Ethyl 3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate
95%
- Product Code: 84048
CAS:
866588-11-6
| Molecular Weight: | 234.23 g./mol | Molecular Formula: | C₁₂H₁₁FN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08445938 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a pyrazole ring and a fluorophenyl group, makes it a valuable building block for developing compounds with potential therapeutic applications. Researchers often utilize it to create derivatives that are tested for anti-inflammatory, analgesic, and antimicrobial properties. Additionally, it plays a role in the development of pharmaceuticals targeting central nervous system disorders, owing to its ability to interact with specific biological receptors. Its fluorinated aromatic moiety enhances its stability and binding affinity, making it a preferred choice in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿7,650.00 |
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Ethyl 3-(4-fluorophenyl)-1H-pyrazole-5-carboxylate
This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring a pyrazole ring and a fluorophenyl group, makes it a valuable building block for developing compounds with potential therapeutic applications. Researchers often utilize it to create derivatives that are tested for anti-inflammatory, analgesic, and antimicrobial properties. Additionally, it plays a role in the development of pharmaceuticals targeting central nervous system disorders, owing to its ability to interact with specific biological receptors. Its fluorinated aromatic moiety enhances its stability and binding affinity, making it a preferred choice in drug discovery and development processes.
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