3-nitropyrazolo[1,5-a]pyrimidin-5(4H)-one
98%
- Product Code: 87386
CAS:
1919868-75-9
| Molecular Weight: | 180.121 g./mol | Molecular Formula: | C₆H₄N₄O₃ |
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| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural properties. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its nitropyrazole moiety makes it a valuable scaffold for developing inhibitors of kinases and other enzymes involved in signaling pathways, which are crucial in treating diseases like cancer and inflammatory disorders. Additionally, it is explored for its potential in creating novel antimicrobial agents, given its ability to interact with bacterial or fungal enzymes. Researchers also investigate its use in designing compounds with potential antiviral or antiparasitic activities, leveraging its unique chemical structure to enhance drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,898.00 |
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| 1.000 | 10-20 days | ฿6,687.00 |
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| 5.000 | 10-20 days | ฿21,618.00 |
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3-nitropyrazolo[1,5-a]pyrimidin-5(4H)-one
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research due to its structural properties. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzyme inhibition. Its nitropyrazole moiety makes it a valuable scaffold for developing inhibitors of kinases and other enzymes involved in signaling pathways, which are crucial in treating diseases like cancer and inflammatory disorders. Additionally, it is explored for its potential in creating novel antimicrobial agents, given its ability to interact with bacterial or fungal enzymes. Researchers also investigate its use in designing compounds with potential antiviral or antiparasitic activities, leveraging its unique chemical structure to enhance drug efficacy and selectivity.
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