tert-butyl 4-((2-bromophenyl)amino)-4-cyanopiperidine-1-carboxylate
95%
- Product Code: 83756
CAS:
205813-91-8
| Molecular Weight: | 380.28 g./mol | Molecular Formula: | C₁₇H₂₂BrN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31706248 | |
| Melting Point: | Boiling Point: | 503.0±50.0 °C(Predicted) | |
| Density: | 1.37±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, including potential drug candidates. Its structure, featuring a piperidine ring, a cyano group, and a bromophenyl moiety, makes it valuable for constructing complex molecules with specific pharmacological properties. Researchers often employ it in the design and optimization of compounds targeting neurological disorders, cancer, or infectious diseases. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and development.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | €246.19 |
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| 250mg | 10-20 days | €461.60 |
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| 1g | 10-20 days | €923.20 |
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tert-butyl 4-((2-bromophenyl)amino)-4-cyanopiperidine-1-carboxylate
This chemical is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a key intermediate in the synthesis of various biologically active molecules, including potential drug candidates. Its structure, featuring a piperidine ring, a cyano group, and a bromophenyl moiety, makes it valuable for constructing complex molecules with specific pharmacological properties. Researchers often employ it in the design and optimization of compounds targeting neurological disorders, cancer, or infectious diseases. Additionally, its reactive sites allow for further functionalization, enabling the creation of diverse chemical libraries for drug discovery and development.
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