benzyl ((2S,3S)-1,1,1-trifluoro-2-hydroxy-4-methylpentan-3-yl)carbamate
95%
- Product Code: 64705
CAS:
291778-49-9
| Molecular Weight: | 305.29 g./mol | Molecular Formula: | C₁₄H₁₈F₃NO₃ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a trifluoro and hydroxy group, makes it a valuable intermediate in the synthesis of complex molecules, especially those targeting enzyme inhibition or receptor modulation. It is often employed in the preparation of peptidomimetics and other drug-like compounds due to its ability to introduce specific stereochemistry and functional groups. Additionally, its carbamate moiety can act as a protecting group for amines during multi-step synthetic processes, ensuring selective reactivity in complex reactions. This chemical is also explored in medicinal chemistry for the design of potential therapeutic agents, particularly in areas such as antiviral or anticancer research, where its unique properties can enhance drug efficacy and stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿26,748.00 |
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| 0.250 | 10-20 days | ฿50,148.00 |
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benzyl ((2S,3S)-1,1,1-trifluoro-2-hydroxy-4-methylpentan-3-yl)carbamate
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structure, featuring a trifluoro and hydroxy group, makes it a valuable intermediate in the synthesis of complex molecules, especially those targeting enzyme inhibition or receptor modulation. It is often employed in the preparation of peptidomimetics and other drug-like compounds due to its ability to introduce specific stereochemistry and functional groups. Additionally, its carbamate moiety can act as a protecting group for amines during multi-step synthetic processes, ensuring selective reactivity in complex reactions. This chemical is also explored in medicinal chemistry for the design of potential therapeutic agents, particularly in areas such as antiviral or anticancer research, where its unique properties can enhance drug efficacy and stability.
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