Fmoc-Phe(4-N3)-OH
95%
- Product Code: 66183
CAS:
163217-43-4
| Molecular Weight: | 428.44 g./mol | Molecular Formula: | C₂₄H₂₀N₄O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00237665 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C |
Product Description:
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for introducing azide-functionalized phenylalanine residues into peptide chains. The azide group allows for subsequent click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling the attachment of various functional groups or labels to the peptide. This makes it valuable in bioconjugation, drug discovery, and the development of peptide-based probes for biological studies. Additionally, its Fmoc protecting group ensures compatibility with standard SPPS protocols, facilitating efficient and controlled peptide assembly.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,920.00 |
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Fmoc-Phe(4-N3)-OH
This chemical is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for introducing azide-functionalized phenylalanine residues into peptide chains. The azide group allows for subsequent click chemistry reactions, such as the copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling the attachment of various functional groups or labels to the peptide. This makes it valuable in bioconjugation, drug discovery, and the development of peptide-based probes for biological studies. Additionally, its Fmoc protecting group ensures compatibility with standard SPPS protocols, facilitating efficient and controlled peptide assembly.
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