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(E)-3-(4-Chloro­phen­yl)-2-phenyl­prop-2-enoic acid

In the title mol­ecule, C(15)H(11)ClO(2), the mean planes of the benzene and phenyl rings are inclined at 69.06 (11)° with respect to each other. The crystal structure is stablized by strong inter­molecular O—H⋯O hydrogen bonds between the acid groups of pairs of mol­ecules related by inversion cent...

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Detalles Bibliográficos
Autores principales: Sadiq-ur-Rehman, Ali, Saqib, Shahzadi, Saira, Parvez, Masood
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969502/
https://www.ncbi.nlm.nih.gov/pubmed/21582844
http://dx.doi.org/10.1107/S1600536809021904
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author Sadiq-ur-Rehman,
Ali, Saqib
Shahzadi, Saira
Parvez, Masood
author_facet Sadiq-ur-Rehman,
Ali, Saqib
Shahzadi, Saira
Parvez, Masood
author_sort Sadiq-ur-Rehman,
collection PubMed
description In the title mol­ecule, C(15)H(11)ClO(2), the mean planes of the benzene and phenyl rings are inclined at 69.06 (11)° with respect to each other. The crystal structure is stablized by strong inter­molecular O—H⋯O hydrogen bonds between the acid groups of pairs of mol­ecules related by inversion centers.
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spelling pubmed-29695022010-12-30 (E)-3-(4-Chloro­phen­yl)-2-phenyl­prop-2-enoic acid Sadiq-ur-Rehman, Ali, Saqib Shahzadi, Saira Parvez, Masood Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(15)H(11)ClO(2), the mean planes of the benzene and phenyl rings are inclined at 69.06 (11)° with respect to each other. The crystal structure is stablized by strong inter­molecular O—H⋯O hydrogen bonds between the acid groups of pairs of mol­ecules related by inversion centers. International Union of Crystallography 2009-06-13 /pmc/articles/PMC2969502/ /pubmed/21582844 http://dx.doi.org/10.1107/S1600536809021904 Text en © Sadiq-ur-Rehman et al. 2009 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
Sadiq-ur-Rehman,
Ali, Saqib
Shahzadi, Saira
Parvez, Masood
(E)-3-(4-Chloro­phen­yl)-2-phenyl­prop-2-enoic acid
title (E)-3-(4-Chloro­phen­yl)-2-phenyl­prop-2-enoic acid
title_full (E)-3-(4-Chloro­phen­yl)-2-phenyl­prop-2-enoic acid
title_fullStr (E)-3-(4-Chloro­phen­yl)-2-phenyl­prop-2-enoic acid
title_full_unstemmed (E)-3-(4-Chloro­phen­yl)-2-phenyl­prop-2-enoic acid
title_short (E)-3-(4-Chloro­phen­yl)-2-phenyl­prop-2-enoic acid
title_sort (e)-3-(4-chloro­phen­yl)-2-phenyl­prop-2-enoic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969502/
https://www.ncbi.nlm.nih.gov/pubmed/21582844
http://dx.doi.org/10.1107/S1600536809021904
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