(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(3-cyanophenyl)butanoic acid
98%
- Product Code: 38368
CAS:
270065-87-7
| Molecular Weight: | 426.4600 g./mol | Molecular Formula: | C₂₆H₂₂N₂O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01861077 | |
| Melting Point: | Boiling Point: | 682.6 °C at 760 mmHg | |
| Density: | 1.33g/cm3 | Storage Condition: | -20°C |
Product Description:
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety for the amino group, ensuring selective reactions during peptide chain assembly. The presence of the cyano group on the phenyl ring can introduce specific structural or functional properties into the final peptide, such as enhanced binding affinity or stability. It is commonly employed in pharmaceutical research and development for creating peptide-based drugs, biomaterials, and probes for biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,048.00 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(3-cyanophenyl)butanoic acid
This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing peptides, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective moiety for the amino group, ensuring selective reactions during peptide chain assembly. The presence of the cyano group on the phenyl ring can introduce specific structural or functional properties into the final peptide, such as enhanced binding affinity or stability. It is commonly employed in pharmaceutical research and development for creating peptide-based drugs, biomaterials, and probes for biochemical studies.
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