tert-Butyl ((S)-4-methyl-1-((R)-2-methyloxiran-2-yl)-1-oxopentan-2-yl)carbamate
≥95%
- Product Code: 121438
CAS:
247068-82-2
| Molecular Weight: | 271.35 g./mol | Molecular Formula: | C₁₄H₂₅NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22573306 | |
| Melting Point: | Boiling Point: | 369.8±37.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of protease inhibitors, which are crucial for treating diseases such as HIV and hepatitis C. Its structure, featuring both a tert-butyl carbamate group and an epoxide, makes it valuable for constructing chiral centers and enabling stereoselective reactions. Additionally, it is employed in the development of peptide-based drugs, where its protective groups and reactive sites facilitate controlled modifications and efficient coupling reactions. Its application extends to medicinal chemistry for designing and optimizing bioactive compounds with enhanced therapeutic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,854.00 |
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| 1.000 | 10-20 days | ฿5,139.00 |
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| 5.000 | 10-20 days | ฿25,659.00 |
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tert-Butyl ((S)-4-methyl-1-((R)-2-methyloxiran-2-yl)-1-oxopentan-2-yl)carbamate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the production of protease inhibitors, which are crucial for treating diseases such as HIV and hepatitis C. Its structure, featuring both a tert-butyl carbamate group and an epoxide, makes it valuable for constructing chiral centers and enabling stereoselective reactions. Additionally, it is employed in the development of peptide-based drugs, where its protective groups and reactive sites facilitate controlled modifications and efficient coupling reactions. Its application extends to medicinal chemistry for designing and optimizing bioactive compounds with enhanced therapeutic properties.
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