7-Methoxyquinolin-6-amine
95%
- Product Code: 54442
CAS:
1356016-60-8
| Molecular Weight: | 174.20 g./mol | Molecular Formula: | C₁₀H₁₀N₂O |
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| EC Number: | MDL Number: | MFCD23161396 | |
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| Density: | Storage Condition: | room temperature |
Product Description:
7-Methoxyquinolin-6-amine is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active compounds. Its structure is particularly valuable in the development of antimalarial drugs, where it serves as a precursor for creating molecules that target the Plasmodium parasite. Additionally, this compound is explored in the design of anticancer agents due to its ability to interact with specific cellular pathways involved in tumor growth and proliferation. Researchers also investigate its potential in developing anti-inflammatory and antimicrobial agents, leveraging its quinoline scaffold to enhance biological activity and selectivity. Its versatility makes it a valuable building block in drug discovery and development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,814.00 |
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| 0.250 | 10-20 days | ฿9,702.00 |
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| 1.000 | 10-20 days | ฿25,902.00 |
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7-Methoxyquinolin-6-amine
7-Methoxyquinolin-6-amine is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmacologically active compounds. Its structure is particularly valuable in the development of antimalarial drugs, where it serves as a precursor for creating molecules that target the Plasmodium parasite. Additionally, this compound is explored in the design of anticancer agents due to its ability to interact with specific cellular pathways involved in tumor growth and proliferation. Researchers also investigate its potential in developing anti-inflammatory and antimicrobial agents, leveraging its quinoline scaffold to enhance biological activity and selectivity. Its versatility makes it a valuable building block in drug discovery and development processes.
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