rel-(2R,4R)-tert-Butyl 4-amino-2-(hydroxymethyl)piperidine-1-carboxylate
97%
- Product Code: 50601
CAS:
1402249-04-0
| Molecular Weight: | 230.3040 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD20922052 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both amino and hydroxymethyl functional groups, makes it a valuable building block in organic synthesis. It is often employed in the preparation of complex molecules, such as protease inhibitors and other therapeutic agents targeting various diseases. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, which is critical in drug development to ensure efficacy and reduce side effects. The tert-butyl group provides steric protection, enhancing the stability of the intermediate during chemical reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $1,215.97 |
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rel-(2R,4R)-tert-Butyl 4-amino-2-(hydroxymethyl)piperidine-1-carboxylate
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring both amino and hydroxymethyl functional groups, makes it a valuable building block in organic synthesis. It is often employed in the preparation of complex molecules, such as protease inhibitors and other therapeutic agents targeting various diseases. Additionally, its chiral nature allows for the creation of enantiomerically pure compounds, which is critical in drug development to ensure efficacy and reduce side effects. The tert-butyl group provides steric protection, enhancing the stability of the intermediate during chemical reactions.
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