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2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone
The naphthoquinone ring is almost perpendicular [dihedral angle 71.02 (3)°] to the phenyl group of the title compound, C(17)H(9)Cl(2)NO(3), while the dihedral angle between the amide group and the 4-chlorophenyl ring is 21.9 (2)°. The conformation of the N—H and C=O bonds are anti to each other. N—...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967976/ https://www.ncbi.nlm.nih.gov/pubmed/21581704 http://dx.doi.org/10.1107/S1600536808040993 |
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author | Brandy, Yakini Butcher, Ray J. Adesiyun, Tolulope A. Berhe, Solomon Bakare, Oladapo |
author_facet | Brandy, Yakini Butcher, Ray J. Adesiyun, Tolulope A. Berhe, Solomon Bakare, Oladapo |
author_sort | Brandy, Yakini |
collection | PubMed |
description | The naphthoquinone ring is almost perpendicular [dihedral angle 71.02 (3)°] to the phenyl group of the title compound, C(17)H(9)Cl(2)NO(3), while the dihedral angle between the amide group and the 4-chlorophenyl ring is 21.9 (2)°. The conformation of the N—H and C=O bonds are anti to each other. N—H⋯Cl hydrogen bonds link the molecules into chains in the a-axis direction. In addition, these chains are linked by weak intermolecular C—H⋯O interactions. |
format | Text |
id | pubmed-2967976 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29679762010-12-30 2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone Brandy, Yakini Butcher, Ray J. Adesiyun, Tolulope A. Berhe, Solomon Bakare, Oladapo Acta Crystallogr Sect E Struct Rep Online Organic Papers The naphthoquinone ring is almost perpendicular [dihedral angle 71.02 (3)°] to the phenyl group of the title compound, C(17)H(9)Cl(2)NO(3), while the dihedral angle between the amide group and the 4-chlorophenyl ring is 21.9 (2)°. The conformation of the N—H and C=O bonds are anti to each other. N—H⋯Cl hydrogen bonds link the molecules into chains in the a-axis direction. In addition, these chains are linked by weak intermolecular C—H⋯O interactions. International Union of Crystallography 2008-12-10 /pmc/articles/PMC2967976/ /pubmed/21581704 http://dx.doi.org/10.1107/S1600536808040993 Text en © Brandy et al. 2009 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 Brandy, Yakini Butcher, Ray J. Adesiyun, Tolulope A. Berhe, Solomon Bakare, Oladapo 2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone |
title | 2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone |
title_full | 2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone |
title_fullStr | 2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone |
title_full_unstemmed | 2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone |
title_short | 2-Chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone |
title_sort | 2-chloro-3-(4-chlorobenzamido)-1,4-naphthoquinone |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2967976/ https://www.ncbi.nlm.nih.gov/pubmed/21581704 http://dx.doi.org/10.1107/S1600536808040993 |
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