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Catalog Number:
16693
CAS Number:
959583-03-0
Fmoc-(2S,3S-3-amino-3-(4-fluorophenyl)-2-hydroxypropionic acid
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$201.00 /100MG
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Product Information

Fmoc-(2S,3S)-3-amino-3-(4-fluorophenyl)-2-hydroxypropionic acid is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This amino acid derivative features a fluorinated aromatic side chain, enhancing its biological activity and selectivity in various applications. The Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into peptide sequences, making it an essential building block for researchers focused on developing novel therapeutics and biologically active peptides.

In addition to its role in peptide synthesis, this compound's unique structure may contribute to improved binding affinities in drug design, particularly in targeting specific receptors or enzymes. Its potential applications extend to the development of inhibitors or modulators in pharmaceutical research, where precision and efficacy are paramount. Researchers can leverage the properties of Fmoc-(2S,3S)-3-amino-3-(4-fluorophenyl)-2-hydroxypropionic acid to create innovative solutions in drug discovery and development, making it a valuable addition to any laboratory focused on cutting-edge research.

CAS Number
959583-03-0
Molecular Formula
C24H20FNO5
Molecular Weight
421.42
MDL Number
MFCD07363525
PubChem ID
53398437
Conditions
Store at 0-8°C
General Information
CAS Number
959583-03-0
Molecular Formula
C24H20FNO5
Molecular Weight
421.42
MDL Number
MFCD07363525
PubChem ID
53398437
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-(2S,3S)-3-amino-3-(4-fluorophenyl)-2-hydroxypropionic 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), allowing for the creation of complex peptide structures with high purity.
  • Drug Development: Its unique properties make it valuable in pharmaceutical research, especially for developing new drugs targeting specific biological pathways, enhancing efficacy and selectivity.
  • Bioconjugation: The chemical is used in bioconjugation processes, linking biomolecules to create targeted therapies or diagnostic agents, improving the precision of treatments in areas like cancer therapy.
  • Research in Neuroscience: It plays a role in studying neuroactive peptides, contributing to the understanding of neurological disorders and potential therapeutic interventions.
  • Fluorinated Compound Applications: The presence of fluorine enhances the compound's metabolic stability, making it suitable for applications in medicinal chemistry where stability is crucial for drug performance.

Citations