tert-Butyl 4-(2-methyl-5-(trifluoromethyl)-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate
97%
- Product Code: 46161
CAS:
1262400-72-5
| Molecular Weight: | 383.41 g./mol | Molecular Formula: | C₁₉H₂₄F₃N₃O₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical and medicinal chemistry fields as an intermediate in the synthesis of biologically active molecules. It is particularly significant in the development of potential drug candidates targeting various therapeutic areas, such as central nervous system disorders, cancer, and infectious diseases. Its structure, featuring a benzimidazole core and a piperidine moiety, makes it a versatile building block for designing compounds with specific receptor-binding properties. Researchers often employ it in the optimization of drug-like properties, including bioavailability, metabolic stability, and selectivity. Additionally, its trifluoromethyl group enhances the compound's lipophilicity and binding affinity, making it valuable in the creation of potent and selective inhibitors or modulators for specific biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,174.00 |
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tert-Butyl 4-(2-methyl-5-(trifluoromethyl)-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical and medicinal chemistry fields as an intermediate in the synthesis of biologically active molecules. It is particularly significant in the development of potential drug candidates targeting various therapeutic areas, such as central nervous system disorders, cancer, and infectious diseases. Its structure, featuring a benzimidazole core and a piperidine moiety, makes it a versatile building block for designing compounds with specific receptor-binding properties. Researchers often employ it in the optimization of drug-like properties, including bioavailability, metabolic stability, and selectivity. Additionally, its trifluoromethyl group enhances the compound's lipophilicity and binding affinity, making it valuable in the creation of potent and selective inhibitors or modulators for specific biological targets.
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