4-Chloroquinolin-8-amine
≥95%
- Product Code: 119198
CAS:
81764-16-1
| Molecular Weight: | 178.62 g./mol | Molecular Formula: | C₉H₇ClN₂ |
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| EC Number: | MDL Number: | MFCD18448245 | |
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| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
4-Chloroquinolin-8-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 agents, where it serves as a building block for creating derivatives that target the Plasmodium parasite. Additionally, it finds application in the research and development of anticancer drugs, as its quinoline core can be modified to interact with specific biological pathways involved in tumor growth and proliferation. The compound is also explored for its potential in designing anti-inflammatory and antimicrobial agents, leveraging its ability to inhibit enzymes or disrupt microbial cell processes. Its versatility in organic synthesis makes it a crucial component in the discovery of new therapeutic molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $192.11 |
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| 1.000 | 10-20 days | $535.66 |
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4-Chloroquinolin-8-amine
4-Chloroquinolin-8-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 agents, where it serves as a building block for creating derivatives that target the Plasmodium parasite. Additionally, it finds application in the research and development of anticancer drugs, as its quinoline core can be modified to interact with specific biological pathways involved in tumor growth and proliferation. The compound is also explored for its potential in designing anti-inflammatory and antimicrobial agents, leveraging its ability to inhibit enzymes or disrupt microbial cell processes. Its versatility in organic synthesis makes it a crucial component in the discovery of new therapeutic molecules.
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