Rel-(1S,2R,4S,5R)-tert-butyl 7-oxo-3-oxa-6-azatricyclo[3.2.1.02,4]octane-6-carboxylate
95%
- Product Code: 57688
CAS:
244057-70-3
| Molecular Weight: | 225.24 g./mol | Molecular Formula: | C₁₁H₁₅NO₄ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 120-122 °C | Boiling Point: | 377.5±35.0 °C(Predicted) |
| Density: | 1.326±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate in the production of complex molecules. Its unique tricyclic structure makes it valuable for constructing frameworks often found in pharmaceuticals, particularly in the development of drugs targeting neurological and cardiovascular disorders. It is also employed in the synthesis of chiral compounds, where its stereochemistry plays a crucial role in achieving high enantioselectivity. Additionally, its tert-butyl ester group provides stability and ease of manipulation in various chemical reactions, making it a versatile building block in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $598.15 |
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| 0.250 | 10-20 days | $1,058.26 |
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Rel-(1S,2R,4S,5R)-tert-butyl 7-oxo-3-oxa-6-azatricyclo[3.2.1.02,4]octane-6-carboxylate
This compound is primarily utilized in the field of organic synthesis as a key intermediate in the production of complex molecules. Its unique tricyclic structure makes it valuable for constructing frameworks often found in pharmaceuticals, particularly in the development of drugs targeting neurological and cardiovascular disorders. It is also employed in the synthesis of chiral compounds, where its stereochemistry plays a crucial role in achieving high enantioselectivity. Additionally, its tert-butyl ester group provides stability and ease of manipulation in various chemical reactions, making it a versatile building block in medicinal chemistry and drug discovery processes.
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