N-(5-Chloro-2-nitrophenyl)-2,2-dimethylpropanamide
نویسندگان
چکیده
منابع مشابه
Supramolecular structures of three isomeric 2-chloro-N-(nitrophenyl)nicotinamides.
Molecules of 2-chloro-N-(2-nitrophenyl)nicotinamide, C12H8ClN3O3, are linked by two C-H...O hydrogen bonds into a chain of edge-fused R(2)(2) (14) and (4)(4) (24) rings. In 2-chloro-N-(3-nitrophenyl)nicotinamide monohydrate, C12H8ClN3O3.H2O, the molecules are linked by a combination of N-H...O, O-H...O and O-H...N hydrogen bonds into a chain of edge-fused rings containing two distinct types of ...
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The title Schiff base compound, C(15)H(13)ClN(2)O(3), was prepared by the reaction of equimolar quanti-ties of 5-chloro-2-hy-droxy-benzaldehyde with 2-meth-oxy-benzohydrazide in a methanol solution. The dihedral angle between the two benzene rings is 20.6 (3)°. An intra-molecular O-H⋯N hydrogen bond may influence the mol-ecular conformation. In the crystal structure, mol-ecules form chains alon...
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In the title compound, C(11)H(12)ClNO(3), the conformation of the N-H bond in the amide segment is syn with respect to the ortho-Cl atom. The amide and carboxyl C=O groups are syn to each other. Furthermore, the C=O and O-H bonds of the carboxyl group are in syn positions with respect to each other. The dihedral angle between the benzene ring and the amide group is 47.8 (2)°. In the crystal, mo...
متن کاملN-(5-Chloro-2-nitrophenyl)-2,2-dimethylpropanamide
In the crystal structure of the title compound, C(11)H(13)ClN(2)O(3), mol-ecules are linked through C-H⋯O hydrogen bonds.
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In the title compound, C(13)H(12)ClNO(3)S, the dihedral angle between the two aromatic rings is 73.94 (9)°. An intra-molecular C-H⋯O hydrogen bond occurs. In the crystal, inter-molecular N-H⋯O hydrogen bonds connect the mol-ecules to centrosymmetric dimers, forming an R(2) (2)(8) ring motif. The packing is consolidated by C-H⋯O hydrogen bonds and weak π-π inter-actions [centroid-centroid distan...
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ژورنال
عنوان ژورنال: Acta Crystallographica Section E Structure Reports Online
سال: 2012
ISSN: 1600-5368
DOI: 10.1107/s1600536812027730