3-Fluoro-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde
98%
- Product Code: 44806
CAS:
937400-07-2
| Molecular Weight: | 204.2 g./mol | Molecular Formula: | C₁₁H₉FN₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13180648 | |
| Melting Point: | Boiling Point: | ||
| 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 various biologically active molecules. Its structure, featuring both a fluorine atom and an imidazole ring, makes it a valuable building block for developing pharmaceuticals, particularly in the design of enzyme inhibitors and receptor antagonists. The presence of the aldehyde group allows for further functionalization, enabling the creation of diverse chemical entities. It is often employed in research targeting the development of drugs for conditions such as inflammation, cancer, and neurological disorders. Additionally, its unique structure contributes to the optimization of drug candidates by enhancing binding affinity and selectivity toward specific biological targets.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $193.60 |
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3-Fluoro-4-(4-methyl-1H-imidazol-1-yl)benzaldehyde
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a fluorine atom and an imidazole ring, makes it a valuable building block for developing pharmaceuticals, particularly in the design of enzyme inhibitors and receptor antagonists. The presence of the aldehyde group allows for further functionalization, enabling the creation of diverse chemical entities. It is often employed in research targeting the development of drugs for conditions such as inflammation, cancer, and neurological disorders. Additionally, its unique structure contributes to the optimization of drug candidates by enhancing binding affinity and selectivity toward specific biological targets.
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