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Catalog Number:
15742
CAS Number:
959581-71-6
Acide Fmoc-( R -3-amino-3-(6-méthoxy-3-pyridyl)propionique
Synonym(s):
Fmoc-D-β-Ala-(6-méthoxy-3-pyridyl)-OH
Documents
$145.00 /100 mg
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Product Information

Fmoc-(R)-3-amino-3-(6-methoxy-3-pyridyl)propionic acid is a valuable compound widely utilized in peptide synthesis and drug development. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amine functionalities during the synthesis of complex peptides. Its unique structure, incorporating a 6-methoxy-3-pyridyl moiety, enhances its bioactivity and solubility, making it an attractive choice for researchers in medicinal chemistry and pharmaceutical applications.

This compound is particularly beneficial in the development of peptide-based therapeutics, where precise control over amino acid sequences is crucial. Its application extends to the synthesis of bioactive peptides, which can be used in various fields, including oncology and neurology. The ability to easily incorporate this compound into peptide chains allows for the exploration of novel therapeutic agents with improved efficacy and reduced side effects. Researchers and industry professionals will find Fmoc-(R)-3-amino-3-(6-methoxy-3-pyridyl)propionic acid to be an indispensable tool in advancing their projects.

Synonyms
Fmoc-D-β-Ala-(6-méthoxy-3-pyridyl)-OH
CAS Number
959581-71-6
Molecular Formula
C24H22N2O5
Molecular Weight
418.45
MDL Number
MFCD04118076
PubChem ID
53398102
Conditions
Conserver à 0-8°C
General Information
Synonyms
Fmoc-D-β-Ala-(6-méthoxy-3-pyridyl)-OH
CAS Number
959581-71-6
Molecular Formula
C24H22N2O5
Molecular Weight
418.45
MDL Number
MFCD04118076
PubChem ID
53398102
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(6-methoxy-3-pyridyl)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 the solid-phase peptide synthesis (SPPS) method, allowing for the creation of complex peptide structures.
  • Drug Development: Its unique properties make it valuable in medicinal chemistry for designing new pharmaceuticals, especially those targeting neurological disorders, due to its pyridine moiety which can enhance bioactivity.
  • Bioconjugation: The compound can be used in bioconjugation techniques, where it helps in attaching biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Research in Neuroscience: Its structural characteristics allow researchers to explore its effects on neurotransmitter systems, making it a useful tool in studying neuropharmacology.
  • Analytical Chemistry: It can be employed as a reference standard in various analytical techniques, aiding in the quantification and characterization of related compounds in research settings.

Citations