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Catalog Number:
15645
CAS Number:
511272-33-6
Ácido Fmoc-( R -3-amino-3-(4-metoxifenil)propiónico
Synonym(s):
Fmoc-D-β-Phe(4-OMe)-OH, ( R -Fmoc-4-metoxi-β-fenilalanina
Documents
$206.60 /1G
Tamaño
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Product Information

Fmoc-(R)-3-amino-3-(4-methoxyphenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. 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, characterized by the presence of a methoxyphenyl group, enhances its solubility and stability, making it an ideal choice for researchers looking to develop complex peptide sequences.

In practical applications, this compound is particularly valuable in the pharmaceutical industry for the development of bioactive peptides and drug candidates. Its ability to facilitate the synthesis of peptides with specific biological activities allows researchers to explore new therapeutic avenues. Additionally, Fmoc-(R)-3-amino-3-(4-methoxyphenyl)propionic acid can be employed in the creation of peptide-based materials and biomaterials, further expanding its utility in various fields, including drug delivery and tissue engineering.

Synonyms
Fmoc-D-β-Phe(4-OMe)-OH, ( R -Fmoc-4-metoxi-β-fenilalanina
CAS Number
511272-33-6
Molecular Formula
C 25 H 23 N º 5
Molecular Weight
417.46
MDL Number
MFCD03428014
PubChem ID
2759198
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-β-Phe(4-OMe)-OH, ( R -Fmoc-4-metoxi-β-fenilalanina
CAS Number
511272-33-6
Molecular Formula
C 25 H 23 N º 5
Molecular Weight
417.46
MDL Number
MFCD03428014
PubChem ID
2759198
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(4-methoxyphenyl)propionic acid 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 efficient assembly of complex peptide sequences.
  • Drug Development: It is used in the design of pharmaceuticals, especially in creating compounds that target specific biological pathways, enhancing the efficacy of drug candidates.
  • Bioconjugation: The chemical's functional groups facilitate bioconjugation processes, enabling the attachment of biomolecules to surfaces or other compounds, which is crucial in developing targeted therapies.
  • Research in Neuroscience: Its application in synthesizing neuropeptides aids in studying neurological functions and disorders, providing insights into potential treatments for conditions like depression or anxiety.
  • Material Science: The compound is explored for its properties in creating novel materials, such as hydrogels, which can be used in drug delivery systems or tissue engineering applications.

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