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Ting Chen

Bio: Ting Chen is an academic researcher from Central China Normal University. The author has contributed to research in topics: Ring (chemistry). The author has an hindex of 1, co-authored 2 publications receiving 3 citations.

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TL;DR: In the title compound, C19H16Cl2NO5P, the P atom is in a distorted tetrahedral configuration, and the carboxylate plane is oriented almost perpendicular to the quinoline ring system.
Abstract: In the title compound, C19H16Cl2NO5P, the P atom is in a distorted tetra­hedral configuration, and the carboxyl­ate plane is oriented almost perpendicular to the quinoline ring system. In the crystal structure, mol­ecules are linked by inter­molecular C—H⋯O hydrogen bonds and weak π–π stacking inter­actions.

2 citations

Journal ArticleDOI
TL;DR: The asymmetric unit of the title compound, C23H23ClN4OS, contains two crystallographically independent molcules in which the orientations of the propylamine group and chloro-phenyl rings with respect to the fused ring system are different as mentioned in this paper.
Abstract: The asymmetric unit of the title compound, C23H23ClN4OS, contains two crystallographically independent mol­ecules in which the orientations of the propyl­amine group and chloro­phenyl rings with respect to the fused ring system are different. The terminal cyclo­hexene ring adopts a half-chair conformation. The crystal packing is stabilized by N—H⋯O, N—H⋯N and C—H⋯O hydrogen bonds and π–π inter­actions.

1 citations


Cited by
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TL;DR: In the title compound, C21H19N3O3S, the 5,6,7,8-tetrahydropyridine ring adopts a half-chair conformation and forms a dihedral angle of 2.66 (6)° with the attached phenyl ring.
Abstract: In the title compound, C21H19N3O3S, the 5,6,7,8-tetra­hydro­pyridine ring adopts a half-chair conformation. The fused-thieno[2,3-d]pyrimidine ring system is essentially planar (r.m.s. deviation = 0.001 A) and forms a dihedral angle of 2.66 (6)° with the attached phenyl ring. The three-dimensional crystal packing is stabilized by C—H⋯O and C—H⋯N hydrogen bonds and C—H⋯π inter­actions.

1 citations

Journal ArticleDOI
TL;DR: In this article, 14 phosphonates containing quinoline were synthesized and the preliminary bioassay indicated that these compounds exhibited a little better fungicidal and lower herbicidal activities than the starting compound Quinclorac.
Abstract: Fourteen of phosphonates containing quinoline were synthesized and the preliminary bioassay indicated that these compounds exhibited a little better fungicidal and lower herbicidal activities than the starting compound Quinclorac.
Journal ArticleDOI
TL;DR: The title compound, C12H9Cl2NO2, was prepared by the esterification of 3,7-dichloroquinoline-8-carboxylic acid with triethyl phosphite by stabilized by aromatic π–π stacking between the benzene and the pyridine rings of neighbouring molecules.
Abstract: The title compound, C12H9Cl2NO2, was prepared by the esterification of 3,7-dichloro­quinoline-8-carboxylic acid with triethyl phosphite. The crystal structure is stabilized by aromatic π–π stacking between the benzene and the pyridine rings of neighbouring mol­ecules [centroid–centroid distances = 3.716 (2) and 3.642 (2) A]. In addition, weak inter­molecular C—H⋯N hydrogen bonds are present in the structure.