8-Fluoroquinoline-4-carbaldehyde
95%
- Product Code: 54354
CAS:
496792-30-4
| Molecular Weight: | 175.1592 g./mol | Molecular Formula: | C₁₀H₆FNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06824407 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both a fluorine atom and an aldehyde group, makes it particularly useful in the creation of heterocyclic compounds, which are often explored for their potential pharmaceutical applications. Researchers frequently employ it in the synthesis of quinoline derivatives, which are known for their biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, the aldehyde group allows for further functionalization through reactions such as condensation, making it a valuable intermediate in medicinal chemistry and drug discovery. Its incorporation into larger molecular frameworks can enhance the binding affinity and selectivity of potential drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿6,138.00 |
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8-Fluoroquinoline-4-carbaldehyde
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring both a fluorine atom and an aldehyde group, makes it particularly useful in the creation of heterocyclic compounds, which are often explored for their potential pharmaceutical applications. Researchers frequently employ it in the synthesis of quinoline derivatives, which are known for their biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, the aldehyde group allows for further functionalization through reactions such as condensation, making it a valuable intermediate in medicinal chemistry and drug discovery. Its incorporation into larger molecular frameworks can enhance the binding affinity and selectivity of potential drug candidates.
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