(E)-3-(3-Bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one

The title compound, C(16)H(13)BrO, was synthesized from the reaction of 3-bromo­benzaldehyde and 4-methyl­acetophenone in the presence of KOH. The mol­ecule adopts an E configuration with respect to the C=C double bond of the propenone unit. The dihedral angle formed by the aromatic rings is 46.91 (...

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Detalles Bibliográficos
Autores principales: Li, Hongqi, Sarojini, B. K., Raj, C. G. D., Madhu, L. N., Yathirajan, H. S.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959749/
https://www.ncbi.nlm.nih.gov/pubmed/21581092
http://dx.doi.org/10.1107/S1600536808034867
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author Li, Hongqi
Sarojini, B. K.
Raj, C. G. D.
Madhu, L. N.
Yathirajan, H. S.
author_facet Li, Hongqi
Sarojini, B. K.
Raj, C. G. D.
Madhu, L. N.
Yathirajan, H. S.
author_sort Li, Hongqi
collection PubMed
description The title compound, C(16)H(13)BrO, was synthesized from the reaction of 3-bromo­benzaldehyde and 4-methyl­acetophenone in the presence of KOH. The mol­ecule adopts an E configuration with respect to the C=C double bond of the propenone unit. The dihedral angle formed by the aromatic rings is 46.91 (14)°. The crystal structure is stabilized by Br⋯Br inter­actions [3.4549 (11) Å].
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spelling pubmed-29597492010-12-30 (E)-3-(3-Bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one Li, Hongqi Sarojini, B. K. Raj, C. G. D. Madhu, L. N. Yathirajan, H. S. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(13)BrO, was synthesized from the reaction of 3-bromo­benzaldehyde and 4-methyl­acetophenone in the presence of KOH. The mol­ecule adopts an E configuration with respect to the C=C double bond of the propenone unit. The dihedral angle formed by the aromatic rings is 46.91 (14)°. The crystal structure is stabilized by Br⋯Br inter­actions [3.4549 (11) Å]. International Union of Crystallography 2008-10-31 /pmc/articles/PMC2959749/ /pubmed/21581092 http://dx.doi.org/10.1107/S1600536808034867 Text en © Li 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
Li, Hongqi
Sarojini, B. K.
Raj, C. G. D.
Madhu, L. N.
Yathirajan, H. S.
(E)-3-(3-Bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one
title (E)-3-(3-Bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one
title_full (E)-3-(3-Bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one
title_fullStr (E)-3-(3-Bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one
title_full_unstemmed (E)-3-(3-Bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one
title_short (E)-3-(3-Bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one
title_sort (e)-3-(3-bromo­phen­yl)-1-(4-methyl­phenyl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959749/
https://www.ncbi.nlm.nih.gov/pubmed/21581092
http://dx.doi.org/10.1107/S1600536808034867
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AT madhuln e33bromophenyl14methylphenylprop2en1one
AT yathirajanhs e33bromophenyl14methylphenylprop2en1one

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