3-(((1R,2R)-2-(Piperidin-1-yl)cyclohexyl)amino)-4-((4-(trifluoromethyl)phenyl)amino)cyclobut-3-ene-1,2-dione
97%
- Product Code: 70622
CAS:
1211565-08-0
| Molecular Weight: | 421.50 g./mol | Molecular Formula: | C₂₂H₂₆F₃N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18411509 | |
| Melting Point: | 250 °C | Boiling Point: | 497.4±55.0 °C |
| Density: | 1.31±0.1 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of complex organic compounds. Its structure, featuring a cyclobutene-dione core and functional groups such as piperidine and trifluoromethylphenyl, makes it valuable for designing molecules with potential biological activity. It is often explored in the development of enzyme inhibitors, particularly those targeting proteins involved in signaling pathways or disease mechanisms. Researchers leverage its unique chemical framework to create analogs that can interact with specific biological targets, aiding in drug discovery efforts. Additionally, its trifluoromethyl group enhances metabolic stability and binding affinity, making it a useful component in the optimization of lead compounds for therapeutic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,616.00 |
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3-(((1R,2R)-2-(Piperidin-1-yl)cyclohexyl)amino)-4-((4-(trifluoromethyl)phenyl)amino)cyclobut-3-ene-1,2-dione
This chemical is primarily utilized in the field of medicinal chemistry, where it serves as a key intermediate in the synthesis of complex organic compounds. Its structure, featuring a cyclobutene-dione core and functional groups such as piperidine and trifluoromethylphenyl, makes it valuable for designing molecules with potential biological activity. It is often explored in the development of enzyme inhibitors, particularly those targeting proteins involved in signaling pathways or disease mechanisms. Researchers leverage its unique chemical framework to create analogs that can interact with specific biological targets, aiding in drug discovery efforts. Additionally, its trifluoromethyl group enhances metabolic stability and binding affinity, making it a useful component in the optimization of lead compounds for therapeutic applications.
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