Imidazo[1,2-b]pyridazine-3-carbaldehyde
95%
- Product Code: 52686
CAS:
154578-27-5
| Molecular Weight: | 147.1341 g./mol | Molecular Formula: | C₇H₅N₃O |
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| Density: | Storage Condition: | room temperature |
Product Description:
Imidazo[1,2-b]pyridazine-3-carbaldehyde is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure serves as a building block for the development of potential drug candidates, particularly in the design of molecules targeting specific enzymes or receptors. Researchers often employ it in the creation of heterocyclic compounds that exhibit therapeutic properties, such as anti-inflammatory, anticancer, or antimicrobial activities. Additionally, its reactive aldehyde group makes it a versatile precursor for further chemical modifications, enabling the exploration of diverse pharmacological applications. This compound is also of interest in the study of structure-activity relationships (SAR) to optimize drug efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $80.36 |
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Imidazo[1,2-b]pyridazine-3-carbaldehyde
Imidazo[1,2-b]pyridazine-3-carbaldehyde is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure serves as a building block for the development of potential drug candidates, particularly in the design of molecules targeting specific enzymes or receptors. Researchers often employ it in the creation of heterocyclic compounds that exhibit therapeutic properties, such as anti-inflammatory, anticancer, or antimicrobial activities. Additionally, its reactive aldehyde group makes it a versatile precursor for further chemical modifications, enabling the exploration of diverse pharmacological applications. This compound is also of interest in the study of structure-activity relationships (SAR) to optimize drug efficacy and selectivity.
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