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(E)-3-(2-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one
The title compound, C(13)H(9)ClO(2), adopts an E configuration with respect to the C=C double bond of the propenone unit. The benzene and furyl rings are twisted slightly from each other, making a dihedral angle of 6.47 (7)°. Intramolecular C—H⋯O and C—H⋯Cl hydrogen bonds generate an S(5)S(5)S(5) r...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962097/ https://www.ncbi.nlm.nih.gov/pubmed/21203181 http://dx.doi.org/10.1107/S1600536808020965 |
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author | Fun, Hoong-Kun Patil, P. S. Jebas, Samuel Robinson Dharmaprakash, S. M. |
author_facet | Fun, Hoong-Kun Patil, P. S. Jebas, Samuel Robinson Dharmaprakash, S. M. |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | The title compound, C(13)H(9)ClO(2), adopts an E configuration with respect to the C=C double bond of the propenone unit. The benzene and furyl rings are twisted slightly from each other, making a dihedral angle of 6.47 (7)°. Intramolecular C—H⋯O and C—H⋯Cl hydrogen bonds generate an S(5)S(5)S(5) ring motif. In the crystal structure, molecules are stacked along the b axis and weak intermolecular C—H⋯O hydrogen bonds are observed. |
format | Text |
id | pubmed-2962097 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29620972010-12-30 (E)-3-(2-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one Fun, Hoong-Kun Patil, P. S. Jebas, Samuel Robinson Dharmaprakash, S. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(9)ClO(2), adopts an E configuration with respect to the C=C double bond of the propenone unit. The benzene and furyl rings are twisted slightly from each other, making a dihedral angle of 6.47 (7)°. Intramolecular C—H⋯O and C—H⋯Cl hydrogen bonds generate an S(5)S(5)S(5) ring motif. In the crystal structure, molecules are stacked along the b axis and weak intermolecular C—H⋯O hydrogen bonds are observed. International Union of Crystallography 2008-07-12 /pmc/articles/PMC2962097/ /pubmed/21203181 http://dx.doi.org/10.1107/S1600536808020965 Text en © Fun 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 Fun, Hoong-Kun Patil, P. S. Jebas, Samuel Robinson Dharmaprakash, S. M. (E)-3-(2-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title | (E)-3-(2-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_full | (E)-3-(2-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_fullStr | (E)-3-(2-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_full_unstemmed | (E)-3-(2-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_short | (E)-3-(2-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_sort | (e)-3-(2-chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962097/ https://www.ncbi.nlm.nih.gov/pubmed/21203181 http://dx.doi.org/10.1107/S1600536808020965 |
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