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6-Chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole
The title compound, C(16)H(11)ClN(2)S(2), co-crystallizes with a small amount of the 5-chloro- isomer. The ratio of 6-chloro- to 5-chloro- isomers is 0.969 (2):0.031 (2). One thiophen-2-yl substitutent displays rotational disorder with 80.6 (4)% of the molecules exhibiting the major orientation. I...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648326/ https://www.ncbi.nlm.nih.gov/pubmed/23723946 http://dx.doi.org/10.1107/S1600536813011124 |
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author | Geiger, David K. Nellist, Michael R. |
author_facet | Geiger, David K. Nellist, Michael R. |
author_sort | Geiger, David K. |
collection | PubMed |
description | The title compound, C(16)H(11)ClN(2)S(2), co-crystallizes with a small amount of the 5-chloro- isomer. The ratio of 6-chloro- to 5-chloro- isomers is 0.969 (2):0.031 (2). One thiophen-2-yl substitutent displays rotational disorder with 80.6 (4)% of the molecules exhibiting the major orientation. In the crystal, weak C—H⋯N and C—H⋯S hydrogen-bonding interactions result in chains of molecules parallel to [001]. |
format | Online Article Text |
id | pubmed-3648326 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-36483262013-05-30 6-Chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole Geiger, David K. Nellist, Michael R. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(11)ClN(2)S(2), co-crystallizes with a small amount of the 5-chloro- isomer. The ratio of 6-chloro- to 5-chloro- isomers is 0.969 (2):0.031 (2). One thiophen-2-yl substitutent displays rotational disorder with 80.6 (4)% of the molecules exhibiting the major orientation. In the crystal, weak C—H⋯N and C—H⋯S hydrogen-bonding interactions result in chains of molecules parallel to [001]. International Union of Crystallography 2013-04-30 /pmc/articles/PMC3648326/ /pubmed/23723946 http://dx.doi.org/10.1107/S1600536813011124 Text en © Geiger and Nellist 2013 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 Geiger, David K. Nellist, Michael R. 6-Chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole |
title | 6-Chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole |
title_full | 6-Chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole |
title_fullStr | 6-Chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole |
title_full_unstemmed | 6-Chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole |
title_short | 6-Chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole |
title_sort | 6-chloro-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1h-benzimidazole |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648326/ https://www.ncbi.nlm.nih.gov/pubmed/23723946 http://dx.doi.org/10.1107/S1600536813011124 |
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