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Catalog Number:
15450
CAS Number:
479064-95-4
Acide Fmoc-( R -3-amino-3-(4-fluorophényl)propionique
Purity:
≥ 99 % (pureté chirale)
Synonym(s):
Fmoc-D-β-Phe(4-F)-OH, ( R -Fmoc-4-fluoro-β-phénylalanine
Documents
$72.31 /250 mg
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Product Information

Fmoc-(R)-3-amino-3-(4-fluorophenyl)propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorophenyl group that enhances its bioactivity, making it particularly valuable in the design of pharmaceuticals targeting specific biological pathways. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex peptides with high purity and yield. Researchers appreciate its stability under various conditions, which supports its use in both academic and industrial settings.

In addition to its application in peptide synthesis, Fmoc-(R)-3-amino-3-(4-fluorophenyl)propionic acid can serve as a key intermediate in the development of novel therapeutics, particularly in the fields of oncology and neurology. Its unique structural features enable the exploration of new drug candidates with improved efficacy and selectivity. This compound stands out among similar products due to its enhanced solubility and reactivity, making it an ideal choice for researchers looking to innovate in peptide-based drug design.

Synonyms
Fmoc-D-β-Phe(4-F)-OH, ( R -Fmoc-4-fluoro-β-phénylalanine
CAS Number
479064-95-4
Purity
≥ 99 % (pureté chirale)
Molecular Formula
C 24 H 20 FNO 4
Molecular Weight
405.42
MDL Number
MFCD03428033
PubChem ID
2759194
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-D-β-Phe(4-F)-OH, ( R -Fmoc-4-fluoro-β-phénylalanine
CAS Number
479064-95-4
Purity
≥ 99 % (pureté chirale)
Molecular Formula
C 24 H 20 FNO 4
Molecular Weight
405.42
MDL Number
MFCD03428033
PubChem ID
2759194
Appearance
Poudre blanche
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-(4-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, where its Fmoc protecting group allows for easy removal and reactivity control.
  • Drug Development: Its unique structure makes it valuable in the design of pharmaceuticals, especially for targeting specific receptors in the treatment of various diseases, including cancer and neurological disorders.
  • Bioconjugation: The compound can be used in bioconjugation processes, linking biomolecules to drugs or imaging agents, enhancing the specificity and efficacy of therapeutic agents.
  • Research in Neuroscience: Due to its structural similarity to neurotransmitters, it is employed in studies related to neuropharmacology, helping researchers understand receptor interactions and drug effects.
  • Material Science: This chemical is also explored in the development of novel materials, such as polymers and hydrogels, which can be used in drug delivery systems or tissue engineering applications.

Citations