5-Chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran

In the title compound, C(16)H(19)ClO(2)S, the cyclo­hexyl ring adopts a chair conformation and the aryl­sulfinyl unit is positioned equatorial relative to the cyclo­hexyl group. The least-squares plane through all six C atoms of the cyclo­hexyl ring makes a dihedral angle of 74.80 (6)° with the mean...

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Detalles Bibliográficos
Autores principales: Choi, Hong Dae, Seo, Pil Ja, Lee, Uk
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200660/
https://www.ncbi.nlm.nih.gov/pubmed/22058984
http://dx.doi.org/10.1107/S1600536811033095
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author Choi, Hong Dae
Seo, Pil Ja
Lee, Uk
author_facet Choi, Hong Dae
Seo, Pil Ja
Lee, Uk
author_sort Choi, Hong Dae
collection PubMed
description In the title compound, C(16)H(19)ClO(2)S, the cyclo­hexyl ring adopts a chair conformation and the aryl­sulfinyl unit is positioned equatorial relative to the cyclo­hexyl group. The least-squares plane through all six C atoms of the cyclo­hexyl ring makes a dihedral angle of 74.80 (6)° with the mean plane of the benzofuran fragment. In the crystal, mol­ecules are linked through inter­molecular C—H⋯O hydrogen bonds.
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spelling pubmed-32006602011-11-06 5-Chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran Choi, Hong Dae Seo, Pil Ja Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(16)H(19)ClO(2)S, the cyclo­hexyl ring adopts a chair conformation and the aryl­sulfinyl unit is positioned equatorial relative to the cyclo­hexyl group. The least-squares plane through all six C atoms of the cyclo­hexyl ring makes a dihedral angle of 74.80 (6)° with the mean plane of the benzofuran fragment. In the crystal, mol­ecules are linked through inter­molecular C—H⋯O hydrogen bonds. International Union of Crystallography 2011-08-27 /pmc/articles/PMC3200660/ /pubmed/22058984 http://dx.doi.org/10.1107/S1600536811033095 Text en © Choi 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
Choi, Hong Dae
Seo, Pil Ja
Lee, Uk
5-Chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran
title 5-Chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran
title_full 5-Chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran
title_fullStr 5-Chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran
title_full_unstemmed 5-Chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran
title_short 5-Chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran
title_sort 5-chloro-3-cyclo­hexyl­sulfinyl-2,7-dimethyl-1-benzofuran
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200660/
https://www.ncbi.nlm.nih.gov/pubmed/22058984
http://dx.doi.org/10.1107/S1600536811033095
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AT seopilja 5chloro3cyclohexylsulfinyl27dimethyl1benzofuran
AT leeuk 5chloro3cyclohexylsulfinyl27dimethyl1benzofuran

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