(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-nitrophenyl)butanoic acid
≥95%
- Product Code: 37759
CAS:
269398-78-9
| Molecular Weight: | 446.45 g./mol | Molecular Formula: | C₂₅H₂₂N₂O₆ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01860920 | |
| Melting Point: | Boiling Point: | 703.4°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
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 with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amine functionality, ensuring selective reactions during peptide chain elongation. The nitro group on the phenyl ring can be utilized for further chemical modifications or as a handle for conjugation in bioconjugation chemistry. Its application is significant in pharmaceutical research, where it aids in the development of peptide-based drugs, bioactive peptides, and peptidomimetics. Additionally, it is employed in the study of enzyme-substrate interactions and protein engineering.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $70.07 |
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| 0.100 | 10-20 days | $112.10 |
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| 0.250 | 10-20 days | $179.46 |
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(R)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(4-nitrophenyl)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 with specific sequences, particularly in solid-phase peptide synthesis (SPPS). The fluorenylmethoxycarbonyl (Fmoc) group acts as a protective group for the amine functionality, ensuring selective reactions during peptide chain elongation. The nitro group on the phenyl ring can be utilized for further chemical modifications or as a handle for conjugation in bioconjugation chemistry. Its application is significant in pharmaceutical research, where it aids in the development of peptide-based drugs, bioactive peptides, and peptidomimetics. Additionally, it is employed in the study of enzyme-substrate interactions and protein engineering.
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