(2S,4S)-tert-butyl 5-amino-2-((tert-butoxycarbonyl)(2,4,6-trimethoxybenzyl)amino)-5-oxo-4-(tosyloxy)pentanoate
95%
- Product Code: 236368
CAS:
1262523-66-9
| Molecular Weight: | 652.75 g./mol | Molecular Formula: | C₃₁H₄₄N₂O₁₁S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 801.0±65.0 °C(Predicted) | |
| Density: | 1.208±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature |
Product Description:
Used as a key intermediate in the synthesis of complex peptide-based pharmaceuticals, particularly in the preparation of protease inhibitors. Its protected amine and hydroxyl groups allow for selective coupling reactions, making it valuable in solid-phase peptide synthesis. The presence of the tosyloxy group enables displacement reactions for carbon-carbon bond formation, while the bulky protecting groups enhance stereochemical control during multi-step syntheses. Commonly employed in the development of antiviral and anticancer agents where precise chirality and functional group compatibility are critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.001 | 10-20 days | ฿37,010.00 |
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(2S,4S)-tert-butyl 5-amino-2-((tert-butoxycarbonyl)(2,4,6-trimethoxybenzyl)amino)-5-oxo-4-(tosyloxy)pentanoate
Used as a key intermediate in the synthesis of complex peptide-based pharmaceuticals, particularly in the preparation of protease inhibitors. Its protected amine and hydroxyl groups allow for selective coupling reactions, making it valuable in solid-phase peptide synthesis. The presence of the tosyloxy group enables displacement reactions for carbon-carbon bond formation, while the bulky protecting groups enhance stereochemical control during multi-step syntheses. Commonly employed in the development of antiviral and anticancer agents where precise chirality and functional group compatibility are critical.
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