tert-butyl (R)-4-(1-hydroxyethyl)piperidine-1-carboxylate
95%
- Product Code: 229134
Alias:
4-[(1R)-1-hydroxyethyl]piperidine-1-carboxylic acid tert-butyl ester; (R)-1-(1-BOC-4-piperidine)ethanol
CAS:
1206830-71-8
| Molecular Weight: | 229.31 g./mol | Molecular Formula: | C₁₂H₂₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22666104 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Sealed |
Product Description:
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected piperidine structure with a hydroxyethyl group makes it valuable in constructing complex molecules for central nervous system agents, including antidepressants and antipsychotics. The tert-butyl carbamate (Boc) group allows for selective protection during peptide coupling or heterocycle formation, enabling stepwise assembly in multi-step organic syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical stability and functional group compatibility.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿4,150.00 |
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| 250mg | 10-20 days | ฿7,320.00 |
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| 1g | 10-20 days | ฿19,980.00 |
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tert-butyl (R)-4-(1-hydroxyethyl)piperidine-1-carboxylate
Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected piperidine structure with a hydroxyethyl group makes it valuable in constructing complex molecules for central nervous system agents, including antidepressants and antipsychotics. The tert-butyl carbamate (Boc) group allows for selective protection during peptide coupling or heterocycle formation, enabling stepwise assembly in multi-step organic syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical stability and functional group compatibility.
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