125290-70-2

Upstream product

• 917-64-6 methyl magnesium iodide 
• 90619-70-8 2-(pentafluorophenyl)-4,4-dimethyl-2-oxazoline 
• 90619-69-5 2-(F-phenyl)-4,4-dimethyl-2-oxazoline hydrochloride 
• 90626-59-8 2-(F-benzoylamino)-2-methyl-1-propanol 
• 2251-50-5 pentafluorobenzoylchloride 
• 917-54-4 methyllithium 

Downstream Products

• 119915-88-7 1-(2,4-difluorophenyl)-6,7,8-trifluoro-1,4-dihydro-5-methyl-4-oxo-3-quinolinecarboxylic acid 
• 119915-51-4 ethyl α-(ethoxymethylene)-2,3,4,5-tetrafluoro-6-methyl-β-oxobenzenepropanoate 
• 119915-50-3 ethyl 2,3,4,5-tetrafluoro-6-methyl-β-oxobenzenepropanoate 
• 119915-48-9 2,3,4,5-tetrafluoro-6-methylbenzoyl chloride 
• 57612-65-4 2,3,4,5-tetrafluoro-6-methylbenzoic acid 

Relevant academic research and scientific papers

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

ORTHO-DISUBSTITUTED F-BENZENES - V. INTRAMOLECULAR HETEROATOM-FACILITATED ORTHO-SUBSTITUTION OF F-BENZENE DERIVATIVES WITH OXAZOLINYL AND OXAZINYL GROUPS.

The oxazinyl and oxazolinyl substituents on an F-benzene ring facilitated the substitution of fluorine ortho to the heterocyclic functional groups by carbon and nitrogen nucleophiles. Alkylmagnesium halides and alkyllithium compounds were employed as the