N-Fmoc-3-(2-propyn-1-yloxy)-L-phenylalanine
98%
- Product Code: 220592
CAS:
1454817-57-2
| Molecular Weight: | 441.48 g./mol | Molecular Formula: | C₂₇H₂₃NO₅ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Used in solid-phase peptide synthesis, this compound enables the incorporation of alkyne-functionalized amino acids into peptides. The alkyne group allows for bioorthogonal reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), commonly known as click chemistry. This is particularly valuable in labeling peptides with fluorescent tags, biotin, or other functional probes for imaging, detection, or pull-down assays. The Fmoc protection group ensures compatibility with standard Fmoc-t-Bu strategy, allowing stepwise assembly of complex peptides on resin. Its main application lies in the development of peptide-based probes, conjugation strategies, and chemical biology research where site-specific modification is required.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿5,500.00 |
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N-Fmoc-3-(2-propyn-1-yloxy)-L-phenylalanine
Used in solid-phase peptide synthesis, this compound enables the incorporation of alkyne-functionalized amino acids into peptides. The alkyne group allows for bioorthogonal reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), commonly known as click chemistry. This is particularly valuable in labeling peptides with fluorescent tags, biotin, or other functional probes for imaging, detection, or pull-down assays. The Fmoc protection group ensures compatibility with standard Fmoc-t-Bu strategy, allowing stepwise assembly of complex peptides on resin. Its main application lies in the development of peptide-based probes, conjugation strategies, and chemical biology research where site-specific modification is required.
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