Fmoc-L-Tyr(propargyl)-OH
96%
- Product Code: 104326
CAS:
1204595-05-0
| Molecular Weight: | 441.48 g./mol | Molecular Formula: | C₂₇H₂₃NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26793610 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for introducing tyrosine residues with propargyl groups into peptide chains. The propargyl group allows for further functionalization through click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling the attachment of various tags, probes, or other molecules. This makes it valuable in the development of peptide-based drugs, bioconjugation studies, and the creation of peptide-antibody conjugates. Additionally, it is employed in the synthesis of peptides for research in biochemistry, molecular biology, and drug discovery, where site-specific modifications are required.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,022.00 |
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| 0.250 | 10-20 days | ฿8,532.00 |
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Fmoc-L-Tyr(propargyl)-OH
This compound is widely used in peptide synthesis, particularly in solid-phase peptide synthesis (SPPS) methods. It serves as a building block for introducing tyrosine residues with propargyl groups into peptide chains. The propargyl group allows for further functionalization through click chemistry, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling the attachment of various tags, probes, or other molecules. This makes it valuable in the development of peptide-based drugs, bioconjugation studies, and the creation of peptide-antibody conjugates. Additionally, it is employed in the synthesis of peptides for research in biochemistry, molecular biology, and drug discovery, where site-specific modifications are required.
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