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(E)-3-(4-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one
In the title molecule, C(13)H(9)ClO(2), the benzene and furyl rings are slightly twisted from each other with a dihedral angle of 5.1 (1)°. An intramolecular C—H⋯O hydrogen-bond interaction generates an S(5) ring motif. In the crystal structure, molecules are stacked along the b axis and the cry...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962155/ https://www.ncbi.nlm.nih.gov/pubmed/21203235 http://dx.doi.org/10.1107/S1600536808021934 |
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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 | In the title molecule, C(13)H(9)ClO(2), the benzene and furyl rings are slightly twisted from each other with a dihedral angle of 5.1 (1)°. An intramolecular C—H⋯O hydrogen-bond interaction generates an S(5) ring motif. In the crystal structure, molecules are stacked along the b axis and the crystal packing is stabilized by weak intermolecular C—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-2962155 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29621552010-12-30 (E)-3-(4-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 In the title molecule, C(13)H(9)ClO(2), the benzene and furyl rings are slightly twisted from each other with a dihedral angle of 5.1 (1)°. An intramolecular C—H⋯O hydrogen-bond interaction generates an S(5) ring motif. In the crystal structure, molecules are stacked along the b axis and the crystal packing is stabilized by weak intermolecular C—H⋯O hydrogen bonds. International Union of Crystallography 2008-07-19 /pmc/articles/PMC2962155/ /pubmed/21203235 http://dx.doi.org/10.1107/S1600536808021934 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-(4-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title | (E)-3-(4-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_full | (E)-3-(4-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_fullStr | (E)-3-(4-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_full_unstemmed | (E)-3-(4-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_short | (E)-3-(4-Chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
title_sort | (e)-3-(4-chlorophenyl)-1-(2-furyl)prop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962155/ https://www.ncbi.nlm.nih.gov/pubmed/21203235 http://dx.doi.org/10.1107/S1600536808021934 |
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