2,6-Dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate

Mol­ecules of the title compound, C(16)H(10)Br(2)O(3), adopt an E conformation about the C=C double bond. The dihedral angle between the two aromatic rings is 78.0 (7)°. In the crystal, mol­ecules are linked through weak C—H⋯O hydrogen bonds.

Detalles Bibliográficos
Autores principales: Suresh Kumar, C., Jagadeesan, G., Dhamodaran, S., Ananth, Karthik, Aravindhan, S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470228/
https://www.ncbi.nlm.nih.gov/pubmed/23125672
http://dx.doi.org/10.1107/S1600536812037427
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author Suresh Kumar, C.
Jagadeesan, G.
Dhamodaran, S.
Ananth, Karthik
Aravindhan, S.
author_facet Suresh Kumar, C.
Jagadeesan, G.
Dhamodaran, S.
Ananth, Karthik
Aravindhan, S.
author_sort Suresh Kumar, C.
collection PubMed
description Mol­ecules of the title compound, C(16)H(10)Br(2)O(3), adopt an E conformation about the C=C double bond. The dihedral angle between the two aromatic rings is 78.0 (7)°. In the crystal, mol­ecules are linked through weak C—H⋯O hydrogen bonds.
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spelling pubmed-34702282012-11-02 2,6-Dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate Suresh Kumar, C. Jagadeesan, G. Dhamodaran, S. Ananth, Karthik Aravindhan, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers Mol­ecules of the title compound, C(16)H(10)Br(2)O(3), adopt an E conformation about the C=C double bond. The dihedral angle between the two aromatic rings is 78.0 (7)°. In the crystal, mol­ecules are linked through weak C—H⋯O hydrogen bonds. International Union of Crystallography 2012-09-08 /pmc/articles/PMC3470228/ /pubmed/23125672 http://dx.doi.org/10.1107/S1600536812037427 Text en © Suresh Kumar et al. 2012 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
Suresh Kumar, C.
Jagadeesan, G.
Dhamodaran, S.
Ananth, Karthik
Aravindhan, S.
2,6-Dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate
title 2,6-Dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate
title_full 2,6-Dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate
title_fullStr 2,6-Dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate
title_full_unstemmed 2,6-Dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate
title_short 2,6-Dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate
title_sort 2,6-dibromo-4-formyl­phenyl 3-phenyl­prop-2-enoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470228/
https://www.ncbi.nlm.nih.gov/pubmed/23125672
http://dx.doi.org/10.1107/S1600536812037427
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