(1R,2S,4S)-rel-tert-Butyl 2-hydroxy-7-azabicyclo[2.2.1]heptane-7-carboxylate
97%
- Product Code: 228736
CAS:
154905-36-9
| Molecular Weight: | 213.2727 g./mol | Molecular Formula: | C₁₁H₁₉NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27966776 | |
| Melting Point: | Boiling Point: | 310.3±25.0 °C(Predicted) | |
| Density: | 1.181±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of neuroactive agents and enzyme inhibitors. Its rigid bicyclic structure and defined stereochemistry make it valuable for designing compounds that target central nervous system receptors, including those involved in pain management and neurological disorders. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to confer metabolic stability and enhance binding selectivity. Also utilized in asymmetric synthesis to introduce stereochemical control in complex molecule construction.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $619.92 |
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| 500mg | 10-20 days | $1,378.03 |
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(1R,2S,4S)-rel-tert-Butyl 2-hydroxy-7-azabicyclo[2.2.1]heptane-7-carboxylate
Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of neuroactive agents and enzyme inhibitors. Its rigid bicyclic structure and defined stereochemistry make it valuable for designing compounds that target central nervous system receptors, including those involved in pain management and neurological disorders. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to confer metabolic stability and enhance binding selectivity. Also utilized in asymmetric synthesis to introduce stereochemical control in complex molecule construction.
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