8-Chloro-6,7-difluoro-1-((1R,2S)-2-fluorocyclopropyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

97%

Reagent Code: #160629
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CAS Number 127199-27-3

science Other reagents with same CAS 127199-27-3

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Weight 317.65 g/mol
Formula C₁₃H₇ClF₃NO₃
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the development of advanced antimicrobial agents targeting drug-resistant bacterial strains. Its structure enables enhanced penetration into bacterial cells and improved binding to DNA gyrase and topoisomerase IV, making it valuable in creating potent inhibitors. This compound is especially relevant in the design of next-generation antibiotics with broad-spectrum activity and reduced susceptibility to common resistance mechanisms. It is also employed in medicinal chemistry research to explore structure-activity relationships in quinolone-based therapeutics.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,840.00
inventory 100mg
10-20 days ฿4,440.00

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8-Chloro-6,7-difluoro-1-((1R,2S)-2-fluorocyclopropyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
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Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the development of advanced antimicrobial agents targeting drug-resistant bacterial strains. Its structure enables enhanced penetration into bacterial cells and improved binding to DNA gyrase and topoisomerase IV, making it valuable in creating potent inhibitors. This compound is especially relevant in the design of next-generation antibiotics with broad-spectrum activity and reduced susceptibility to common resis

Used as a key intermediate in the synthesis of fluoroquinolone antibiotics, particularly in the development of advanced antimicrobial agents targeting drug-resistant bacterial strains. Its structure enables enhanced penetration into bacterial cells and improved binding to DNA gyrase and topoisomerase IV, making it valuable in creating potent inhibitors. This compound is especially relevant in the design of next-generation antibiotics with broad-spectrum activity and reduced susceptibility to common resistance mechanisms. It is also employed in medicinal chemistry research to explore structure-activity relationships in quinolone-based therapeutics.

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