Ethyl 5-amino-1-(3-fluorophenyl)-1H-pyrazole-4-carboxylate
95%
- Product Code: 84088
CAS:
138907-70-7
| Molecular Weight: | 249.24 g./mol | Molecular Formula: | C₁₂H₁₂FN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13176482 | |
| Melting Point: | Boiling Point: | 388.7±32.0 °C(Predicted) | |
| Density: | 1.33±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, keep away from light, dry and sealed |
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 a pyrazole core, makes it a valuable building block for developing compounds with potential therapeutic applications. Researchers often employ it in the design and synthesis of novel drugs targeting specific enzymes or receptors, particularly in the areas of anti-inflammatory, anticancer, and antimicrobial agents. Additionally, its fluorophenyl group enhances its ability to interact with biological targets, improving the pharmacokinetic properties of the resulting drug candidates. Its role in drug discovery underscores its importance in advancing pharmaceutical research and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,240.00 |
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| 0.250 | 10-20 days | ฿5,184.00 |
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| 1.000 | 10-20 days | ฿10,926.00 |
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Ethyl 5-amino-1-(3-fluorophenyl)-1H-pyrazole-4-carboxylate
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 a pyrazole core, makes it a valuable building block for developing compounds with potential therapeutic applications. Researchers often employ it in the design and synthesis of novel drugs targeting specific enzymes or receptors, particularly in the areas of anti-inflammatory, anticancer, and antimicrobial agents. Additionally, its fluorophenyl group enhances its ability to interact with biological targets, improving the pharmacokinetic properties of the resulting drug candidates. Its role in drug discovery underscores its importance in advancing pharmaceutical research and development.
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