3-[(5-Chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one

In the title compound, C(10)H(7)ClN(2)O(2)S(2), the mean plane of the thioxo­thia­zolidine ring [maximum deviation = 0.032 (2) Å] is inclined to the benzene ring by 12.25 (4)°. There is a strong intra­molecular O—H⋯N hydrogen bond present. In the crystal, mol­ecules are linked via pairs of C—H⋯Cl hy...

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Detalles Bibliográficos
Autor principal: Dal, Hakan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770396/
https://www.ncbi.nlm.nih.gov/pubmed/24046681
http://dx.doi.org/10.1107/S1600536813016577
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author Dal, Hakan
author_facet Dal, Hakan
author_sort Dal, Hakan
collection PubMed
description In the title compound, C(10)H(7)ClN(2)O(2)S(2), the mean plane of the thioxo­thia­zolidine ring [maximum deviation = 0.032 (2) Å] is inclined to the benzene ring by 12.25 (4)°. There is a strong intra­molecular O—H⋯N hydrogen bond present. In the crystal, mol­ecules are linked via pairs of C—H⋯Cl hydrogen bonds, forming inversion dimers.
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spelling pubmed-37703962013-09-17 3-[(5-Chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one Dal, Hakan Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(7)ClN(2)O(2)S(2), the mean plane of the thioxo­thia­zolidine ring [maximum deviation = 0.032 (2) Å] is inclined to the benzene ring by 12.25 (4)°. There is a strong intra­molecular O—H⋯N hydrogen bond present. In the crystal, mol­ecules are linked via pairs of C—H⋯Cl hydrogen bonds, forming inversion dimers. International Union of Crystallography 2013-06-19 /pmc/articles/PMC3770396/ /pubmed/24046681 http://dx.doi.org/10.1107/S1600536813016577 Text en © Hakan Dal 2013 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
Dal, Hakan
3-[(5-Chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title 3-[(5-Chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_full 3-[(5-Chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_fullStr 3-[(5-Chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_full_unstemmed 3-[(5-Chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_short 3-[(5-Chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one
title_sort 3-[(5-chloro-2-hy­droxy­benzyl­idene)amino]-2-sulfanyl­idene-1,3-thia­zolidin-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3770396/
https://www.ncbi.nlm.nih.gov/pubmed/24046681
http://dx.doi.org/10.1107/S1600536813016577
work_keys_str_mv AT dalhakan 35chloro2hydroxybenzylideneamino2sulfanylidene13thiazolidin4one

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