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Catalog Number:
15547
CAS Number:
511272-51-8
Ácido Fmoc-( R -3-amino-3-(3-fluorofenil)propiónico
Synonym(s):
Fmoc-D-β-Phe(3-F)-OH, ( R -Fmoc-3-fluoro-β-fenilalanina
Documents
$206.60 /1G
Tamaño
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Product Information

Fmoc-(R)-3-amino-3-(3-fluorophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a fluorinated aromatic group, which enhances its biological activity and selectivity, making it an ideal candidate for the development of novel therapeutics. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into peptide chains while providing stability during synthesis. Researchers appreciate its role in the production of peptides that target specific biological pathways, particularly in the fields of drug discovery and development.

The unique properties of Fmoc-(R)-3-amino-3-(3-fluorophenyl)propionic acid make it particularly valuable in the synthesis of bioactive compounds, including those with potential applications in cancer treatment and neuropharmacology. Its ability to facilitate the introduction of fluorine into peptide structures can lead to enhanced pharmacokinetic profiles and improved binding affinities. This compound is essential for professionals looking to innovate in peptide-based therapies and expand their research capabilities.

Synonyms
Fmoc-D-β-Phe(3-F)-OH, ( R -Fmoc-3-fluoro-β-fenilalanina
CAS Number
511272-51-8
Molecular Formula
C 24 H 20 FNO 4
Molecular Weight
405.42
MDL Number
MFCD03428032
PubChem ID
2759193
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-β-Phe(3-F)-OH, ( R -Fmoc-3-fluoro-β-fenilalanina
CAS Number
511272-51-8
Molecular Formula
C 24 H 20 FNO 4
Molecular Weight
405.42
MDL Number
MFCD03428032
PubChem ID
2759193
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-(3-fluorophenyl)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). Its Fmoc protecting group allows for easy deprotection, making it ideal for creating complex peptide sequences.
  • Drug Development: The unique structural properties enable researchers to explore new therapeutic agents, particularly in the field of oncology and neurology, where modifications can lead to improved drug efficacy and specificity.
  • Bioconjugation: It is used in bioconjugation processes, where it can be linked to various biomolecules, enhancing the targeting capabilities of drugs or imaging agents in medical applications.
  • Research in Neuroscience: The compound's fluorophenyl group is valuable in studying neuroactive peptides, contributing to the understanding of neurotransmitter systems and potential treatments for neurological disorders.
  • Material Science: Its properties are explored in the development of novel materials, such as hydrogels and polymers, which can be used in drug delivery systems or tissue engineering applications.

Citas