1-(tert-Butoxycarbonyl)-2-methylpiperidine-2-carboxylic acid
97%
- Product Code: 114500
CAS:
746658-74-2
| Molecular Weight: | 243.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09910215 | |
| Melting Point: | Boiling Point: | 354.3°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This compound is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the development of active pharmaceutical ingredients (APIs) and other biologically active molecules. The tert-butoxycarbonyl (Boc) protecting group in its structure is crucial for safeguarding amine functionalities during multi-step synthetic processes, ensuring selective reactions. Its piperidine moiety is often incorporated into compounds targeting neurological and cardiovascular disorders, making it valuable for drug discovery and medicinal chemistry research. Additionally, its carboxylic acid group provides a versatile handle for further chemical modifications, enabling the creation of diverse derivatives for various applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,033.00 |
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| 5.000 | 10-20 days | ฿10,629.00 |
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| 10.000 | 10-20 days | ฿18,603.00 |
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1-(tert-Butoxycarbonyl)-2-methylpiperidine-2-carboxylic acid
This compound is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the development of active pharmaceutical ingredients (APIs) and other biologically active molecules. The tert-butoxycarbonyl (Boc) protecting group in its structure is crucial for safeguarding amine functionalities during multi-step synthetic processes, ensuring selective reactions. Its piperidine moiety is often incorporated into compounds targeting neurological and cardiovascular disorders, making it valuable for drug discovery and medicinal chemistry research. Additionally, its carboxylic acid group provides a versatile handle for further chemical modifications, enabling the creation of diverse derivatives for various applications.
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