(2R,4R)-tert-Butyl 4-hydroxy-2-methylpiperidine-1-carboxylate
98%
- Product Code: 70860
CAS:
790667-44-6
| Molecular Weight: | 215.29 g./mol | Molecular Formula: | C₁₁H₂₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23105950 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a chiral building block or intermediate. Its stereochemistry makes it valuable in the production of enantiomerically pure pharmaceuticals, particularly in the synthesis of complex molecules where specific spatial orientation is crucial for biological activity. It is often employed in the development of drugs targeting the central nervous system, as its structural features can enhance binding affinity to specific receptors. Additionally, its tert-butyl and carboxylate groups provide stability and reactivity, making it suitable for use in peptide coupling reactions or as a protecting group in multi-step synthetic processes. Its application extends to agrochemical research, where it serves as a precursor in the design of active ingredients with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,663.00 |
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| 1.000 | 10-20 days | ฿8,910.00 |
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| 5.000 | 10-20 days | ฿27,027.00 |
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(2R,4R)-tert-Butyl 4-hydroxy-2-methylpiperidine-1-carboxylate
This compound is primarily utilized in the field of organic synthesis as a chiral building block or intermediate. Its stereochemistry makes it valuable in the production of enantiomerically pure pharmaceuticals, particularly in the synthesis of complex molecules where specific spatial orientation is crucial for biological activity. It is often employed in the development of drugs targeting the central nervous system, as its structural features can enhance binding affinity to specific receptors. Additionally, its tert-butyl and carboxylate groups provide stability and reactivity, making it suitable for use in peptide coupling reactions or as a protecting group in multi-step synthetic processes. Its application extends to agrochemical research, where it serves as a precursor in the design of active ingredients with improved efficacy and selectivity.
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