(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-oxo-4-(tritylamino)butanoic acid
97%
- Product Code: 37417
CAS:
2044711-09-1
| Molecular Weight: | 610.7000 g./mol | Molecular Formula: | C₃₉H₃₄N₂O₅ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino function, and the trityl (Trt) group protects the side chain amino group. This dual protection strategy is crucial for the stepwise construction of peptides, ensuring that specific amino acids are added in the correct sequence without unwanted side reactions. The compound is especially valuable in the synthesis of complex peptides and proteins, where precise control over the assembly process is required. Its application extends to pharmaceutical research and development, where it aids in the production of peptide-based drugs and bioactive compounds. Additionally, it is used in biochemical studies to investigate protein structure and function, as well as in the development of peptide-based diagnostics and therapeutics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $448.42 |
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(R)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(methyl)amino)-4-oxo-4-(tritylamino)butanoic acid
This chemical is primarily utilized in the field of peptide synthesis, particularly in solid-phase peptide synthesis (SPPS). It serves as a protected amino acid derivative, where the fluorenylmethoxycarbonyl (Fmoc) group acts as a temporary protecting group for the amino function, and the trityl (Trt) group protects the side chain amino group. This dual protection strategy is crucial for the stepwise construction of peptides, ensuring that specific amino acids are added in the correct sequence without unwanted side reactions. The compound is especially valuable in the synthesis of complex peptides and proteins, where precise control over the assembly process is required. Its application extends to pharmaceutical research and development, where it aids in the production of peptide-based drugs and bioactive compounds. Additionally, it is used in biochemical studies to investigate protein structure and function, as well as in the development of peptide-based diagnostics and therapeutics.
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