Benzyl (1-(tert-butyl)-3-(3-oxocyclopentyl)-1H-pyrazol-5-yl)carbamate
98%
- Product Code: 124630
CAS:
2460255-78-9
| Molecular Weight: | 355.43 g./mol | Molecular Formula: | C₂₀H₂₅N₃O₃ |
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| Density: | Storage Condition: | 2-8°C, dry |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition or receptor modulation. Its structure, featuring a pyrazole ring and a cyclopentyl group, makes it a valuable scaffold for developing potential therapeutic agents. Researchers often employ it in the design and optimization of drug candidates for treating inflammatory diseases, cancer, or metabolic disorders. Its tert-butyl group enhances stability, while the carbamate moiety allows for further functionalization, making it versatile in drug discovery workflows. Additionally, it may be used in studies exploring structure-activity relationships (SAR) to improve the efficacy and selectivity of new drug molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,041.00 |
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| 1.000 | 10-20 days | ฿8,082.00 |
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| 5.000 | 10-20 days | ฿24,255.00 |
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Benzyl (1-(tert-butyl)-3-(3-oxocyclopentyl)-1H-pyrazol-5-yl)carbamate
This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting enzyme inhibition or receptor modulation. Its structure, featuring a pyrazole ring and a cyclopentyl group, makes it a valuable scaffold for developing potential therapeutic agents. Researchers often employ it in the design and optimization of drug candidates for treating inflammatory diseases, cancer, or metabolic disorders. Its tert-butyl group enhances stability, while the carbamate moiety allows for further functionalization, making it versatile in drug discovery workflows. Additionally, it may be used in studies exploring structure-activity relationships (SAR) to improve the efficacy and selectivity of new drug molecules.
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