5-Amino-1-(4-fluorophenyl)-1H-pyrazole-4-carboxylic acid
97%
- Product Code: 119917
CAS:
187949-90-2
| Molecular Weight: | 221.19 g./mol | Molecular Formula: | C₁₀H₈FN₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01569434 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring a pyrazole ring and a carboxylic acid group, makes it a versatile building block for developing drugs with potential anti-inflammatory, analgesic, and antimicrobial properties. Researchers often utilize it to design and optimize molecules targeting specific enzymes or receptors, particularly in the development of treatments for neurological disorders or infectious diseases. Additionally, its fluorophenyl group enhances its binding affinity to biological targets, making it valuable in drug discovery and development processes.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Pale-yellow To Yellow-brown Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿680.00 |
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| 1.000 | 10-20 days | ฿1,580.00 |
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| 5.000 | 10-20 days | ฿5,600.00 |
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| 25.000 | 10-20 days | ฿21,840.00 |
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5-Amino-1-(4-fluorophenyl)-1H-pyrazole-4-carboxylic acid
This compound is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring a pyrazole ring and a carboxylic acid group, makes it a versatile building block for developing drugs with potential anti-inflammatory, analgesic, and antimicrobial properties. Researchers often utilize it to design and optimize molecules targeting specific enzymes or receptors, particularly in the development of treatments for neurological disorders or infectious diseases. Additionally, its fluorophenyl group enhances its binding affinity to biological targets, making it valuable in drug discovery and development processes.
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