4-Chloro-7-(3-chloropropoxy)-6-methoxyquinoline-3-carbonitrile
≥95%
- Product Code: 81314
CAS:
214470-68-5
| Molecular Weight: | 311.16 g./mol | Molecular Formula: | C₁₄H₁₂Cl₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09833974 | |
| Melting Point: | Boiling Point: | 478.1°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those with potential therapeutic applications. Its structure, featuring a quinoline core and functional groups like chloro, methoxy, and nitrile, makes it a versatile building block for developing compounds with biological activity. Researchers often explore its use in creating inhibitors or modulators for specific enzymes or receptors, which could be relevant in treating diseases such as cancer, infections, or inflammatory conditions. Additionally, its chemical properties allow for further derivatization, enabling the development of novel drug candidates with optimized efficacy and safety profiles.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,474.00 |
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| 0.250 | 10-20 days | ฿5,211.00 |
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| 1.000 | 10-20 days | ฿13,032.00 |
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| 5.000 | 10-20 days | ฿41,697.00 |
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4-Chloro-7-(3-chloropropoxy)-6-methoxyquinoline-3-carbonitrile
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules, particularly those with potential therapeutic applications. Its structure, featuring a quinoline core and functional groups like chloro, methoxy, and nitrile, makes it a versatile building block for developing compounds with biological activity. Researchers often explore its use in creating inhibitors or modulators for specific enzymes or receptors, which could be relevant in treating diseases such as cancer, infections, or inflammatory conditions. Additionally, its chemical properties allow for further derivatization, enabling the development of novel drug candidates with optimized efficacy and safety profiles.
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