(S)-Fmoc-2-amino-3-propargyloxy-propionic acid
98%
- Product Code: 236592
CAS:
1354752-75-2
| Molecular Weight: | 365.38 g./mol | Molecular Formula: | C₂₁H₁₉NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26793607 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Sealed |
Product Description:
Used in peptide synthesis as a chiral building block for incorporating propargyl-modified serine derivatives into peptides. The Fmoc group allows for solid-phase synthesis using standard Fmoc-strategy, while the propargyloxy side chain enables click chemistry modifications, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), for peptide conjugation, labeling, or immobilization. The (S)-configuration ensures stereochemical compatibility with natural amino acids, making it valuable in the design of bioactive peptides, peptidomimetics, and functional biomaterials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,340.00 |
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| 1.000 | 10-20 days | ฿3,430.00 |
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| 5.000 | 10-20 days | ฿13,160.00 |
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(S)-Fmoc-2-amino-3-propargyloxy-propionic acid
Used in peptide synthesis as a chiral building block for incorporating propargyl-modified serine derivatives into peptides. The Fmoc group allows for solid-phase synthesis using standard Fmoc-strategy, while the propargyloxy side chain enables click chemistry modifications, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), for peptide conjugation, labeling, or immobilization. The (S)-configuration ensures stereochemical compatibility with natural amino acids, making it valuable in the design of bioactive peptides, peptidomimetics, and functional biomaterials.
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