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2-(4-Fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-1-benzofuran

In the title compound, C(16)H(11)FO(4)S, the O atom and the methyl group of the methyl­sulfinyl substituent are located on opposite sides of the mean plane through the 5,6-(methyl­enedi­oxy)benzofuran fragment. The 4-fluoro­phenyl ring is rotated out of the 5,6-(methyl­enedi­oxy)benzofuran plane, ma...

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Detalles Bibliográficos
Autores principales: Choi, Hong Dae, Seo, Pil Ja, Son, Byeng Wha, Lee, Uk
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983733/
https://www.ncbi.nlm.nih.gov/pubmed/21580364
http://dx.doi.org/10.1107/S1600536810004745
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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 compound, C(16)H(11)FO(4)S, the O atom and the methyl group of the methyl­sulfinyl substituent are located on opposite sides of the mean plane through the 5,6-(methyl­enedi­oxy)benzofuran fragment. The 4-fluoro­phenyl ring is rotated out of the 5,6-(methyl­enedi­oxy)benzofuran plane, making a dihedral angle of 29.90 (6)°. In the crystal structure, both inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers. The combination of C—H⋯O hydrogen bonds result in chains running along [1[Image: see text] [Image: see text]].
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spelling pubmed-29837332010-12-30 2-(4-Fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-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 compound, C(16)H(11)FO(4)S, the O atom and the methyl group of the methyl­sulfinyl substituent are located on opposite sides of the mean plane through the 5,6-(methyl­enedi­oxy)benzofuran fragment. The 4-fluoro­phenyl ring is rotated out of the 5,6-(methyl­enedi­oxy)benzofuran plane, making a dihedral angle of 29.90 (6)°. In the crystal structure, both inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers. The combination of C—H⋯O hydrogen bonds result in chains running along [1[Image: see text] [Image: see text]]. International Union of Crystallography 2010-02-13 /pmc/articles/PMC2983733/ /pubmed/21580364 http://dx.doi.org/10.1107/S1600536810004745 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
2-(4-Fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-1-benzofuran
title 2-(4-Fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-1-benzofuran
title_full 2-(4-Fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-1-benzofuran
title_fullStr 2-(4-Fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-1-benzofuran
title_full_unstemmed 2-(4-Fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-1-benzofuran
title_short 2-(4-Fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-1-benzofuran
title_sort 2-(4-fluoro­phen­yl)-5,6-methyl­enedi­oxy-3-methyl­sulfinyl-1-benzofuran
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983733/
https://www.ncbi.nlm.nih.gov/pubmed/21580364
http://dx.doi.org/10.1107/S1600536810004745
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