tert-Butyl ((2S,3R)-3-hydroxy-4-(isobutylamino)-1-phenylbutan-2-yl)carbamate
≥96%
- Product Code: 36524
CAS:
160232-08-6
| Molecular Weight: | 336.47 g./mol | Molecular Formula: | C₁₉H₃₂N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15144668 | |
| Melting Point: | Boiling Point: | 484.7°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of complex molecules, particularly in the development of protease inhibitors. These inhibitors are crucial in treating diseases such as HIV and hepatitis C, as they block viral replication. The compound’s chiral structure allows it to act as a building block for creating enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it is utilized in peptide chemistry for protecting amine groups during multi-step organic synthesis, enabling the precise construction of biologically active peptides. Its stability and reactivity make it valuable in research and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $40.77 |
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| 0.250 | 10-20 days | $65.35 |
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| 1.000 | 10-20 days | $102.88 |
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tert-Butyl ((2S,3R)-3-hydroxy-4-(isobutylamino)-1-phenylbutan-2-yl)carbamate
This compound is primarily used in the pharmaceutical industry as an intermediate in the synthesis of complex molecules, particularly in the development of protease inhibitors. These inhibitors are crucial in treating diseases such as HIV and hepatitis C, as they block viral replication. The compound’s chiral structure allows it to act as a building block for creating enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it is utilized in peptide chemistry for protecting amine groups during multi-step organic synthesis, enabling the precise construction of biologically active peptides. Its stability and reactivity make it valuable in research and drug discovery processes.
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