1-Cyclobutyl-6-difluoromethoxy-1H-indole-3-carbonitrile
≥95%
- Product Code: 80552
CAS:
1248585-30-9
| Molecular Weight: | 262.25 g./mol | Molecular Formula: | C₁₄H₁₂F₂N₂O |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structural features, including the cyclobutyl group and difluoromethoxy moiety, make it a valuable building block for developing potential drug candidates, particularly in the area of kinase inhibitors. These inhibitors are often explored for treating various diseases, including cancer and inflammatory disorders. Additionally, the indole core structure of this compound is frequently employed in the design of compounds targeting neurological conditions, such as depression or anxiety, due to its ability to interact with serotonin receptors. Its carbonitrile group further enhances its utility by providing a reactive site for further chemical modifications, enabling the creation of diverse derivatives for pharmacological screening.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | ฿5,580.00 |
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| 0.050 | 10-20 days | ฿16,560.00 |
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1-Cyclobutyl-6-difluoromethoxy-1H-indole-3-carbonitrile
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structural features, including the cyclobutyl group and difluoromethoxy moiety, make it a valuable building block for developing potential drug candidates, particularly in the area of kinase inhibitors. These inhibitors are often explored for treating various diseases, including cancer and inflammatory disorders. Additionally, the indole core structure of this compound is frequently employed in the design of compounds targeting neurological conditions, such as depression or anxiety, due to its ability to interact with serotonin receptors. Its carbonitrile group further enhances its utility by providing a reactive site for further chemical modifications, enabling the creation of diverse derivatives for pharmacological screening.
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