(3aR,7aS)-rel-tert-Butyl 5-hydroxyhexahydro-1H-isoindole-2(3H)-carboxylate
96%
- Product Code: 123635
CAS:
318502-89-5
| Molecular Weight: | 241.33 g./mol | Molecular Formula: | C₁₃H₂₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23106330 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of complex organic molecules. Its structure, featuring a hexahydro-isoindole core, makes it valuable for constructing biologically active compounds, particularly in the field of drug discovery. It is often employed in the preparation of potential therapeutic agents targeting neurological disorders, owing to its ability to interact with specific biological pathways. Additionally, its tert-butyl ester group provides stability and facilitates further chemical modifications, making it a versatile building block in medicinal chemistry. Researchers also explore its use in creating peptidomimetics, which mimic peptide structures for enhanced drug efficacy and stability.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,543.00 |
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| 0.250 | 10-20 days | ฿10,899.00 |
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(3aR,7aS)-rel-tert-Butyl 5-hydroxyhexahydro-1H-isoindole-2(3H)-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of complex organic molecules. Its structure, featuring a hexahydro-isoindole core, makes it valuable for constructing biologically active compounds, particularly in the field of drug discovery. It is often employed in the preparation of potential therapeutic agents targeting neurological disorders, owing to its ability to interact with specific biological pathways. Additionally, its tert-butyl ester group provides stability and facilitates further chemical modifications, making it a versatile building block in medicinal chemistry. Researchers also explore its use in creating peptidomimetics, which mimic peptide structures for enhanced drug efficacy and stability.
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