154257-75-7Relevant articles and documents
Synthesis method of 3-chloro-2,4-difluorobenzoic acid
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Paragraph 0023; 0030; 0031; 0032, (2017/02/17)
The invention relates to a synthesis method of 3-chloro-2,4-difluorobenzoic acid. The method comprises: taking 1,2,3-trichlorobenzene and N-bromosuccinimide to react, taking CuCN and 1-bromo-2,3,4-trichlorobenzene to react, taking the 1-bromo-2,3,4-trichlorobenzene and KF to react and taking 3-chloro-2,4-difluorobenzonitrile and sulfuric acid to react, so as to form the 3-chloro-2,4-difluorobenzoic acid. According to the synthesis method, synthesis reaction conditions are that a reaction is carried out at normal pressure and reaction temperature fluctuates between 0 and 250 DEG C; the obtained finished product is a light yellow powdery solid and the content is more than or equal to 99.0 percent; the total mol yield of the 3-chloro-2,4-difluorobenzoic acid can reach 61.5 percent; whole reaction conditions are moderate and the method is convenient to operate and control; pressure of waste gas, waste water and waste residues is relatively low so that industrial production is facilitated.
ANTIMICROBIAL QUINOLONES, THEIR COMPOSITIONS AND USES
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Page 79; 80, (2010/02/06)
Compounds of the following formula (I) are effective antimicrobial agents.
Antimicrobial quinolones, their compositions and uses
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, (2008/06/13)
Compounds having the general structure: which are effective antimicrobial agents.