7-(Thiophen-2-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
95%
- Product Code: 87687
CAS:
676247-93-1
| Molecular Weight: | 245.26 g./mol | Molecular Formula: | C₁₁H₇N₃O₂S |
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| EC Number: | MDL Number: | MFCD04049989 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development due to its structural properties, which make it a promising candidate for the synthesis of biologically active molecules. Its pyrazolopyrimidine core is known to interact with various enzymes and receptors, making it valuable for designing inhibitors or modulators targeting specific pathways. Researchers often explore its derivatives for potential applications in treating diseases such as cancer, inflammation, or neurological disorders. Additionally, its thiophene moiety can enhance binding affinity and selectivity, contributing to its effectiveness in drug discovery. The compound's carboxylic acid group allows for further chemical modifications, enabling the creation of diverse analogs for structure-activity relationship studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft55,368.14 |
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| 0.250 | 10-20 days | Ft100,748.68 |
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| 1.000 | 10-20 days | Ft212,260.70 |
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7-(Thiophen-2-yl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry and drug development due to its structural properties, which make it a promising candidate for the synthesis of biologically active molecules. Its pyrazolopyrimidine core is known to interact with various enzymes and receptors, making it valuable for designing inhibitors or modulators targeting specific pathways. Researchers often explore its derivatives for potential applications in treating diseases such as cancer, inflammation, or neurological disorders. Additionally, its thiophene moiety can enhance binding affinity and selectivity, contributing to its effectiveness in drug discovery. The compound's carboxylic acid group allows for further chemical modifications, enabling the creation of diverse analogs for structure-activity relationship studies.
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