3-(Pyridin-3-yl)-1H-pyrazole-5-carboxylic acid
97%
- Product Code: 119774
CAS:
374064-01-4
| Molecular Weight: | 189.17 g./mol | Molecular Formula: | C₉H₇N₃O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05170031 | |
| Melting Point: | Boiling Point: | 541.4°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
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 pyridine and pyrazole rings, makes it a versatile building block for developing compounds with potential therapeutic applications. Researchers often employ it in the design and synthesis of inhibitors targeting specific enzymes or receptors, particularly in the context of anti-inflammatory, anticancer, and antimicrobial drug development. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological properties. Its role in the development of novel drug candidates underscores its importance in pharmaceutical research and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿756.00 |
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| 0.250 | 10-20 days | ฿1,026.00 |
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| 1.000 | 10-20 days | ฿2,538.00 |
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| 5.000 | 10-20 days | ฿8,163.00 |
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3-(Pyridin-3-yl)-1H-pyrazole-5-carboxylic acid
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 pyridine and pyrazole rings, makes it a versatile building block for developing compounds with potential therapeutic applications. Researchers often employ it in the design and synthesis of inhibitors targeting specific enzymes or receptors, particularly in the context of anti-inflammatory, anticancer, and antimicrobial drug development. Additionally, its carboxylic acid group allows for further functionalization, enabling the creation of derivatives with enhanced pharmacological properties. Its role in the development of novel drug candidates underscores its importance in pharmaceutical research and development.
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