7-(3-Chloropropoxy)-4-((2,4-dichloro-5-methoxyphenyl)amino)-6-methoxyquinoline-3-carbonitrile
97%
- Product Code: 53886
CAS:
380844-49-5
Molecular Weight: | 466.75 g./mol | Molecular Formula: | C₂₁H₁₈Cl₃N₃O₃ |
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EC Number: | MDL Number: | MFCD09833975 | |
Melting Point: | Boiling Point: | 585.6°C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a potential therapeutic agent. Its structure suggests it may act as a kinase inhibitor, making it a candidate for targeting specific enzymes involved in cellular signaling pathways. This application is particularly relevant in the development of treatments for cancers and other diseases where kinase activity is dysregulated.
Additionally, its quinoline core and functional groups indicate potential antimicrobial properties, which could be explored for combating resistant bacterial or fungal infections. Researchers may also investigate its use in biochemical assays to study enzyme mechanisms or as a molecular probe in cellular studies. Its precise application often depends on further pharmacological and toxicological evaluations to determine its efficacy and safety profile.
Product Specification:
Test | Specification |
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APPEARANCE | Yellow Solid |
PURITY | 96.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $53.48 |
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0.250 | 10-20 days | $99.10 |
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7-(3-Chloropropoxy)-4-((2,4-dichloro-5-methoxyphenyl)amino)-6-methoxyquinoline-3-carbonitrile
This compound is primarily utilized in the field of medicinal chemistry as a potential therapeutic agent. Its structure suggests it may act as a kinase inhibitor, making it a candidate for targeting specific enzymes involved in cellular signaling pathways. This application is particularly relevant in the development of treatments for cancers and other diseases where kinase activity is dysregulated.
Additionally, its quinoline core and functional groups indicate potential antimicrobial properties, which could be explored for combating resistant bacterial or fungal infections. Researchers may also investigate its use in biochemical assays to study enzyme mechanisms or as a molecular probe in cellular studies. Its precise application often depends on further pharmacological and toxicological evaluations to determine its efficacy and safety profile.
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