cis-tert-Butyl 3-hydroxy-4-methylpiperidine-1-carboxylate
≥95%
- Product Code: 84739
CAS:
955028-75-8
| Molecular Weight: | 215.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18791215 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It serves as a key building block in the pharmaceutical industry for the synthesis of various active pharmaceutical ingredients (APIs), particularly those targeting neurological and cardiovascular diseases. Its structure, featuring a piperidine ring and hydroxyl group, makes it a versatile precursor in the design of drugs that interact with biological receptors. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry plays a crucial role in achieving desired enantioselectivity in drug candidates. The tert-butyl group enhances stability, making it suitable for use in multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿13,500.00 |
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| 1.000 | 10-20 days | ฿28,800.00 |
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cis-tert-Butyl 3-hydroxy-4-methylpiperidine-1-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules. It serves as a key building block in the pharmaceutical industry for the synthesis of various active pharmaceutical ingredients (APIs), particularly those targeting neurological and cardiovascular diseases. Its structure, featuring a piperidine ring and hydroxyl group, makes it a versatile precursor in the design of drugs that interact with biological receptors. Additionally, it is employed in the preparation of chiral compounds, where its stereochemistry plays a crucial role in achieving desired enantioselectivity in drug candidates. The tert-butyl group enhances stability, making it suitable for use in multi-step synthetic processes.
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