tert-Butyl 4-(piperazin-1-yl)piperidine-1-carboxylate
98%
- Product Code: 152882
CAS:
177276-41-4
| Molecular Weight: | 269.38 g./mol | Molecular Formula: | C₁₄H₂₇N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04973999 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, drying away from light |
Product Description:
Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in the development of bioactive molecules, particularly in the creation of receptor agonists and antagonists. Its structure allows for easy modification of both piperazine and piperidine moieties, making it valuable in medicinal chemistry for optimizing drug candidates targeting central nervous system disorders, including anxiety, depression, and schizophrenia. It is also employed in the design of kinase inhibitors and other enzyme modulators due to its favorable solubility and binding properties. The tert-butyl carbamate (Boc) group provides protection during peptide coupling and multi-step syntheses, enabling selective reactions in complex molecule assembly.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,680.00 |
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| 1.000 | 10-20 days | ฿7,440.00 |
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| 5.000 | 10-20 days | ฿25,940.00 |
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| 10.000 | 10-20 days | ฿50,440.00 |
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tert-Butyl 4-(piperazin-1-yl)piperidine-1-carboxylate
Widely used in pharmaceutical synthesis, this compound serves as a key intermediate in the development of bioactive molecules, particularly in the creation of receptor agonists and antagonists. Its structure allows for easy modification of both piperazine and piperidine moieties, making it valuable in medicinal chemistry for optimizing drug candidates targeting central nervous system disorders, including anxiety, depression, and schizophrenia. It is also employed in the design of kinase inhibitors and other enzyme modulators due to its favorable solubility and binding properties. The tert-butyl carbamate (Boc) group provides protection during peptide coupling and multi-step syntheses, enabling selective reactions in complex molecule assembly.
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