11-Chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline
95%
- Product Code: 114973
CAS:
5778-71-2
| Molecular Weight: | 231.72 g./mol | Molecular Formula: | C₁₄H₁₄ClN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11849287 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of more complex molecules. Its structure, featuring a fused cyclohepta[b]quinoline core, makes it valuable for constructing pharmacologically active compounds, particularly in the design of drugs targeting neurological disorders. Researchers often employ it in the synthesis of analogs that exhibit potential therapeutic effects, such as anti-inflammatory, antiviral, or anticancer properties. Additionally, its chlorinated moiety provides a reactive site for further chemical modifications, enabling the creation of diverse derivatives for biological screening and drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft79,318.98 |
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| 0.250 | 10-20 days | Ft118,978.47 |
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| 1.000 | 10-20 days | Ft297,300.74 |
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11-Chloro-7,8,9,10-tetrahydro-6H-cyclohepta[b]quinoline
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of more complex molecules. Its structure, featuring a fused cyclohepta[b]quinoline core, makes it valuable for constructing pharmacologically active compounds, particularly in the design of drugs targeting neurological disorders. Researchers often employ it in the synthesis of analogs that exhibit potential therapeutic effects, such as anti-inflammatory, antiviral, or anticancer properties. Additionally, its chlorinated moiety provides a reactive site for further chemical modifications, enabling the creation of diverse derivatives for biological screening and drug discovery efforts.
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