and improving the efficacy of therapeutic agents.
  • Research in Neuroscience: It plays a role in synthesizing neuropeptides, which are crucial for studying neurological functions and disorders, providing insights into potential treatments for conditions like depression and anxiety.
  • Custom Peptide Libraries: Researchers utilize it to create diverse peptide libraries for screening and identifying new bioactive compounds, aiding in the discovery of novel therapeutics.

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