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The title compound, C33H29N, was obtained by the reaction of 9-chloro­methyl­anthracene and n-propyl­amine. Two anthra­cenyl­methyl units are linked to the N atom of n-propyl­amine and the dihedral angle between the two anthracene systems is 64.3 (2)°.

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The title compound, C9H12N2O3, was synthesized by the reaction in ethanol of ethane-1,2-di­amine and 3-[bis­(methyl­thio)­methyl­ene]-6-methyl-3,4,5,6-tetra­hydro-2H-pyran-2,4-dione. Two intramolecular N—H...O hydrogen bonds induce a high degree of planarity.

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The title compound, C15H16N2O2S, which is a potentially new bioactive mol­ecule containing pyrazole and pyrone ring systems, was synthesized by the reaction of 1-p-tolyl­hydrazine and 3-[bis­(methyl­thio)methyl­ene]dihydro-6-meth­yl-3H-pyran-2,4-dione in ethanol.

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The title compound, C16H19N7, is a potent new herbicide. X-ray analysis reveals that the piperazine ring adopts a chair conformation and weak C—H...N hydrogen bonds link the mol­ecules into a chain along the a axis.

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The title compound, C18H20ClN3O2, is a potent new herbicide. X-ray analysis reveals that the benzene ring is twisted away from the isoxazole ring by 67.7 (1)°. The crystal packing is stabilized by inter­molecular N—H...N and C—H...O hydrogen bonds.

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The title compound, C14H19N3O7S, is a potent new herbicide. X-ray analysis reveals that the nitro group is twisted away from the benzene ring and the glutamine residue adopts a folded conformation. The crystal packing is stabilized by inter­molecular N—H...O and O—H...O hydrogen bonds.

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The title compound, C15H14N2O3S, a potent new bioactive mol­ecule which contains pyrazole and pyrone ring systems, was synthesized by the reaction of benzohydrazide and 3-[bis­(methyl­sulfan­yl)methyl­ene]dihydro-6-methyl-3H-pyran-[2,4-dione in ethanol.
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