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The conformation of the title mol­ecule, C17H17N3S, is stabilized by an intra­molecular N-H...N hydrogen bond involving the azometinic group. The dihedral angle between the two aromatic rings is 36.49 (06)°. The non-aromatic ring of the tetra­lone substituent adopts a sofa conformation. In the crystal, mol­ecules are linked by pairs of N-H...S hydrogen bonds related via centres of symmetry, forming dimers.

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This page is a summary of: N-Phenyl-2-(1,2,3,4-tetrahydronaphthalen-1-ylidene)hydrazinecarbothioamide, Acta Crystallographica Section E Structure Reports Online, January 2014, International Union of Crystallography,
DOI: 10.1107/s1600536814001585.
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