The stereochemistry of 1,2,5,6,9,10-hexabromocyclododecane and its graphic representation

1,2,5,6,9,10-Hexabromocyclododecane, a widely used additive flame retardant, is produced by bromination of cis,trans,trans-cyclododeca-1,5,9-triene, resulting in a mixture of three enantiomeric pairs of diastereomers. We present here the correct configuration and graphic representation of the six isomers. Recently, the complete separation of all six isomers has been achieved using chiral liquid chromatography.