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2-[2-(Methylsulfanyl)benzimidazol-1-yl]ethanol
In the title compound, C(10)H(12)N(2)OS, the asymmetric unit consists of two independent molecules. In the crystal structure, molecules form R (4) (4)(28) centrosymmetric tetramers via O—H⋯N hydrogen bonds. These tetramers are stacked along the c axis via C—H⋯O hydrogen bonds. C—H⋯π and π–π inte...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979779/ https://www.ncbi.nlm.nih.gov/pubmed/21579857 http://dx.doi.org/10.1107/S1600536810001960 |
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author | Akonan, Ludovic Molou, Kouassi Yves Guillaume Adohi-Krou, Adjo Abou, Akoun Tenon, Abodou Jules |
author_facet | Akonan, Ludovic Molou, Kouassi Yves Guillaume Adohi-Krou, Adjo Abou, Akoun Tenon, Abodou Jules |
author_sort | Akonan, Ludovic |
collection | PubMed |
description | In the title compound, C(10)H(12)N(2)OS, the asymmetric unit consists of two independent molecules. In the crystal structure, molecules form R (4) (4)(28) centrosymmetric tetramers via O—H⋯N hydrogen bonds. These tetramers are stacked along the c axis via C—H⋯O hydrogen bonds. C—H⋯π and π–π interactions are also present; in the latter, the centroid–centroid distances are 4.075 (1) and 3.719 (1) Å. |
format | Text |
id | pubmed-2979779 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29797792010-12-30 2-[2-(Methylsulfanyl)benzimidazol-1-yl]ethanol Akonan, Ludovic Molou, Kouassi Yves Guillaume Adohi-Krou, Adjo Abou, Akoun Tenon, Abodou Jules Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(12)N(2)OS, the asymmetric unit consists of two independent molecules. In the crystal structure, molecules form R (4) (4)(28) centrosymmetric tetramers via O—H⋯N hydrogen bonds. These tetramers are stacked along the c axis via C—H⋯O hydrogen bonds. C—H⋯π and π–π interactions are also present; in the latter, the centroid–centroid distances are 4.075 (1) and 3.719 (1) Å. International Union of Crystallography 2010-01-23 /pmc/articles/PMC2979779/ /pubmed/21579857 http://dx.doi.org/10.1107/S1600536810001960 Text en © Akonan et al. 2010 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 Akonan, Ludovic Molou, Kouassi Yves Guillaume Adohi-Krou, Adjo Abou, Akoun Tenon, Abodou Jules 2-[2-(Methylsulfanyl)benzimidazol-1-yl]ethanol |
title | 2-[2-(Methylsulfanyl)benzimidazol-1-yl]ethanol |
title_full | 2-[2-(Methylsulfanyl)benzimidazol-1-yl]ethanol |
title_fullStr | 2-[2-(Methylsulfanyl)benzimidazol-1-yl]ethanol |
title_full_unstemmed | 2-[2-(Methylsulfanyl)benzimidazol-1-yl]ethanol |
title_short | 2-[2-(Methylsulfanyl)benzimidazol-1-yl]ethanol |
title_sort | 2-[2-(methylsulfanyl)benzimidazol-1-yl]ethanol |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979779/ https://www.ncbi.nlm.nih.gov/pubmed/21579857 http://dx.doi.org/10.1107/S1600536810001960 |
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