Thermotropic polyesters have been prepared from trans-1,4-cyclohexanedicarbonyl chloride and , -alkanediyl 4-hydroxybenzoates with a variable number of methylene carbons in the alkane chain. The melt transitions generally are lower than those of the corresponding thermotropic fully aromatic triad polyesters. The presence of cycloaliphatic groups in the mesogenic triad leads to enhanced solubility which has allowed an estimation, by GPC measurements, of the molecular weights which are rather low, corresponding to degrees of polymerization of no more than 3 or 4. The inherent viscosities for the polymers, however, are comparable to values published for other thermotropic polyesters with flexible spacers. For a polyester prepared from trans-1,4-cyclohexanedicarbonyl chloride and 4-hydroxybenzoic acid trans-1,4-cyclohexanediylbis-(methylene) ester no mesophase could be observed upon melting.