Cargando…

(2E,4E)-1-(2-Hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one

In the structure of the title chalcone, C(17)H(14)O(2), derived from cinnamaldehyde, the olefine group has a trans configuration. The mol­ecular conformation is stabilized by an intra­molecular O—H⋯O hydrogen-bond inter­action with graph-set motif S(6).

Detalles Bibliográficos
Autores principales: Silva, W. A., Gatto, C. C., Oliveira, G. R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200610/
https://www.ncbi.nlm.nih.gov/pubmed/22058899
http://dx.doi.org/10.1107/S160053681103025X
_version_ 1782214709419704320
author Silva, W. A.
Gatto, C. C.
Oliveira, G. R.
author_facet Silva, W. A.
Gatto, C. C.
Oliveira, G. R.
author_sort Silva, W. A.
collection PubMed
description In the structure of the title chalcone, C(17)H(14)O(2), derived from cinnamaldehyde, the olefine group has a trans configuration. The mol­ecular conformation is stabilized by an intra­molecular O—H⋯O hydrogen-bond inter­action with graph-set motif S(6).
format Online
Article
Text
id pubmed-3200610
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-32006102011-11-06 (2E,4E)-1-(2-Hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one Silva, W. A. Gatto, C. C. Oliveira, G. R. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the structure of the title chalcone, C(17)H(14)O(2), derived from cinnamaldehyde, the olefine group has a trans configuration. The mol­ecular conformation is stabilized by an intra­molecular O—H⋯O hydrogen-bond inter­action with graph-set motif S(6). International Union of Crystallography 2011-08-02 /pmc/articles/PMC3200610/ /pubmed/22058899 http://dx.doi.org/10.1107/S160053681103025X Text en © Silva 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
Silva, W. A.
Gatto, C. C.
Oliveira, G. R.
(2E,4E)-1-(2-Hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one
title (2E,4E)-1-(2-Hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one
title_full (2E,4E)-1-(2-Hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one
title_fullStr (2E,4E)-1-(2-Hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one
title_full_unstemmed (2E,4E)-1-(2-Hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one
title_short (2E,4E)-1-(2-Hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one
title_sort (2e,4e)-1-(2-hy­droxy­phen­yl)-5-phenyl­penta-2,4-dien-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200610/
https://www.ncbi.nlm.nih.gov/pubmed/22058899
http://dx.doi.org/10.1107/S160053681103025X
work_keys_str_mv AT silvawa 2e4e12hydroxyphenyl5phenylpenta24dien1one
AT gattocc 2e4e12hydroxyphenyl5phenylpenta24dien1one
AT oliveiragr 2e4e12hydroxyphenyl5phenylpenta24dien1one