Racemic-(1R,4R)-5-Tert-Butyl 7-Methyl 2-Oxa-5-Azabicyclo[2.2.1]Heptane-5,7-Dicarboxylate
95%
- Product Code: 113025
CAS:
1823987-86-5
| Molecular Weight: | 257.28 g./mol | Molecular Formula: | C₁₂H₁₉NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27997337 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of complex molecules. Its bicyclic structure makes it a valuable building block for the synthesis of pharmaceuticals, particularly in the creation of chiral compounds that require precise stereochemistry. It is often employed in the preparation of active pharmaceutical ingredients (APIs) where the rigid framework of the bicyclic system helps in controlling the three-dimensional arrangement of atoms, which is crucial for biological activity. Additionally, its tert-butyl and methyl ester groups provide reactive sites for further functionalization, enabling chemists to tailor the molecule for specific applications in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £582.16 |
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| 0.250 | 10-20 days | £1,111.40 |
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Racemic-(1R,4R)-5-Tert-Butyl 7-Methyl 2-Oxa-5-Azabicyclo[2.2.1]Heptane-5,7-Dicarboxylate
This compound is primarily utilized in the field of organic synthesis as a key intermediate for the development of complex molecules. Its bicyclic structure makes it a valuable building block for the synthesis of pharmaceuticals, particularly in the creation of chiral compounds that require precise stereochemistry. It is often employed in the preparation of active pharmaceutical ingredients (APIs) where the rigid framework of the bicyclic system helps in controlling the three-dimensional arrangement of atoms, which is crucial for biological activity. Additionally, its tert-butyl and methyl ester groups provide reactive sites for further functionalization, enabling chemists to tailor the molecule for specific applications in drug discovery and development.
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