(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(pyridin-3-yl)propanoic acid

95%

  • Product Code: 104242
  CAS:    511272-43-8
Molecular Weight: 388.42 g./mol Molecular Formula: C₂₃H₂₀N₂O₄
EC Number: MDL Number: MFCD03428024
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This chemical is primarily used in the field of peptide synthesis, where it serves as a building block for the creation of complex peptide structures. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the fluorenylmethoxycarbonyl (Fmoc) protecting group, which can be easily removed under mild basic conditions without affecting other functional groups in the peptide chain. The pyridine moiety in its structure can also play a role in enhancing solubility and facilitating purification processes. Additionally, it is utilized in the development of pharmaceuticals and bioactive compounds, especially those targeting specific receptors or enzymes where the pyridine group may contribute to binding affinity or activity. Its application extends to research in drug discovery and the synthesis of peptide-based therapeutics.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿6,588.00
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0.250 10-20 days ฿9,900.00
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1.000 10-20 days ฿24,750.00
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(pyridin-3-yl)propanoic acid
This chemical is primarily used in the field of peptide synthesis, where it serves as a building block for the creation of complex peptide structures. It is particularly valuable in solid-phase peptide synthesis (SPPS) due to the presence of the fluorenylmethoxycarbonyl (Fmoc) protecting group, which can be easily removed under mild basic conditions without affecting other functional groups in the peptide chain. The pyridine moiety in its structure can also play a role in enhancing solubility and facilitating purification processes. Additionally, it is utilized in the development of pharmaceuticals and bioactive compounds, especially those targeting specific receptors or enzymes where the pyridine group may contribute to binding affinity or activity. Its application extends to research in drug discovery and the synthesis of peptide-based therapeutics.
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