(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((4-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl)amino)benzyl)oxy)-4-oxobutanoic acid
98%
- Product Code: 38366
CAS:
172611-77-7
| Molecular Weight: | 666.7600 g./mol | Molecular Formula: | C₃₉H₄₂N₂O₈ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino functionality during the synthesis process, ensuring selective reactions at other sites. The compound's structure also includes a labile linker, which allows for the controlled release of the peptide from the solid support after synthesis. Its application is crucial in the production of complex peptides and proteins, enabling high purity and efficiency in biotechnological and pharmaceutical research. Additionally, it is employed in the development of peptide-based drugs and bioactive molecules due to its stability and compatibility with various synthetic protocols.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft33,550.57 |
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(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-((4-((1-(4,4-dimethyl-2,6-dioxocyclohexylidene)-3-methylbutyl)amino)benzyl)oxy)-4-oxobutanoic acid
This compound is primarily utilized in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) as a protecting group for amino acids. The fluorenylmethoxycarbonyl (Fmoc) group protects the amino functionality during the synthesis process, ensuring selective reactions at other sites. The compound's structure also includes a labile linker, which allows for the controlled release of the peptide from the solid support after synthesis. Its application is crucial in the production of complex peptides and proteins, enabling high purity and efficiency in biotechnological and pharmaceutical research. Additionally, it is employed in the development of peptide-based drugs and bioactive molecules due to its stability and compatibility with various synthetic protocols.
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