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1-(2-Nitrophenyl)-3-phenylthiourea
The title compound, C(13)H(11)N(3)O(2)S, was prepared by reaction of 2-nitrobenzenamine, KOH and 1-isothiocyanatobenzene in an ethanol solution at room temperature. The dihedral angles formed between the thiourea plane and the phenyl rings are 61.9 and 31.0°. The dihedral angle between the two ph...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915211/ https://www.ncbi.nlm.nih.gov/pubmed/21200707 http://dx.doi.org/10.1107/S1600536807063374 |
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author | Qin, Yongqi Jian, Fangfang Jiang, Mingna Yang, Xiangyan |
author_facet | Qin, Yongqi Jian, Fangfang Jiang, Mingna Yang, Xiangyan |
author_sort | Qin, Yongqi |
collection | PubMed |
description | The title compound, C(13)H(11)N(3)O(2)S, was prepared by reaction of 2-nitrobenzenamine, KOH and 1-isothiocyanatobenzene in an ethanol solution at room temperature. The dihedral angles formed between the thiourea plane and the phenyl rings are 61.9 and 31.0°. The dihedral angle between the two phenyl rings is 78.1°. In the crystal structure, there are weak intermolecular N—H⋯S and C—H⋯S hydrogen-bonding interactions. |
format | Text |
id | pubmed-2915211 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29152112010-12-30 1-(2-Nitrophenyl)-3-phenylthiourea Qin, Yongqi Jian, Fangfang Jiang, Mingna Yang, Xiangyan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(11)N(3)O(2)S, was prepared by reaction of 2-nitrobenzenamine, KOH and 1-isothiocyanatobenzene in an ethanol solution at room temperature. The dihedral angles formed between the thiourea plane and the phenyl rings are 61.9 and 31.0°. The dihedral angle between the two phenyl rings is 78.1°. In the crystal structure, there are weak intermolecular N—H⋯S and C—H⋯S hydrogen-bonding interactions. International Union of Crystallography 2007-12-06 /pmc/articles/PMC2915211/ /pubmed/21200707 http://dx.doi.org/10.1107/S1600536807063374 Text en © International Union of Crystallography 2008 http://journals.iucr.org/services/termsofuse.html This is an open-access article distributed under the terms described at http://journals.iucr.org/services/termsofuse.html. |
spellingShingle | Organic Papers Qin, Yongqi Jian, Fangfang Jiang, Mingna Yang, Xiangyan 1-(2-Nitrophenyl)-3-phenylthiourea |
title | 1-(2-Nitrophenyl)-3-phenylthiourea |
title_full | 1-(2-Nitrophenyl)-3-phenylthiourea |
title_fullStr | 1-(2-Nitrophenyl)-3-phenylthiourea |
title_full_unstemmed | 1-(2-Nitrophenyl)-3-phenylthiourea |
title_short | 1-(2-Nitrophenyl)-3-phenylthiourea |
title_sort | 1-(2-nitrophenyl)-3-phenylthiourea |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915211/ https://www.ncbi.nlm.nih.gov/pubmed/21200707 http://dx.doi.org/10.1107/S1600536807063374 |
work_keys_str_mv | AT qinyongqi 12nitrophenyl3phenylthiourea AT jianfangfang 12nitrophenyl3phenylthiourea AT jiangmingna 12nitrophenyl3phenylthiourea AT yangxiangyan 12nitrophenyl3phenylthiourea |