119474-39-4

Upstream product

• 75-15-0 carbon disulfide 
• 3862-73-5 2,3,4-trifluoroaniline 
• 121-44-8 triethylamine 

Downstream Products

• 119474-33-8 diethyl <(2,3,4-trifluoroanilino)<(4-methoxybenzyl)thio>methylene>malonate 
• 119474-34-9 ethyl 4-hydroxy-2-<(4-methoxybenzyl)thio>-6,7,8-trifluoroquinoline-3-carboxylate 
• 132305-92-1 4-(chloromethyl)-3-(2,3,4-trifluorophenyl)-2-(3H)-thiazolethione 
• 132305-67-0 9,1-methyliminomethano-7-fluoro-8-(4-methyl-1-piperazinyl)-5-oxo-5H-thiazolo<3,2-a>quinoline-4-carboxylic acid 
• 132305-91-0 3-chloro-2-oxopropyl N-(2,3,4-trifluorophenyl)-dithiocarbamate 
• 119474-40-7 2,3,4-trifluorophenyl isothiocyanate 

Relevant academic research and scientific papers

Studies on pyridonecarboxylic acids. III. Synthesis and antibacterial activity evaluation of 1,8-disubstituted 6-fluoro-4-oxo-7-piperazinyl-4H-[1,3]thiazeto[3,2-a] quinoline-3-carboxylic acid derivatives

A series of 1,8-disubstituted 6-fluoro-4-oxo-7-piperazinyl-4H-[1,3]thiazeto[3,2-a] quinoline-3-carboxylic acid derivatives was prepared and evaluated for antibacterial activity. In the 7-piperazinyl series, addition of a fluorine at C-8, which increased t

Synthesis and antibacterial activity of new tetracyclic quinolone antibacterials

A series of 8-substituted-9,1-(epoxymethano)-7-fluoro-5-oxo-5H- thiazolo[3,2-a]quinoline-4-carboxylic acids having a novel tetracyclic structure was synthesized and tested for antibacterial activity. The nature of the heteroatom (N, O, or S) substituted a