Methyl 4-hydroxy-6-(trifluoromethyl)quinoline-2-carboxylate

95%

Reagent Code: #207057
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CAS Number 123158-31-6

science Other reagents with same CAS 123158-31-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.19 g/mol
Formula C₁₂H₈F₃NO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, this compound contributes to the development of antimicrobial agents with enhanced activity against resistant bacterial strains. Its structure supports the optimization of pharmacokinetic properties in final drug formulations. It is also employed in research settings for developing novel kinase inhibitors and other biologically active quinoline derivatives. The presence of the trifluoromethyl and hydroxy groups allows for further chemical modifications, making it valuable in medicinal chemistry and pharmaceutical development.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,510.00
inventory 250mg
10-20 days ฿4,570.00
Methyl 4-hydroxy-6-(trifluoromethyl)quinoline-2-carboxylate
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Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, this compound contributes to the development of antimicrobial agents with enhanced activity against resistant bacterial strains. Its structure supports the optimization of pharmacokinetic properties in final drug formulations. It is also employed in research settings for developing novel kinase inhibitors and other biologically active quinoline derivatives. The presence of the trifluoromethyl and hydroxy groups allows for further

Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, this compound contributes to the development of antimicrobial agents with enhanced activity against resistant bacterial strains. Its structure supports the optimization of pharmacokinetic properties in final drug formulations. It is also employed in research settings for developing novel kinase inhibitors and other biologically active quinoline derivatives. The presence of the trifluoromethyl and hydroxy groups allows for further chemical modifications, making it valuable in medicinal chemistry and pharmaceutical development.

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