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

The title compound, C(19)H(20)O(5), was synthesized by reaction of 4-meth­oxy­acetophenone and 3,4,5-trimeth­oxy-benzaldehyde. The aromatic rings form a dihedral angle of 36.39 (7)°. Two intramolecular C—H⋯O hydrogen bonds occur. The crystal packing features weak C—H⋯O inter­actions.

Detalles Bibliográficos
Autores principales: Carvalho-Jr, P. S., Sallum, L. O., Cidade, A. F., Aquino, G. L. B., Napolitano, H. B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213567/
https://www.ncbi.nlm.nih.gov/pubmed/22091144
http://dx.doi.org/10.1107/S1600536811028984
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author Carvalho-Jr, P. S.
Sallum, L. O.
Cidade, A. F.
Aquino, G. L. B.
Napolitano, H. B.
author_facet Carvalho-Jr, P. S.
Sallum, L. O.
Cidade, A. F.
Aquino, G. L. B.
Napolitano, H. B.
author_sort Carvalho-Jr, P. S.
collection PubMed
description The title compound, C(19)H(20)O(5), was synthesized by reaction of 4-meth­oxy­acetophenone and 3,4,5-trimeth­oxy-benzaldehyde. The aromatic rings form a dihedral angle of 36.39 (7)°. Two intramolecular C—H⋯O hydrogen bonds occur. The crystal packing features weak C—H⋯O inter­actions.
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spelling pubmed-32135672011-11-16 (E)-1-(4-Meth­oxy­phen­yl)-3-(3,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one Carvalho-Jr, P. S. Sallum, L. O. Cidade, A. F. Aquino, G. L. B. Napolitano, H. B. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(19)H(20)O(5), was synthesized by reaction of 4-meth­oxy­acetophenone and 3,4,5-trimeth­oxy-benzaldehyde. The aromatic rings form a dihedral angle of 36.39 (7)°. Two intramolecular C—H⋯O hydrogen bonds occur. The crystal packing features weak C—H⋯O inter­actions. International Union of Crystallography 2011-07-23 /pmc/articles/PMC3213567/ /pubmed/22091144 http://dx.doi.org/10.1107/S1600536811028984 Text en © Carvalho-Jr 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
Carvalho-Jr, P. S.
Sallum, L. O.
Cidade, A. F.
Aquino, G. L. B.
Napolitano, H. B.
(E)-1-(4-Meth­oxy­phen­yl)-3-(3,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title (E)-1-(4-Meth­oxy­phen­yl)-3-(3,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_full (E)-1-(4-Meth­oxy­phen­yl)-3-(3,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_fullStr (E)-1-(4-Meth­oxy­phen­yl)-3-(3,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_full_unstemmed (E)-1-(4-Meth­oxy­phen­yl)-3-(3,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_short (E)-1-(4-Meth­oxy­phen­yl)-3-(3,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
title_sort (e)-1-(4-meth­oxy­phen­yl)-3-(3,4,5-trimeth­oxy­phen­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213567/
https://www.ncbi.nlm.nih.gov/pubmed/22091144
http://dx.doi.org/10.1107/S1600536811028984
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