1-Benzoyl-N-phenylcyclopropanecarboxamide

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منابع مشابه

1-Benzoyl-N-phenyl­cyclo­propane­carboxamide

The title compound, C(17)H(15)NO(2), was synthesized by reaction of 1,2-dibromo-ethane with 1-benzoyl-N-phenyl-cyclo-propane-carboxamide and K(2)CO(3) in dimethyl-formamide. The mol-ecule exhibits a V-shaped conformation in the crystal with a dihedral angle of 88.7 (3)° between the two benzene rings. Pairs of N-H⋯O hydrogen bonds link the mol-ecules into dimers about centres of inversion.

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1-Benzoyl-3-(4-n-butyl­phen­yl)thio­urea

The dihedral angle between the benzoyl and phenyl groups in the title compound, C(18)H(20)N(2)OS, is 30.57 (4)°. The crystal packing is characterized by N-H⋯O hydrogen bonds. In the crysta, pairs of N-H⋯S hydrogen bonds link the molecules into inversion dimers.

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N-Benzoyl-N′-phenyl­urea

In the title compound, C(14)H(12)N(2)O(2), the mol-ecular conformation is determined by a strong intra-molecular N-H⋯O=C hydrogen bond. In the crystal, pairs of mol-ecules are connected by inter-molecular N-H⋯O=C hydrogen bonds, forming centrosymmetric dimers. No specific inter-actions between dimers could be found.

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N-Benzoyl-N′,N′-dimethyl­thio­urea

In the title compound, C(10)H(12)N(2)OS, the amide NCO group is twisted relative to the thio-ureido SCN(2) group, forming a dihedral angle of 55.3 (2)°. The crystal packing shows inter-molecular N-H⋯S and weak C-H⋯O inter-actions, the former giving rise to the formation of centrosymmetric R(2) (2)(8) dimers.

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4-Carbethoxy-1-[4-(N,N-dimethylamino)benzoyl]thiosemicarbazide

The mol-ecular structure of the title compound, C(13)H(18)N(4)O(3)S, (systematic name: ethyl N-{2-[4-(dimethyl-amino)benzo-yl]hydrazinethio-carbon-yl}carbamate) is stabilized by intra-molecular N-H⋯O=C hydrogen bonding arranged in an S(6) graph-set motif. In the crystal, inversion dimers connected via inter-molecular N-H⋯S=C hydrogen bonds [R(2) (2)(8) graph-set motif] form sheets parallel to t...

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ژورنال

عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online

سال: 2008

ISSN: 1600-5368

DOI: 10.1107/s1600536808034077