tert-butyl 4-(6-bromo-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate
95%
- Product Code: 87903
CAS:
1374145-59-1
| Molecular Weight: | 380.2797 g./mol | Molecular Formula: | C₁₇H₂₂BrN₃O₂ |
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| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring a bromo-substituted benzimidazole and a piperidine ring, makes it valuable for designing compounds with potential biological activity. It is often employed in the creation of drug candidates targeting various diseases, including cancer, infections, and neurological disorders. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the development of diverse chemical libraries for screening purposes. Additionally, its tert-butyloxycarbonyl (Boc) protecting group facilitates selective deprotection during multi-step synthetic processes, enhancing its utility in medicinal chemistry workflows.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,190.00 |
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| 0.250 | 10-20 days | ฿14,040.00 |
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| 1.000 | 10-20 days | ฿28,080.00 |
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tert-butyl 4-(6-bromo-1H-benzo[d]imidazol-1-yl)piperidine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of more complex molecules. Its structure, featuring a bromo-substituted benzimidazole and a piperidine ring, makes it valuable for designing compounds with potential biological activity. It is often employed in the creation of drug candidates targeting various diseases, including cancer, infections, and neurological disorders. The bromine atom allows for further functionalization through cross-coupling reactions, enabling the development of diverse chemical libraries for screening purposes. Additionally, its tert-butyloxycarbonyl (Boc) protecting group facilitates selective deprotection during multi-step synthetic processes, enhancing its utility in medicinal chemistry workflows.
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