TERT-BUTYL 6'-CHLORO-1',2'-DIHYDROSPIRO[PIPERIDINE-4,3'-PYRROLO[3,2-B]PYRIDINE]-1-CARBOXYLATE
95%
- Product Code: 75932
CAS:
857730-15-5
| Molecular Weight: | 324 g./mol | Molecular Formula: | C₁₆H₂₂ClN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27992044 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a spirocyclic framework and a piperidine ring, makes it a valuable building block for designing drugs targeting central nervous system disorders, such as anxiety, depression, or neurodegenerative diseases. Additionally, its chloro and ester functional groups provide reactive sites for further chemical modifications, enabling the creation of diverse derivatives for medicinal chemistry studies. Its application is also explored in the development of kinase inhibitors, which are crucial in cancer therapy. Researchers leverage its unique scaffold to optimize drug potency, selectivity, and pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿87,360.00 |
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| 1.000 | 10-20 days | ฿229,900.00 |
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TERT-BUTYL 6'-CHLORO-1',2'-DIHYDROSPIRO[PIPERIDINE-4,3'-PYRROLO[3,2-B]PYRIDINE]-1-CARBOXYLATE
This compound is primarily utilized in pharmaceutical research and development, particularly as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a spirocyclic framework and a piperidine ring, makes it a valuable building block for designing drugs targeting central nervous system disorders, such as anxiety, depression, or neurodegenerative diseases. Additionally, its chloro and ester functional groups provide reactive sites for further chemical modifications, enabling the creation of diverse derivatives for medicinal chemistry studies. Its application is also explored in the development of kinase inhibitors, which are crucial in cancer therapy. Researchers leverage its unique scaffold to optimize drug potency, selectivity, and pharmacokinetic properties.
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