3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(9R)-10,11-dihydro-6'-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione
≥98%,99%d.e.
- Product Code: 70653
CAS:
1407166-63-5
| Molecular Weight: | 632.6 g./mol | Molecular Formula: | C₃₂H₃₀F₆N₄O₃ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily used in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex organic compounds, particularly those targeting specific biological pathways. Its structure is designed to interact with enzymes or receptors, making it valuable in the development of potential drug candidates. Researchers utilize it to explore its efficacy in inhibiting certain proteins or enzymes involved in disease processes, such as cancer or infectious diseases. Additionally, it may be employed in the study of chiral molecules due to its stereochemistry, aiding in the development of enantioselective drugs. Its unique trifluoromethyl groups enhance its stability and binding affinity, making it a promising candidate for further pharmacological investigations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,132.00 |
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3-[[3,5-Bis(trifluoromethyl)phenyl]amino]-4-[[(9R)-10,11-dihydro-6'-methoxycinchonan-9-yl]amino]-3-cyclobutene-1,2-dione
This chemical is primarily used in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of complex organic compounds, particularly those targeting specific biological pathways. Its structure is designed to interact with enzymes or receptors, making it valuable in the development of potential drug candidates. Researchers utilize it to explore its efficacy in inhibiting certain proteins or enzymes involved in disease processes, such as cancer or infectious diseases. Additionally, it may be employed in the study of chiral molecules due to its stereochemistry, aiding in the development of enantioselective drugs. Its unique trifluoromethyl groups enhance its stability and binding affinity, making it a promising candidate for further pharmacological investigations.
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