(E)-1-(4-Chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one

The asymmetric unit of the title chalcone derivative, C(19)H(20)ClNO, contains two independent mol­ecules, which differ in the conformations of the ethyl groups in the diethyl­amino substituents. In the crystal, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules into ribbons propogating in [0...

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Detalles Bibliográficos
Autores principales: Kobkeatthawin, Thawanrat, Chantrapromma, Suchada, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979838/
https://www.ncbi.nlm.nih.gov/pubmed/21579698
http://dx.doi.org/10.1107/S1600536809054683
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author Kobkeatthawin, Thawanrat
Chantrapromma, Suchada
Fun, Hoong-Kun
author_facet Kobkeatthawin, Thawanrat
Chantrapromma, Suchada
Fun, Hoong-Kun
author_sort Kobkeatthawin, Thawanrat
collection PubMed
description The asymmetric unit of the title chalcone derivative, C(19)H(20)ClNO, contains two independent mol­ecules, which differ in the conformations of the ethyl groups in the diethyl­amino substituents. In the crystal, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules into ribbons propogating in [010]. The crystal packing also exhibits weak C—H⋯π inter­actions.
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spelling pubmed-29798382010-12-30 (E)-1-(4-Chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one Kobkeatthawin, Thawanrat Chantrapromma, Suchada Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title chalcone derivative, C(19)H(20)ClNO, contains two independent mol­ecules, which differ in the conformations of the ethyl groups in the diethyl­amino substituents. In the crystal, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules into ribbons propogating in [010]. The crystal packing also exhibits weak C—H⋯π inter­actions. International Union of Crystallography 2010-01-09 /pmc/articles/PMC2979838/ /pubmed/21579698 http://dx.doi.org/10.1107/S1600536809054683 Text en © Kobkeatthawin et al. 2010 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
Kobkeatthawin, Thawanrat
Chantrapromma, Suchada
Fun, Hoong-Kun
(E)-1-(4-Chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one
title (E)-1-(4-Chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one
title_full (E)-1-(4-Chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one
title_fullStr (E)-1-(4-Chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one
title_full_unstemmed (E)-1-(4-Chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one
title_short (E)-1-(4-Chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one
title_sort (e)-1-(4-chloro­phen­yl)-3-[4-(diethyl­amino)phen­yl]prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979838/
https://www.ncbi.nlm.nih.gov/pubmed/21579698
http://dx.doi.org/10.1107/S1600536809054683
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AT funhoongkun e14chlorophenyl34diethylaminophenylprop2en1one

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