(R)-1-(4-Chloro-2-(3-Methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethanol
98%
- Product Code: 54674
CAS:
1033805-26-3
| Molecular Weight: | 290.67 g./mol | Molecular Formula: | C₁₂H₁₀ClF₃N₂O |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 393.1±42.0℃(Predicted) | |
| Density: | 1.42±0.1 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzyme pathways or receptors. Its unique structure, featuring a trifluoroethanol group and a pyrazole ring, makes it valuable in designing compounds with enhanced binding affinity and metabolic stability. Researchers often employ it in the creation of potential therapeutic agents for conditions such as inflammation, cancer, or neurological disorders. Additionally, its chiral nature allows for the exploration of stereospecific interactions in drug design, contributing to the development of more effective and selective medications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £68.39 |
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| 0.250 | 10-20 days | £113.99 |
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| 1.000 | 10-20 days | £229.00 |
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(R)-1-(4-Chloro-2-(3-Methyl-1H-pyrazol-1-yl)phenyl)-2,2,2-trifluoroethanol
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting specific enzyme pathways or receptors. Its unique structure, featuring a trifluoroethanol group and a pyrazole ring, makes it valuable in designing compounds with enhanced binding affinity and metabolic stability. Researchers often employ it in the creation of potential therapeutic agents for conditions such as inflammation, cancer, or neurological disorders. Additionally, its chiral nature allows for the exploration of stereospecific interactions in drug design, contributing to the development of more effective and selective medications.
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