(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-fluorophenyl)butanoic acid
98%
- Product Code: 38367
CAS:
270596-49-1
| Molecular Weight: | 419.4500 g./mol | Molecular Formula: | C₂₅H₂₂FNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861009 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during the synthesis process. Its incorporation allows for the controlled assembly of peptides, particularly in solid-phase peptide synthesis (SPPS). The presence of the 2-fluorophenyl group can influence the peptide's biological activity or stability, making it valuable in the development of pharmaceuticals or bioactive peptides. Additionally, its structure is tailored for applications in medicinal chemistry, where it may be used to create analogs for drug discovery or to study structure-activity relationships.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $118.35 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(2-fluorophenyl)butanoic acid
This compound is primarily utilized in the field of peptide synthesis, where it serves as a protected amino acid derivative. The fluorenylmethoxycarbonyl (Fmoc) group acts as a protecting group for the amine functionality, ensuring selective reactions during the synthesis process. Its incorporation allows for the controlled assembly of peptides, particularly in solid-phase peptide synthesis (SPPS). The presence of the 2-fluorophenyl group can influence the peptide's biological activity or stability, making it valuable in the development of pharmaceuticals or bioactive peptides. Additionally, its structure is tailored for applications in medicinal chemistry, where it may be used to create analogs for drug discovery or to study structure-activity relationships.
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