(S)-Methyl 3-((tert-butoxycarbonyl)amino)-3-methyl-2-(((S)-1-phenylethyl)amino)butanoate
≥95%
- Product Code: 38379
CAS:
1093192-06-3
| Molecular Weight: | 350.45 g./mol | Molecular Formula: | C₁₉H₃₀N₂O₄ |
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| EC Number: | MDL Number: | MFCD27992079 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of chiral drugs, where its stereochemical properties are crucial for achieving the desired biological activity. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during multi-step syntheses, while the chiral centers allow for the creation of enantiomerically pure compounds. It is often employed in peptide chemistry and the development of enzyme inhibitors, leveraging its structural features to enhance drug efficacy and specificity. Additionally, it finds application in research focused on asymmetric synthesis, aiding in the study of stereoselective reactions and the development of novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €65.77 |
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| 0.250 | 10-20 days | €109.93 |
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| 1.000 | 10-20 days | €329.80 |
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(S)-Methyl 3-((tert-butoxycarbonyl)amino)-3-methyl-2-(((S)-1-phenylethyl)amino)butanoate
This compound is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of chiral drugs, where its stereochemical properties are crucial for achieving the desired biological activity. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during multi-step syntheses, while the chiral centers allow for the creation of enantiomerically pure compounds. It is often employed in peptide chemistry and the development of enzyme inhibitors, leveraging its structural features to enhance drug efficacy and specificity. Additionally, it finds application in research focused on asymmetric synthesis, aiding in the study of stereoselective reactions and the development of novel therapeutic agents.
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