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Catalog Number:
15642
CAS Number:
501015-29-8
Ácido Fmoc-( S -3-amino-3-(3-metoxifenil)propiónico
Purity:
≥ 95 % (HPLC)
Synonym(s):
Fmoc-L-β-Phe(3-OMe)-OH, ( S -Fmoc-3-metoxi-β-fenilalanina
Documents
$86.23 /250 mg
Tamaño
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Product Information

Fmoc-(S)-3-amino-3-(3-methoxyphenyl)propionic acid is a valuable compound widely utilized in the field of peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amines during the synthesis of peptides. Its unique structure not only enhances the stability of the compound but also facilitates the introduction of complex functionalities in peptide chains. Researchers and industry professionals appreciate its application in the synthesis of bioactive peptides and pharmaceuticals, particularly in the development of targeted therapies and drug candidates.

The compound's ability to provide a robust and versatile platform for peptide synthesis makes it a preferred choice among chemists. Its compatibility with various coupling reagents and solid-phase synthesis techniques allows for efficient and high-yield production of peptides. Additionally, the presence of the methoxyphenyl group contributes to the compound's hydrophobic characteristics, which can improve the solubility and bioavailability of the resulting peptides. This makes Fmoc-(S)-3-amino-3-(3-methoxyphenyl)propionic acid an essential tool for researchers aiming to explore new therapeutic avenues.

Synonyms
Fmoc-L-β-Phe(3-OMe)-OH, ( S -Fmoc-3-metoxi-β-fenilalanina
CAS Number
501015-29-8
Purity
≥ 95 % (HPLC)
Molecular Formula
C 25 H 23 N º 5
Molecular Weight
417.46
MDL Number
MFCD03427975
PubChem ID
2759197
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-β-Phe(3-OMe)-OH, ( S -Fmoc-3-metoxi-β-fenilalanina
CAS Number
501015-29-8
Purity
≥ 95 % (HPLC)
Molecular Formula
C 25 H 23 N º 5
Molecular Weight
417.46
MDL Number
MFCD03427975
PubChem ID
2759197
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(S)-3-amino-3-(3-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 (SPPS), allowing researchers to create complex peptide sequences efficiently.
  • Drug Development: It is used in the design of peptide-based drugs, especially in targeting specific receptors, which can lead to more effective treatments with fewer side effects compared to traditional small-molecule drugs.
  • Bioconjugation: The chemical's functional groups facilitate bioconjugation processes, enabling the attachment of biomolecules to surfaces or other compounds, which is essential in developing biosensors and drug delivery systems.
  • Research in Neuroscience: Its structural properties make it valuable in studying neuropeptides, contributing to the understanding of neurological functions and potential therapies for neurodegenerative diseases.
  • Material Science: This compound can be incorporated into polymer matrices to develop smart materials with specific properties, such as enhanced biocompatibility for medical implants.

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