(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(7-fluoro-1H-indol-3-yl)propanoic acid

95%

  • Product Code: 38029
  CAS:    1956434-65-3
Molecular Weight: 444.45 g./mol Molecular Formula: C₂₆H₂₁FN₂O₄
EC Number: MDL Number: MFCD26960591
Melting Point: Boiling Point: 713.9±60.0°C at 760 mmHg
Density: Storage Condition: 2-8°C, dry and sealed
Product Description: This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. The fluoroindole moiety makes it valuable in the synthesis of peptides with specific biological activities, especially those targeting receptor binding or enzyme inhibition. Its application is crucial in the development of pharmaceuticals, including drug candidates for neurological disorders, cancer, and other diseases where indole derivatives play a significant role. Additionally, it is utilized in research to study peptide structure-activity relationships and to create peptide-based probes for biochemical assays.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿12,168.00
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0.250 10-20 days ฿24,336.00
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(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(7-fluoro-1H-indol-3-yl)propanoic acid
This compound is primarily used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality. The fluoroindole moiety makes it valuable in the synthesis of peptides with specific biological activities, especially those targeting receptor binding or enzyme inhibition. Its application is crucial in the development of pharmaceuticals, including drug candidates for neurological disorders, cancer, and other diseases where indole derivatives play a significant role. Additionally, it is utilized in research to study peptide structure-activity relationships and to create peptide-based probes for biochemical assays.
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