5-Chloro-1-(pyridin-2-yl)-1H-pyrazole-4-carbonitrile
≥95%
- Product Code: 119971
CAS:
104771-35-9
| Molecular Weight: | 204.62 g./mol | Molecular Formula: | C₉H₅ClN₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17168530 | |
| Melting Point: | Boiling Point: | 395°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds. Its structure is particularly valuable in the synthesis of heterocyclic compounds, which are often explored for their potential therapeutic properties. Researchers utilize it to create molecules that may exhibit antimicrobial, anti-inflammatory, or anticancer activities. Additionally, it is employed in the design and optimization of agrochemicals, contributing to the development of new pesticides or herbicides. Its versatility in chemical reactions makes it a valuable building block in medicinal chemistry and drug discovery processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | €36.33 |
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| 0.250 | 10-20 days | €54.14 |
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| 1.000 | 10-20 days | €135.58 |
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5-Chloro-1-(pyridin-2-yl)-1H-pyrazole-4-carbonitrile
This chemical is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds. Its structure is particularly valuable in the synthesis of heterocyclic compounds, which are often explored for their potential therapeutic properties. Researchers utilize it to create molecules that may exhibit antimicrobial, anti-inflammatory, or anticancer activities. Additionally, it is employed in the design and optimization of agrochemicals, contributing to the development of new pesticides or herbicides. Its versatility in chemical reactions makes it a valuable building block in medicinal chemistry and drug discovery processes.
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