Ethyl 4-hydroxy-6-(trifluoromethoxy)quinoline-3-carboxylate

≥95%

Reagent Code: #47833
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CAS Number 175203-85-7

science Other reagents with same CAS 175203-85-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.22 g/mol
Formula C₁₃H₁₀F₃NO₄
badge Registry Numbers
MDL Number MFCD00219847
thermostat Physical Properties
Boiling Point 357.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a quinoline core with trifluoromethoxy and ester functional groups, makes it a versatile building block for developing potential pharmaceutical agents. It is particularly explored in the design of compounds targeting neurological disorders, inflammation, and infectious diseases due to its ability to interact with specific biological targets. Additionally, its trifluoromethoxy group enhances metabolic stability and bioavailability, making it valuable in drug discovery and development processes. Researchers also investigate its potential as a precursor for creating fluorescent probes or imaging agents in biochemical studies.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10g
10-20 days ฿2,592.00
5g
10-20 days ฿1,341.00
1g
10-20 days ฿288.00
25g
10-20 days ฿5,175.00
Ethyl 4-hydroxy-6-(trifluoromethoxy)quinoline-3-carboxylate
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This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a quinoline core with trifluoromethoxy and ester functional groups, makes it a versatile building block for developing potential pharmaceutical agents. It is particularly explored in the design of compounds targeting neurological disorders, inflammation, and infectious diseases due to its ability to interact with specific biological targets. Additionally, its trifluoromethoxy group enhances metabolic stability and bioavailability, making it valuable in drug discovery and development processes. Researchers also investigate its potential as a precursor for creating fluorescent probes or imaging agents in biochemical studies.
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