2-(5-Cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid

In the title compound, C(19)H(24)O(3)S, the cylohexyl ring adopts a chair conformation. In the crystal, molecules are linked via pairs of O—H⋯O hydrogen bonds, forming inversion dimers. These dimers are further stabilized by weak inter­molecular C—H⋯π inter­actions, and by slipped π–π inter­actions...

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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 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275074/
https://www.ncbi.nlm.nih.gov/pubmed/22347019
http://dx.doi.org/10.1107/S1600536811055152
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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(19)H(24)O(3)S, the cylohexyl ring adopts a chair conformation. In the crystal, molecules are linked via pairs of O—H⋯O hydrogen bonds, forming inversion dimers. These dimers are further stabilized by weak inter­molecular C—H⋯π inter­actions, and by slipped π–π inter­actions between the furan rings of adjacent mol­ecules [centroid–centroid distance = 3.557 (2) Å, inter­planar distance = 3.301 (2) Å and slippage = 1.325 (2) Å].
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spelling pubmed-32750742012-02-15 2-(5-Cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid Choi, Hong Dae Seo, Pil Ja Lee, Uk Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(19)H(24)O(3)S, the cylohexyl ring adopts a chair conformation. In the crystal, molecules are linked via pairs of O—H⋯O hydrogen bonds, forming inversion dimers. These dimers are further stabilized by weak inter­molecular C—H⋯π inter­actions, and by slipped π–π inter­actions between the furan rings of adjacent mol­ecules [centroid–centroid distance = 3.557 (2) Å, inter­planar distance = 3.301 (2) Å and slippage = 1.325 (2) Å]. International Union of Crystallography 2012-01-14 /pmc/articles/PMC3275074/ /pubmed/22347019 http://dx.doi.org/10.1107/S1600536811055152 Text en © Choi et al. 2012 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
2-(5-Cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title 2-(5-Cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_full 2-(5-Cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_fullStr 2-(5-Cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_full_unstemmed 2-(5-Cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_short 2-(5-Cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid
title_sort 2-(5-cyclo­hexyl-3-isopropyl­sulfanyl-1-benzofuran-2-yl)acetic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3275074/
https://www.ncbi.nlm.nih.gov/pubmed/22347019
http://dx.doi.org/10.1107/S1600536811055152
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AT seopilja 25cyclohexyl3isopropylsulfanyl1benzofuran2ylaceticacid
AT leeuk 25cyclohexyl3isopropylsulfanyl1benzofuran2ylaceticacid

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