132630-83-2

Upstream product

• 88419-56-1 2,4,5-trifluorobenzoyl chloride 
• 446-17-3 2,4,5-trifluorobenzoic acid 
• 125290-72-4 2-(2,4,5-trifluorophenyl)-4,4-dimethyl-2-oxazoline 
• 74-88-4 methyl iodide 

Downstream Products

• 132630-84-3 2-(2,4,5-trifluoro-3,6-dimethylphenyl)-4,4-dimethyl-2-oxazoline 
• 132630-91-2 ethyl α-(ethoxymethylene)-2,4,5-trifluoro-3,6-dimethyl-β-oxobenzenepropanoate 
• 132630-88-7 ethyl 2,4,5-trifluoro-3,6-dimethyl-β-oxobenzenepropanoate 
• 178174-10-2 5-(Benzyl-methyl-amino)-1-cyclopropyl-6,7-difluoro-8-methyl-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester 
• 178174-05-5 2-Chloro-3,4,6-trifluoro-5-methyl-benzoic acid 2-acetylamino-2-methyl-propyl ester 
• 178174-07-7 ethyl 2-(6-chloro-3,4,5-trifluoro-2-methylbenzoyl)acetate 
• 1025916-28-2 2-Chloro-3,4,6-trifluoro-5-methyl-benzoyl chloride 
• 178174-06-6 2-chloro-3,4,6-trifluoro-5-methylbenzoic acid 
• 132630-87-6 3,6-dimethyl-2,4,5-trifluoro-benzoic acid 
• 112822-85-2 3-methyl-2,4,5-trifluorobenzoic acid 
• 178174-03-3 2-(2-Chloro-3,4,6-trifluoro-5-methyl-phenyl)-4,4-dimethyl-4,5-dihydro-oxazole 

Relevant academic research and scientific papers

Synthesis of mono- and di-substituted 2,4,5-trifluorobenzoic acid synthons, key precursors for biologically active 6-fluoroquinolones

In the search for new potent antiparasitical fluoroquinolones, a QSAR analysis by molecular connectivity led to the design of R5 (Me or Et)/R8 (MeO, Me or Et)-substituted analogs of the most powerful antibacterial or antiparasitical

Antibacterial agents

Novel naphthyridine-, and quinolinecarboxylic acids as antibacterial agents are described as well as methods for their manufacture, formulation, and use in treating bacterial infections including the description of certain novel intermediates used in the