(2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one

In the title compound, C(13)H(8)BrClOS, the thio­phene and phenyl rings are inclined by 40.69 (11)° to each other. The crystal structure is characterized by C—H⋯π inter­actions, which link the mol­ecules into broad layers parallel to (100). Short Br⋯Cl contacts [3.698 (1) Å] link these layers along...

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Autores principales: Kavitha, H. D., Roopashree, K. R., Vepuri, Suresh B., Devarajegowda, H. C., Devaru, Venkatesh B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684940/
https://www.ncbi.nlm.nih.gov/pubmed/23795042
http://dx.doi.org/10.1107/S1600536813012063
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author Kavitha, H. D.
Roopashree, K. R.
Vepuri, Suresh B.
Devarajegowda, H. C.
Devaru, Venkatesh B.
author_facet Kavitha, H. D.
Roopashree, K. R.
Vepuri, Suresh B.
Devarajegowda, H. C.
Devaru, Venkatesh B.
author_sort Kavitha, H. D.
collection PubMed
description In the title compound, C(13)H(8)BrClOS, the thio­phene and phenyl rings are inclined by 40.69 (11)° to each other. The crystal structure is characterized by C—H⋯π inter­actions, which link the mol­ecules into broad layers parallel to (100). Short Br⋯Cl contacts [3.698 (1) Å] link these layers along [100].
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spelling pubmed-36849402013-06-21 (2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one Kavitha, H. D. Roopashree, K. R. Vepuri, Suresh B. Devarajegowda, H. C. Devaru, Venkatesh B. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(8)BrClOS, the thio­phene and phenyl rings are inclined by 40.69 (11)° to each other. The crystal structure is characterized by C—H⋯π inter­actions, which link the mol­ecules into broad layers parallel to (100). Short Br⋯Cl contacts [3.698 (1) Å] link these layers along [100]. International Union of Crystallography 2013-05-11 /pmc/articles/PMC3684940/ /pubmed/23795042 http://dx.doi.org/10.1107/S1600536813012063 Text en © Kavitha et al. 2013 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
Kavitha, H. D.
Roopashree, K. R.
Vepuri, Suresh B.
Devarajegowda, H. C.
Devaru, Venkatesh B.
(2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one
title (2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one
title_full (2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one
title_fullStr (2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one
title_full_unstemmed (2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one
title_short (2E)-1-(5-Bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one
title_sort (2e)-1-(5-bromothiophen-2-yl)-3-(4-chloro­phen­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3684940/
https://www.ncbi.nlm.nih.gov/pubmed/23795042
http://dx.doi.org/10.1107/S1600536813012063
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