(2E)-1-(5-Chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one

In the title mol­ecule, C(16)H(15)ClO(4)S, the chloro­thio­phene and trimeth­oxy­phenyl rings make a dihedral angle of 31.12 (5)°. The C=C double bond exhibits an E conformation. In the crystal, C—H⋯O inter­actions generate bifurcated bonds, linking the mol­ecules into chains along the b axis....

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Detalles Bibliográficos
Autores principales: Prabhu, A. N., Jayarama, A., Row, T. N. Guru, Upadhyaya, V.
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/PMC3213527/
https://www.ncbi.nlm.nih.gov/pubmed/22091106
http://dx.doi.org/10.1107/S1600536811028236
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author Prabhu, A. N.
Jayarama, A.
Row, T. N. Guru
Upadhyaya, V.
author_facet Prabhu, A. N.
Jayarama, A.
Row, T. N. Guru
Upadhyaya, V.
author_sort Prabhu, A. N.
collection PubMed
description In the title mol­ecule, C(16)H(15)ClO(4)S, the chloro­thio­phene and trimeth­oxy­phenyl rings make a dihedral angle of 31.12 (5)°. The C=C double bond exhibits an E conformation. In the crystal, C—H⋯O inter­actions generate bifurcated bonds, linking the mol­ecules into chains along the b axis.
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spelling pubmed-32135272011-11-16 (2E)-1-(5-Chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one Prabhu, A. N. Jayarama, A. Row, T. N. Guru Upadhyaya, V. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(16)H(15)ClO(4)S, the chloro­thio­phene and trimeth­oxy­phenyl rings make a dihedral angle of 31.12 (5)°. The C=C double bond exhibits an E conformation. In the crystal, C—H⋯O inter­actions generate bifurcated bonds, linking the mol­ecules into chains along the b axis. International Union of Crystallography 2011-07-23 /pmc/articles/PMC3213527/ /pubmed/22091106 http://dx.doi.org/10.1107/S1600536811028236 Text en © Prabhu 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
Prabhu, A. N.
Jayarama, A.
Row, T. N. Guru
Upadhyaya, V.
(2E)-1-(5-Chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title (2E)-1-(5-Chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_full (2E)-1-(5-Chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_fullStr (2E)-1-(5-Chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_full_unstemmed (2E)-1-(5-Chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_short (2E)-1-(5-Chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_sort (2e)-1-(5-chloro­thio­phen-2-yl)-3-(2,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213527/
https://www.ncbi.nlm.nih.gov/pubmed/22091106
http://dx.doi.org/10.1107/S1600536811028236
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