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The preferred hydrogen-bonding patterns in eight crystal structures of 2-thiouracil derivatives were analysed. In five of the structures, the usual pairs of N—H...S or N—H...O hydrogen bonds are formed, whereas three structures contain `mixed' R22(8) patterns with one N—H...S and one N—H...O hydrogen bond.

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The structures of eight benzoyl­hydrazones show similar conformations and hydrogen-bonding patterns. In most cases, the phenyl ring of the benzoyl group is rotated by about 30° with respect to the keto group. Only one of the amide groups exhibits the syn conformation.
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