1-(tert-Butyl) 3-methyl (R)-piperidine-1,3-dicarboxylate
98%
- Product Code: 66393
CAS:
934423-10-6
| Molecular Weight: | 243.3 g./mol | Molecular Formula: | C₁₂H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD09955429 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of various bioactive compounds. Its structure, featuring a piperidine ring and carboxylate groups, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting the central nervous system. It is often employed in asymmetric synthesis due to its chiral center, enabling the creation of enantiomerically pure substances. Additionally, it serves as a building block in the synthesis of alkaloids and other nitrogen-containing heterocycles, which are crucial in medicinal chemistry. Its tert-butyl and methyl ester groups provide versatility in protecting and deprotecting strategies during multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,439.00 |
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| 0.250 | 10-20 days | ฿3,654.00 |
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| 1.000 | 10-20 days | ฿9,126.00 |
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1-(tert-Butyl) 3-methyl (R)-piperidine-1,3-dicarboxylate
This chemical is primarily utilized in the pharmaceutical and organic synthesis industries as a key intermediate in the production of various bioactive compounds. Its structure, featuring a piperidine ring and carboxylate groups, makes it valuable for constructing complex molecules, particularly in the development of drugs targeting the central nervous system. It is often employed in asymmetric synthesis due to its chiral center, enabling the creation of enantiomerically pure substances. Additionally, it serves as a building block in the synthesis of alkaloids and other nitrogen-containing heterocycles, which are crucial in medicinal chemistry. Its tert-butyl and methyl ester groups provide versatility in protecting and deprotecting strategies during multi-step synthetic processes.
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