Boc-Thr(Fmoc-Val)-OH
≥95%
- Product Code: 36532
CAS:
887707-95-1
| Molecular Weight: | 540.60 g./mol | Molecular Formula: | C₂₉H₃₆N₂O₈ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11974993 | |
| Melting Point: | Boiling Point: | 728.8±60.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptide chains, particularly in solid-phase peptide synthesis (SPPS). The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Fmoc (9-fluorenylmethyloxycarbonyl) group safeguards the valine side chain. This dual protection allows for selective deprotection and coupling reactions, enabling the stepwise assembly of peptides with high precision. It is especially valuable in synthesizing peptides with specific sequences for research in biochemistry, pharmaceuticals, and drug development. Its application ensures efficient and controlled peptide elongation, minimizing side reactions and improving yield.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,097.00 |
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Boc-Thr(Fmoc-Val)-OH
This compound is primarily utilized in peptide synthesis as a protected amino acid derivative. It serves as a building block for constructing complex peptide chains, particularly in solid-phase peptide synthesis (SPPS). The Boc (tert-butyloxycarbonyl) group protects the amino group, while the Fmoc (9-fluorenylmethyloxycarbonyl) group safeguards the valine side chain. This dual protection allows for selective deprotection and coupling reactions, enabling the stepwise assembly of peptides with high precision. It is especially valuable in synthesizing peptides with specific sequences for research in biochemistry, pharmaceuticals, and drug development. Its application ensures efficient and controlled peptide elongation, minimizing side reactions and improving yield.
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