(5Z)-5-(2-Hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one

In the title compound, C(17)H(13)NO(2)S(2), the dihedral angles between the 2-sulfanyl­idene-1,3-thia­zolidin-4-one group and the pendant toluene and 2-hy­droxy­benzene rings are 74.62 (6) and 8.73 (12)°, respectively. An intra­molecular C—H⋯S inter­action occurs. In the crystal, inversion dimers li...

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Autores principales: Shahwar, Durre, Tahir, M. Nawaz, Kashif, Misbah, Saeed, Afifa, Bukhari, Sana
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/PMC3379392/
https://www.ncbi.nlm.nih.gov/pubmed/22719590
http://dx.doi.org/10.1107/S1600536812021630
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author Shahwar, Durre
Tahir, M. Nawaz
Kashif, Misbah
Saeed, Afifa
Bukhari, Sana
author_facet Shahwar, Durre
Tahir, M. Nawaz
Kashif, Misbah
Saeed, Afifa
Bukhari, Sana
author_sort Shahwar, Durre
collection PubMed
description In the title compound, C(17)H(13)NO(2)S(2), the dihedral angles between the 2-sulfanyl­idene-1,3-thia­zolidin-4-one group and the pendant toluene and 2-hy­droxy­benzene rings are 74.62 (6) and 8.73 (12)°, respectively. An intra­molecular C—H⋯S inter­action occurs. In the crystal, inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R (2) (2)(16) loops. This link is reinforced by a pair of C—H⋯O hydrogen bonds. The dimers are connected by weak C—H⋯S inter­actions.
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spelling pubmed-33793922012-06-20 (5Z)-5-(2-Hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one Shahwar, Durre Tahir, M. Nawaz Kashif, Misbah Saeed, Afifa Bukhari, Sana Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(13)NO(2)S(2), the dihedral angles between the 2-sulfanyl­idene-1,3-thia­zolidin-4-one group and the pendant toluene and 2-hy­droxy­benzene rings are 74.62 (6) and 8.73 (12)°, respectively. An intra­molecular C—H⋯S inter­action occurs. In the crystal, inversion dimers linked by pairs of O—H⋯O hydrogen bonds generate R (2) (2)(16) loops. This link is reinforced by a pair of C—H⋯O hydrogen bonds. The dimers are connected by weak C—H⋯S inter­actions. International Union of Crystallography 2012-05-19 /pmc/articles/PMC3379392/ /pubmed/22719590 http://dx.doi.org/10.1107/S1600536812021630 Text en © Shahwar 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
Shahwar, Durre
Tahir, M. Nawaz
Kashif, Misbah
Saeed, Afifa
Bukhari, Sana
(5Z)-5-(2-Hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title (5Z)-5-(2-Hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_full (5Z)-5-(2-Hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_fullStr (5Z)-5-(2-Hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_full_unstemmed (5Z)-5-(2-Hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_short (5Z)-5-(2-Hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_sort (5z)-5-(2-hy­droxy­benzyl­idene)-3-(4-methyl­phen­yl)-2-sulfanyl­idene-1,3-thia­zolidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379392/
https://www.ncbi.nlm.nih.gov/pubmed/22719590
http://dx.doi.org/10.1107/S1600536812021630
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