(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-(tert-butoxy)phenyl)propanoic acid
98%
- Product Code: 37413
CAS:
1799443-50-7
| Molecular Weight: | 473.5600 g./mol | Molecular Formula: | C₂₉H₃₁NO₅ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized 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 temporary protecting group for the amino functionality, allowing selective deprotection during the synthesis process. The tert-butoxy group on the phenyl ring provides additional protection for the side chain, ensuring stability during peptide elongation. Its application is critical in the production of peptides for pharmaceutical research, drug development, and biochemical studies, enabling the creation of complex peptide structures with high precision.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | Ft34,035.41 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-3-(4-(tert-butoxy)phenyl)propanoic acid
This compound is primarily utilized 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 temporary protecting group for the amino functionality, allowing selective deprotection during the synthesis process. The tert-butoxy group on the phenyl ring provides additional protection for the side chain, ensuring stability during peptide elongation. Its application is critical in the production of peptides for pharmaceutical research, drug development, and biochemical studies, enabling the creation of complex peptide structures with high precision.
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