1,2-Dimethyl-4-oxo-6-(trifluoromethoxy)-1,4-dihydroquinoline-3-carboxylic acid

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Reagent Code: #123731
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CAS Number 1958082-61-5

science Other reagents with same CAS 1958082-61-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.22 g/mol
Formula C₁₃H₁₀F₃NO₄
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This compound is a key intermediate in medicinal chemistry, primarily used in the synthesis of quinolone-based pharmaceuticals, including antibacterial agents targeting microbial infections. Its core structure as a 1,4-dihydroquinoline-4-one-3-carboxylic acid derivative enables effective inhibition of bacterial DNA gyrase and topoisomerase IV. The trifluoromethoxy group at the 6-position enhances lipophilicity, metabolic stability, and biological potency. Additionally, it is explored for developing drugs addressing inflammatory and autoimmune diseases through interactions with relevant biological pathways, offering potential anti-inflammatory and immunomodulatory effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,528.00
inventory 100mg
10-20 days ฿1,413.00
inventory 1g
10-20 days ฿10,926.00

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1,2-Dimethyl-4-oxo-6-(trifluoromethoxy)-1,4-dihydroquinoline-3-carboxylic acid
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This compound is a key intermediate in medicinal chemistry, primarily used in the synthesis of quinolone-based pharmaceuticals, including antibacterial agents targeting microbial infections. Its core structure as a 1,4-dihydroquinoline-4-one-3-carboxylic acid derivative enables effective inhibition of bacterial DNA gyrase and topoisomerase IV. The trifluoromethoxy group at the 6-position enhances lipophilicity, metabolic stability, and biological potency. Additionally, it is explored for developing drugs

This compound is a key intermediate in medicinal chemistry, primarily used in the synthesis of quinolone-based pharmaceuticals, including antibacterial agents targeting microbial infections. Its core structure as a 1,4-dihydroquinoline-4-one-3-carboxylic acid derivative enables effective inhibition of bacterial DNA gyrase and topoisomerase IV. The trifluoromethoxy group at the 6-position enhances lipophilicity, metabolic stability, and biological potency. Additionally, it is explored for developing drugs addressing inflammatory and autoimmune diseases through interactions with relevant biological pathways, offering potential anti-inflammatory and immunomodulatory effects.

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