(E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one

In the title mol­ecule, C(15)H(14)O(4), the benzene and furyl rings are inclined to each other with a dihedral angle of 41.5 (1)°. An intra­molecular C—H⋯O hydrogen-bond inter­action generates an S(5) ring motif. In the crystal structure, mol­ecules are stacked along the b axis and the crystal packi...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Patil, P. S., Jebas, Samuel Robinson, Dharmaprakash, S. M.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962066/
https://www.ncbi.nlm.nih.gov/pubmed/21203150
http://dx.doi.org/10.1107/S1600536808020539
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author Fun, Hoong-Kun
Patil, P. S.
Jebas, Samuel Robinson
Dharmaprakash, S. M.
author_facet Fun, Hoong-Kun
Patil, P. S.
Jebas, Samuel Robinson
Dharmaprakash, S. M.
author_sort Fun, Hoong-Kun
collection PubMed
description In the title mol­ecule, C(15)H(14)O(4), the benzene and furyl rings are inclined to each other with a dihedral angle of 41.5 (1)°. An intra­molecular C—H⋯O hydrogen-bond inter­action generates an S(5) ring motif. In the crystal structure, mol­ecules are stacked along the b axis and the crystal packing is stabilized by inter­molecular C—H⋯O and C—H⋯π inter­actions. In addition, π–π stacking inter­actions with a centroid-to-centroid distance of 3.5855 (11) Å are observed.
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spelling pubmed-29620662010-12-30 (E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one Fun, Hoong-Kun Patil, P. S. Jebas, Samuel Robinson Dharmaprakash, S. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(15)H(14)O(4), the benzene and furyl rings are inclined to each other with a dihedral angle of 41.5 (1)°. An intra­molecular C—H⋯O hydrogen-bond inter­action generates an S(5) ring motif. In the crystal structure, mol­ecules are stacked along the b axis and the crystal packing is stabilized by inter­molecular C—H⋯O and C—H⋯π inter­actions. In addition, π–π stacking inter­actions with a centroid-to-centroid distance of 3.5855 (11) Å are observed. International Union of Crystallography 2008-07-09 /pmc/articles/PMC2962066/ /pubmed/21203150 http://dx.doi.org/10.1107/S1600536808020539 Text en © Fun et al. 2008 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
Fun, Hoong-Kun
Patil, P. S.
Jebas, Samuel Robinson
Dharmaprakash, S. M.
(E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one
title (E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one
title_full (E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one
title_fullStr (E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one
title_full_unstemmed (E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one
title_short (E)-3-(3,4-Dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one
title_sort (e)-3-(3,4-dimethoxy­phen­yl)-1-(2-fur­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962066/
https://www.ncbi.nlm.nih.gov/pubmed/21203150
http://dx.doi.org/10.1107/S1600536808020539
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