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rac-3-[(3-Chloroanilino)(4-chlorophenyl)methyl]thian-4-one
In the title compound, C(18)H(17)Cl(2)NOS, the thiopyranone ring adopts a chair conformation, with the substituent in the axial position. The dihedral angle between the two benzene rings is 89.43 (1)°. In the crystal, molecules form inversion dimers through intermolecular N—H⋯O hydrogen bonds [g...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295438/ https://www.ncbi.nlm.nih.gov/pubmed/22412549 http://dx.doi.org/10.1107/S1600536812004680 |
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author | Harms, Klaus Abaee, M. Saeed Mojtahedi, Mohammad M. Mesbah, A. Wahid |
author_facet | Harms, Klaus Abaee, M. Saeed Mojtahedi, Mohammad M. Mesbah, A. Wahid |
author_sort | Harms, Klaus |
collection | PubMed |
description | In the title compound, C(18)H(17)Cl(2)NOS, the thiopyranone ring adopts a chair conformation, with the substituent in the axial position. The dihedral angle between the two benzene rings is 89.43 (1)°. In the crystal, molecules form inversion dimers through intermolecular N—H⋯O hydrogen bonds [graph set R (2) (2)(8)]. |
format | Online Article Text |
id | pubmed-3295438 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32954382012-03-12 rac-3-[(3-Chloroanilino)(4-chlorophenyl)methyl]thian-4-one Harms, Klaus Abaee, M. Saeed Mojtahedi, Mohammad M. Mesbah, A. Wahid Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(17)Cl(2)NOS, the thiopyranone ring adopts a chair conformation, with the substituent in the axial position. The dihedral angle between the two benzene rings is 89.43 (1)°. In the crystal, molecules form inversion dimers through intermolecular N—H⋯O hydrogen bonds [graph set R (2) (2)(8)]. International Union of Crystallography 2012-02-10 /pmc/articles/PMC3295438/ /pubmed/22412549 http://dx.doi.org/10.1107/S1600536812004680 Text en © Harms et al. 2012 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Harms, Klaus Abaee, M. Saeed Mojtahedi, Mohammad M. Mesbah, A. Wahid rac-3-[(3-Chloroanilino)(4-chlorophenyl)methyl]thian-4-one |
title |
rac-3-[(3-Chloroanilino)(4-chlorophenyl)methyl]thian-4-one |
title_full |
rac-3-[(3-Chloroanilino)(4-chlorophenyl)methyl]thian-4-one |
title_fullStr |
rac-3-[(3-Chloroanilino)(4-chlorophenyl)methyl]thian-4-one |
title_full_unstemmed |
rac-3-[(3-Chloroanilino)(4-chlorophenyl)methyl]thian-4-one |
title_short |
rac-3-[(3-Chloroanilino)(4-chlorophenyl)methyl]thian-4-one |
title_sort | rac-3-[(3-chloroanilino)(4-chlorophenyl)methyl]thian-4-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295438/ https://www.ncbi.nlm.nih.gov/pubmed/22412549 http://dx.doi.org/10.1107/S1600536812004680 |
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