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Catalog Number:
15678
CAS Number:
511272-39-2
Fmoc-(R-3-amino-3-(2,3-dimethoxyphenyl)propionic acid
Synonym(s):
Fmoc-D-β-Phe(2,3-dimethoxy)-OH, (R-Fmoc-2,3-dimethoxy-β-phenylalanine
Documents
$206.60 /1G
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Product Information

Fmoc-(R)-3-amino-3-(2,3-dimethoxyphenyl)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 2,3-dimethoxyphenyl group, enhances its reactivity and compatibility with various coupling reagents, making it an excellent choice for researchers focused on developing complex peptide sequences.

In addition to its role in peptide synthesis, this compound has potential applications in drug discovery and development, particularly in the design of bioactive peptides and pharmaceuticals. Its ability to facilitate the formation of stable peptide bonds while maintaining the integrity of the amino acid side chains allows for the creation of diverse peptide libraries. Researchers can leverage Fmoc-(R)-3-amino-3-(2,3-dimethoxyphenyl)propionic acid to explore new therapeutic avenues, particularly in the fields of oncology and neurology, where peptide-based therapies are gaining traction.

Synonyms
Fmoc-D-β-Phe(2,3-dimethoxy)-OH, (R-Fmoc-2,3-dimethoxy-β-phenylalanine
CAS Number
511272-39-2
Molecular Formula
C26H25NO6
Molecular Weight
447.49
MDL Number
MFCD03428020
PubChem ID
22309349
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-D-β-Phe(2,3-dimethoxy)-OH, (R-Fmoc-2,3-dimethoxy-β-phenylalanine
CAS Number
511272-39-2
Molecular Formula
C26H25NO6
Molecular Weight
447.49
MDL Number
MFCD03428020
PubChem ID
22309349
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R)-3-amino-3-(2,3-dimethoxyphenyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, enhancing the efficiency of creating complex peptides with specific sequences.
  • Drug Development: Its application in medicinal chemistry allows researchers to design and optimize drug candidates, particularly in developing compounds targeting specific receptors.
  • Bioconjugation: The compound is used to create bioconjugates, linking biomolecules for targeted drug delivery systems, which can improve therapeutic efficacy and reduce side effects.
  • Research in Neuroscience: It plays a role in studying neuroactive compounds, helping researchers understand the interactions between peptides and neurotransmitter systems.
  • Material Science: The compound can be incorporated into polymeric materials, enhancing their properties for applications in drug delivery and tissue engineering.

Citations