4-Hydroxy-7-(trifluoromethyl)quinoline-3-carboxylic acid

95%

Reagent Code: #196002
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CAS Number 574-92-5

science Other reagents with same CAS 574-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.17 g/mol
Formula C₁₁H₆F₃NO₃
badge Registry Numbers
MDL Number MFCD00006771
thermostat Physical Properties
Melting Point 259-260°C
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antibacterial and antiviral agents. Its structure supports metal chelation, making it useful in catalysis and in the design of enzyme inhibitors. Also employed in research for fluorescent probes due to its ability to form stable complexes with metal ions, enhancing luminescent properties. Commonly utilized in medicinal chemistry for structure-activity relationship studies targeting kinase inhibition and antimicrobial resistance.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,100.00
inventory 1g
10-20 days ฿2,400.00
inventory 5g
10-20 days ฿8,800.00
4-Hydroxy-7-(trifluoromethyl)quinoline-3-carboxylic acid
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Used as a key intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antibacterial and antiviral agents. Its structure supports metal chelation, making it useful in catalysis and in the design of enzyme inhibitors. Also employed in research for fluorescent probes due to its ability to form stable complexes with metal ions, enhancing luminescent properties. Commonly utilized in medicinal chemistry for structure-activity relationship studies targeting kinase in

Used as a key intermediate in the synthesis of quinolone-based pharmaceuticals, particularly in the development of antibacterial and antiviral agents. Its structure supports metal chelation, making it useful in catalysis and in the design of enzyme inhibitors. Also employed in research for fluorescent probes due to its ability to form stable complexes with metal ions, enhancing luminescent properties. Commonly utilized in medicinal chemistry for structure-activity relationship studies targeting kinase inhibition and antimicrobial resistance.

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