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3-(4-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran
In the title molecule, C(17)H(15)FO(2)S, the O atom and the 4-fluorophenyl group of the 4-fluorophenylsulfinyl substituent lie on opposite sides of the benzofuran fragment. The mean planes of the benzofuran and 4-fluorophenyl fragments form a dihedral angle of 86.07 (4)°. In the crystal structu...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979946/ https://www.ncbi.nlm.nih.gov/pubmed/21579882 http://dx.doi.org/10.1107/S160053681000293X |
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author | Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk |
author_facet | Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk |
author_sort | Choi, Hong Dae |
collection | PubMed |
description | In the title molecule, C(17)H(15)FO(2)S, the O atom and the 4-fluorophenyl group of the 4-fluorophenylsulfinyl substituent lie on opposite sides of the benzofuran fragment. The mean planes of the benzofuran and 4-fluorophenyl fragments form a dihedral angle of 86.07 (4)°. In the crystal structure, weak intermolecular C—H⋯O hydrogen bonds link the molecules into centrosymmetric dimers, which are further linked via intermolecular C—H⋯π interactions. |
format | Text |
id | pubmed-2979946 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29799462010-12-30 3-(4-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title molecule, C(17)H(15)FO(2)S, the O atom and the 4-fluorophenyl group of the 4-fluorophenylsulfinyl substituent lie on opposite sides of the benzofuran fragment. The mean planes of the benzofuran and 4-fluorophenyl fragments form a dihedral angle of 86.07 (4)°. In the crystal structure, weak intermolecular C—H⋯O hydrogen bonds link the molecules into centrosymmetric dimers, which are further linked via intermolecular C—H⋯π interactions. International Union of Crystallography 2010-01-30 /pmc/articles/PMC2979946/ /pubmed/21579882 http://dx.doi.org/10.1107/S160053681000293X Text en © Choi 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 Choi, Hong Dae Seo, Pil Ja Son, Byeng Wha Lee, Uk 3-(4-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran |
title | 3-(4-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran |
title_full | 3-(4-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran |
title_fullStr | 3-(4-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran |
title_full_unstemmed | 3-(4-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran |
title_short | 3-(4-Fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran |
title_sort | 3-(4-fluorophenylsulfinyl)-2,5,7-trimethyl-1-benzofuran |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979946/ https://www.ncbi.nlm.nih.gov/pubmed/21579882 http://dx.doi.org/10.1107/S160053681000293X |
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