Fig. 4From: Atypical bromethalin intoxication in a dog: pathologic features and identification of an isomeric breakdown productLikely origin of the two different 543.7 MW (nominal MW 541) bromethalin breakdown products as dehydrofluorodesmethylbromethalin structures of formula C13H4N3O4F2Br3. The compounds have been given common names of dehydrofluorodesmethylbromethalin-I and –II, which would be 6-(difluoromethylene)-2,4-dinitro-N-(2,4,6-tribromophenyl)cyclohexa-2,4-dien-1-imine and 8,8-difluoro-3,5-dinitro-(2,4,6-tribromophenyl)-7-azabicyclo[4.2.0]octa-1,3,5-triene, respectively. Dehydrofluorobromethalin (3,3-difluoro-5,7-dinitro-1-(2,4,6-tribromophenyl)indoline) was not seen and its absence is significant in light of the apparent lack of formation of a five member ring in deference to a more constrained four member ringBack to article page