Tert-Butyl 2-Oxa-3-Azabicyclo[2.2.2]Oct-5-Ene-3-Carboxylate
95%
- Product Code: 242837
CAS:
110590-29-9
| Molecular Weight: | 211.26 g./mol | Molecular Formula: | C₁₁H₁₇NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD24038975 | |
| Melting Point: | Boiling Point: | 280.1±20.0 °C(Predicted) | |
| Density: | 1.138±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its rigid bicyclic structure and built-in nitrogen functionality make it valuable for constructing complex molecules, especially in the development of enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for scaffold diversification and as a protecting group strategy in multi-step synthesis due to the stability of the tert-butyl carbamate (Boc) moiety. The compound’s alkene bridge allows for further functionalization via hydrogenation, epoxidation, or dihydroxylation, enabling versatile derivatization for drug discovery and combinatorial chemistry applications.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $579.47 |
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| 250mg | 10-20 days | $972.27 |
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| 1g | 10-20 days | $2,288.51 |
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Tert-Butyl 2-Oxa-3-Azabicyclo[2.2.2]Oct-5-Ene-3-Carboxylate
Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its rigid bicyclic structure and built-in nitrogen functionality make it valuable for constructing complex molecules, especially in the development of enzyme inhibitors and receptor ligands. Commonly employed in medicinal chemistry for scaffold diversification and as a protecting group strategy in multi-step synthesis due to the stability of the tert-butyl carbamate (Boc) moiety. The compound’s alkene bridge allows for further functionalization via hydrogenation, epoxidation, or dihydroxylation, enabling versatile derivatization for drug discovery and combinatorial chemistry applications.
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