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The asymmetric unit of the title compound, C21H20N2S, comprises two independent mol­ecules, which differ in the conformations of the cyclo­hexene and di­hydro­pyrimidine rings, and in the orientations of the benzyl­idene moieties. The crystal structure is stabilized by weak N—H...S hydrogen bonds.

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The title compound, C20H14N2OS, was synthesized by mixing imidazolidine-2-thione, ethyl chloro­acetate and anthracene-10-carb­aldehyde in ethanol. The dihedral angle between the anthracene plane and the heterocyclic ring system is 61.5 (3)°. In the crystal structure, the mol­ecules are linked via weak C—H...O interactions.

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The title compound, C15H5Cl4NO3, was synthesized from tetra­chloro­phthalic anhydride and 4-amino­benz­aldehyde. In the mol­ecule, the tetra­chloro­phthal­imide unit is nearly planar and makes a dihedral angle of 56.20 (3)° with the benzene ring.

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The title compound, C13H10N2O2, is approximately planar in the solid state and displays a trans configuration with respect to the azo double bond. Molecules form infinite chains linked by O—H...O hydrogen bonds along the a axis.

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The title compound, C20H12N2OS, was synthesized by mixing 2,4-dichloro­benzaldehyde, ethyl chloro­acetate and tetra­hydro­pyrimidine-2-thione in ethanol. The dihedral angle between the naphthalene plane and the heterocyclic ring system is 9.3 (3)°.

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The crystal structure of the title compound, C17H12N2O2·C10H8O, shows that the mol­ecules are effectively planar in the solid state and the compound exists in the hydrazone form and not the azo form. The hydrazone H atom and carbonyl O atom are linked by an intra­molecular N—H...O hydrogen bond. The 2-naphthol molecules are disordered over inversion centres, the asymmetric unit containing half each of two such molecules. The packing can be described as a polymeric arrangement of mol­ecules linked through O—H...O hydrogen bonds.
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