tert-Butyl 3-hydroxy-3-phenylpiperidine-1-carboxylate
95%
- Product Code: 45621
CAS:
213923-81-0
| Molecular Weight: | 277.3587 g./mol | Molecular Formula: | C₁₆H₂₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09953390 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of various pharmaceutical agents. Its structure, featuring both a piperidine ring and a phenyl group, makes it a valuable building block in the development of bioactive molecules. It is often employed in the synthesis of compounds targeting neurological disorders, such as inhibitors for enzymes or receptors involved in the central nervous system. Additionally, it serves as a precursor in the creation of ligands for drug discovery, particularly in the design of molecules with potential analgesic or anti-inflammatory properties. Its tert-butyloxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile tool in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,480.00 |
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tert-Butyl 3-hydroxy-3-phenylpiperidine-1-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of various pharmaceutical agents. Its structure, featuring both a piperidine ring and a phenyl group, makes it a valuable building block in the development of bioactive molecules. It is often employed in the synthesis of compounds targeting neurological disorders, such as inhibitors for enzymes or receptors involved in the central nervous system. Additionally, it serves as a precursor in the creation of ligands for drug discovery, particularly in the design of molecules with potential analgesic or anti-inflammatory properties. Its tert-butyloxycarbonyl (Boc) protecting group allows for selective reactions, making it a versatile tool in multi-step synthetic processes.
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