Racemic-(3aS,8R,8aS)-tert-butyl 8-hydroxy-3,3a,8,8a-tetrahydroindeno[1,2-c]pyrrole-2(1H)-carboxylate
95%
- Product Code: 87083
CAS:
1350475-48-7
| Molecular Weight: | 275.35 g./mol | Molecular Formula: | C₁₆H₂₁NO₃ |
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| EC Number: | MDL Number: | MFCD26131423 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. Its unique structure, featuring a tetrahydroindeno-pyrrole core, makes it valuable in the synthesis of biologically active compounds, particularly in pharmaceutical research. It is often employed in the construction of heterocyclic frameworks that are essential for drug discovery, especially in the development of potential therapeutic agents targeting neurological disorders or other diseases. The tert-butyl and carboxylate groups in its structure provide versatility in further chemical modifications, enabling the creation of diverse derivatives for screening and optimization in medicinal chemistry. Additionally, its chiral centers offer opportunities for enantioselective synthesis, which is crucial for producing compounds with specific biological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £453.72 |
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Racemic-(3aS,8R,8aS)-tert-butyl 8-hydroxy-3,3a,8,8a-tetrahydroindeno[1,2-c]pyrrole-2(1H)-carboxylate
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of more complex molecules. Its unique structure, featuring a tetrahydroindeno-pyrrole core, makes it valuable in the synthesis of biologically active compounds, particularly in pharmaceutical research. It is often employed in the construction of heterocyclic frameworks that are essential for drug discovery, especially in the development of potential therapeutic agents targeting neurological disorders or other diseases. The tert-butyl and carboxylate groups in its structure provide versatility in further chemical modifications, enabling the creation of diverse derivatives for screening and optimization in medicinal chemistry. Additionally, its chiral centers offer opportunities for enantioselective synthesis, which is crucial for producing compounds with specific biological activities.
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