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(2E)-1-(2,5-Dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one
In the title compound, C(17)H(15)NO(5), an intramolecular C—H⋯O hydrogen bond generates an S(6) ring motif. The benzene rings form a dihedral angle of 6.45 (7)° with each other. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(8) loops. Adjacent dimers are...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247450/ https://www.ncbi.nlm.nih.gov/pubmed/22220068 http://dx.doi.org/10.1107/S1600536811043224 |
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author | Fun, Hoong-Kun Chia, Tze Shyang Narayana, B. Nayak, Prakash S. Sarojini, B. K. |
author_facet | Fun, Hoong-Kun Chia, Tze Shyang Narayana, B. Nayak, Prakash S. Sarojini, B. K. |
author_sort | Fun, Hoong-Kun |
collection | PubMed |
description | In the title compound, C(17)H(15)NO(5), an intramolecular C—H⋯O hydrogen bond generates an S(6) ring motif. The benzene rings form a dihedral angle of 6.45 (7)° with each other. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(8) loops. Adjacent dimers are further connected by C—H⋯O hydrogen bonds into an infinite chain along the [011] direction. |
format | Online Article Text |
id | pubmed-3247450 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32474502012-01-04 (2E)-1-(2,5-Dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one Fun, Hoong-Kun Chia, Tze Shyang Narayana, B. Nayak, Prakash S. Sarojini, B. K. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(15)NO(5), an intramolecular C—H⋯O hydrogen bond generates an S(6) ring motif. The benzene rings form a dihedral angle of 6.45 (7)° with each other. In the crystal, inversion dimers linked by pairs of C—H⋯O hydrogen bonds generate R (2) (2)(8) loops. Adjacent dimers are further connected by C—H⋯O hydrogen bonds into an infinite chain along the [011] direction. International Union of Crystallography 2011-10-29 /pmc/articles/PMC3247450/ /pubmed/22220068 http://dx.doi.org/10.1107/S1600536811043224 Text en © Fun et al. 2011 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 Chia, Tze Shyang Narayana, B. Nayak, Prakash S. Sarojini, B. K. (2E)-1-(2,5-Dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one |
title | (2E)-1-(2,5-Dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one |
title_full | (2E)-1-(2,5-Dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one |
title_fullStr | (2E)-1-(2,5-Dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one |
title_full_unstemmed | (2E)-1-(2,5-Dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one |
title_short | (2E)-1-(2,5-Dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one |
title_sort | (2e)-1-(2,5-dimethoxyphenyl)-3-(3-nitrophenyl)prop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247450/ https://www.ncbi.nlm.nih.gov/pubmed/22220068 http://dx.doi.org/10.1107/S1600536811043224 |
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