Ethyl ((R)-(6-methoxyquinolin-4-yl)((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl) carbonate
97%
- Product Code: 82803
CAS:
83-75-0
| Molecular Weight: | 396.48 g./mol | Molecular Formula: | C₂₃H₂₈N₂O₄ |
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| EC Number: | MDL Number: | MFCD00198093 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry, particularly in the development of chiral drugs. Its structure, featuring a quinuclidine moiety and a methoxyquinoline group, makes it a valuable intermediate in the synthesis of enantiomerically pure pharmaceuticals. The compound is often employed in the production of antimalarial agents, leveraging the quinoline scaffold, which is known for its efficacy against Plasmodium species. Additionally, its chiral centers are exploited in asymmetric synthesis to create compounds with high stereochemical purity, which is crucial for the efficacy and safety of therapeutic agents. The vinyl group on the quinuclidine ring further allows for functionalization, enabling the creation of diverse derivatives for biological evaluation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $266.25 |
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| 0.250 | 10-20 days | $452.49 |
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| 1.000 | 10-20 days | $1,176.64 |
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Ethyl ((R)-(6-methoxyquinolin-4-yl)((1S,2S,4S,5R)-5-vinylquinuclidin-2-yl)methyl) carbonate
This compound is primarily utilized in the field of medicinal chemistry, particularly in the development of chiral drugs. Its structure, featuring a quinuclidine moiety and a methoxyquinoline group, makes it a valuable intermediate in the synthesis of enantiomerically pure pharmaceuticals. The compound is often employed in the production of antimalarial agents, leveraging the quinoline scaffold, which is known for its efficacy against Plasmodium species. Additionally, its chiral centers are exploited in asymmetric synthesis to create compounds with high stereochemical purity, which is crucial for the efficacy and safety of therapeutic agents. The vinyl group on the quinuclidine ring further allows for functionalization, enabling the creation of diverse derivatives for biological evaluation.
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