3-ethyl 5-(4-nitrobenzyl) 6,7-dihydropyrazolo[1,5-a]pyrazine-3,5(4H)-dicarboxylate
95%
- Product Code: 84051
CAS:
623565-15-1
| Molecular Weight: | 374.3473 g./mol | Molecular Formula: | C₁₇H₁₉N₄O₆ |
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| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents targeting specific enzymes or receptors, often in the context of neurological or cardiovascular research. The nitrobenzyl group enhances its reactivity, making it suitable for further chemical modifications to create potential drug candidates. Additionally, its pyrazolo[1,5-a]pyrazine core is frequently explored for its potential in designing compounds with anti-inflammatory, antimicrobial, or antitumor properties. Researchers also leverage its unique scaffold to study structure-activity relationships, aiding in the optimization of drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | ฿19,485.00 |
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| 1.000 | 10-20 days | ฿35,073.00 |
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3-ethyl 5-(4-nitrobenzyl) 6,7-dihydropyrazolo[1,5-a]pyrazine-3,5(4H)-dicarboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure is particularly valuable in the development of pharmaceutical agents targeting specific enzymes or receptors, often in the context of neurological or cardiovascular research. The nitrobenzyl group enhances its reactivity, making it suitable for further chemical modifications to create potential drug candidates. Additionally, its pyrazolo[1,5-a]pyrazine core is frequently explored for its potential in designing compounds with anti-inflammatory, antimicrobial, or antitumor properties. Researchers also leverage its unique scaffold to study structure-activity relationships, aiding in the optimization of drug efficacy and selectivity.
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