2-((3-(Ethoxycarbonyl)-6-(trifluoromethoxy)quinolin-4-yl)amino)benzoic acid

98%

Reagent Code: #184824
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CAS Number 384859-58-9

science Other reagents with same CAS 384859-58-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 420.345 g/mol
Formula C₂₀H₁₅F₃N₂O₅
badge Registry Numbers
MDL Number MFCD02932975
thermostat Physical Properties
Boiling Point 494.3±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.448±0.06 g/cm3(Predicted)
Storage Room temperature, inert gas

description Product Description

Used as a key intermediate in the synthesis of tyrosine kinase inhibitors, particularly in anticancer drug development. It plays a role in targeting signaling pathways involved in tumor growth and proliferation, especially in therapies directed against certain types of leukemia and solid tumors. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in research settings for developing novel quinoline-based pharmaceuticals with improved metabolic stability and bioavailability.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿9,920.00
inventory 50mg
10-20 days ฿19,660.00
inventory 100mg
10-20 days ฿31,550.00

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2-((3-(Ethoxycarbonyl)-6-(trifluoromethoxy)quinolin-4-yl)amino)benzoic acid
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Used as a key intermediate in the synthesis of tyrosine kinase inhibitors, particularly in anticancer drug development. It plays a role in targeting signaling pathways involved in tumor growth and proliferation, especially in therapies directed against certain types of leukemia and solid tumors. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in research settings for developing novel quinoline-based pharmaceuticals with improved metabolic stability a

Used as a key intermediate in the synthesis of tyrosine kinase inhibitors, particularly in anticancer drug development. It plays a role in targeting signaling pathways involved in tumor growth and proliferation, especially in therapies directed against certain types of leukemia and solid tumors. Its structure enables selective binding to enzyme active sites, enhancing drug efficacy. Also employed in research settings for developing novel quinoline-based pharmaceuticals with improved metabolic stability and bioavailability.

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