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5-(4-Bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine
The title compound, C(8)H(5)BrN(4)O(2)S, was synthesized by the reaction of 4-bromo-2-nitrobenzoic acid with thiosemicarbazide. The dihedral angle between the thiadiazole and benzene rings is 40.5 (2)°. In the crystal, the strongest N—H⋯N intermolecular hydrogen bond, between the amine group an...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200604/ https://www.ncbi.nlm.nih.gov/pubmed/22058914 http://dx.doi.org/10.1107/S1600536811030868 |
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author | Zhang, Jian-qiang He, Qiu Jiang, Qianghua Mu, Haipin Wan, Rong |
author_facet | Zhang, Jian-qiang He, Qiu Jiang, Qianghua Mu, Haipin Wan, Rong |
author_sort | Zhang, Jian-qiang |
collection | PubMed |
description | The title compound, C(8)H(5)BrN(4)O(2)S, was synthesized by the reaction of 4-bromo-2-nitrobenzoic acid with thiosemicarbazide. The dihedral angle between the thiadiazole and benzene rings is 40.5 (2)°. In the crystal, the strongest N—H⋯N intermolecular hydrogen bond, between the amine group and one thiadiazole N atom, forms centrosymmetric dimers. The other amine H atom extends the supramolecular network, forming an N—H⋯N contact with the other thiadiazole N atom. |
format | Online Article Text |
id | pubmed-3200604 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32006042011-11-06 5-(4-Bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine Zhang, Jian-qiang He, Qiu Jiang, Qianghua Mu, Haipin Wan, Rong Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(8)H(5)BrN(4)O(2)S, was synthesized by the reaction of 4-bromo-2-nitrobenzoic acid with thiosemicarbazide. The dihedral angle between the thiadiazole and benzene rings is 40.5 (2)°. In the crystal, the strongest N—H⋯N intermolecular hydrogen bond, between the amine group and one thiadiazole N atom, forms centrosymmetric dimers. The other amine H atom extends the supramolecular network, forming an N—H⋯N contact with the other thiadiazole N atom. International Union of Crystallography 2011-08-06 /pmc/articles/PMC3200604/ /pubmed/22058914 http://dx.doi.org/10.1107/S1600536811030868 Text en © Zhang et al. 2011 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 Zhang, Jian-qiang He, Qiu Jiang, Qianghua Mu, Haipin Wan, Rong 5-(4-Bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine |
title | 5-(4-Bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine |
title_full | 5-(4-Bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine |
title_fullStr | 5-(4-Bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine |
title_full_unstemmed | 5-(4-Bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine |
title_short | 5-(4-Bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine |
title_sort | 5-(4-bromo-2-nitrophenyl)-1,3,4-thiadiazol-2-amine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200604/ https://www.ncbi.nlm.nih.gov/pubmed/22058914 http://dx.doi.org/10.1107/S1600536811030868 |
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