6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-norleucine
98%
- Product Code: 65209
CAS:
159610-89-6
| Molecular Weight: | 394.43 g./mol | Molecular Formula: | C₂₁H₂₂N₄O₄ |
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| EC Number: | MDL Number: | MFCD13182319 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in peptide synthesis and bioconjugation processes. It serves as a building block for introducing azide functionalities into peptides, which are essential for click chemistry reactions. The azide group enables efficient and selective coupling with alkyne-containing molecules, facilitating the creation of complex biomolecular structures. Additionally, the fluorenylmethoxycarbonyl (Fmoc) protecting group ensures controlled deprotection during solid-phase peptide synthesis, enhancing precision in peptide chain assembly. Its application is particularly valuable in drug development, protein engineering, and the study of biomolecular interactions, where site-specific modifications are crucial.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | Ft10,860.30 |
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| 0.250 | 10-20 days | Ft30,835.50 |
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6-Azido-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-L-norleucine
This compound is primarily utilized in peptide synthesis and bioconjugation processes. It serves as a building block for introducing azide functionalities into peptides, which are essential for click chemistry reactions. The azide group enables efficient and selective coupling with alkyne-containing molecules, facilitating the creation of complex biomolecular structures. Additionally, the fluorenylmethoxycarbonyl (Fmoc) protecting group ensures controlled deprotection during solid-phase peptide synthesis, enhancing precision in peptide chain assembly. Its application is particularly valuable in drug development, protein engineering, and the study of biomolecular interactions, where site-specific modifications are crucial.
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