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Catalog Number:
16844
CAS Number:
959580-94-0
Ácido Fmoc-( S -3-amino-4-(2,4,5-trifluorofenil)butírico
Documents
$113.87 /25 mg
Tamaño
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Product Information

Fmoc-(S)-3-amino-4-(2,4,5-trifluorophenyl)butyric acid is a specialized amino acid derivative widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (9-fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its trifluorophenyl moiety enhances the compound's hydrophobic character, making it particularly valuable in the design of bioactive peptides and pharmaceuticals. Researchers appreciate its ability to facilitate the formation of stable peptide bonds while maintaining the integrity of sensitive functional groups.

In practical applications, Fmoc-(S)-3-amino-4-(2,4,5-trifluorophenyl)butyric acid is instrumental in the development of therapeutic peptides, especially those targeting specific receptors or enzymes. Its unique structure allows for the fine-tuning of peptide properties, which is crucial in optimizing drug efficacy and selectivity. This compound stands out in the field of medicinal chemistry for its versatility and effectiveness in producing high-purity peptides, making it a preferred choice for researchers and industry professionals alike.

CAS Number
959580-94-0
Molecular Formula
C25H20F3NO4
Molecular Weight
455.43
MDL Number
MFCD06659151
PubChem ID
53398431
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
959580-94-0
Molecular Formula
C25H20F3NO4
Molecular Weight
455.43
MDL Number
MFCD06659151
PubChem ID
53398431
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-4-(2,4,5-trifluorophenyl)butyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a crucial building block in solid-phase peptide synthesis, allowing researchers to create complex peptides with high purity and yield.
  • Drug Development: Its unique structure and properties make it valuable in the pharmaceutical industry for developing novel drugs, particularly in targeting specific biological pathways.
  • Bioconjugation: The chemical's functional groups facilitate bioconjugation processes, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Research in Neuroscience: Due to its potential effects on neurotransmitter systems, this compound is used in studies exploring neuropharmacology and the development of treatments for neurological disorders.
  • Fluorinated Compound Studies: Its trifluorophenyl group allows for the investigation of fluorinated compounds, which are important in materials science and medicinal chemistry for enhancing bioactivity and stability.

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