Abstract
In the title compound, C6H6Cl2N2O2S, the O atoms of the sulfonamide group lie on one side of the benzene ring and the amino group lies on the opposite side. An intermolecular N—H⋯Cl interaction occurs. In the crystal, adjacent molecules are linked by N—H⋯O hydrogen bonds, forming a three-dimensional structure with supporting π–π stacking interactions [centroid–centroid distance = 3.7903 (12) Å]. A short Cl⋯Cl contact [3.3177 (10) Å] also occurs.
Highlights
In the title compound, C6H6Cl2N2O2S, the O atoms of the sulfonamide group lie on one side of the benzene ring and the amino group lies on the opposite side
H atoms treated by a mixture of independent and constrained refinement max = 0.45 e Å3
Symmetry codes: (i) −x+1, −y+1, −z+1; (ii) x−1, −y+1/2, z−1/2; (iii) x, −y+1/2, z−1/2
Summary
H atoms treated by a mixture of independent and constrained refinement max = 0.45 e Å3. Key indicators: single-crystal X-ray study; T = 93 K; mean (C–C) = 0.002 Å; R factor =. 0.029; wR factor = 0.074; data-to-parameter ratio = 15.0. C6H6Cl2N2O2S, the O atoms of the sulfonamide group lie on one side of the benzene ring and the amino group lies on the opposite side. Adjacent molecules are linked by N—H O hydrogen bonds, forming a threedimensional structure with supporting – stacking interactions [centroid–centroid distance = 3.7903 (12) Å]. Cl Cl contact [3.3177 (10) Å] occurs
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