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(E)-3-(2-Chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one
In the title molecule, C(21)H(16)ClNO(3), the quinoline and benzene rings are inclined at 56.96 (6)° with respect to each other and the dioxine ring is in a twist-chair conformation. The structure is devoid of any classical hydrogen bonds. Rather weak intermolecular hydrogen-bonding interactions...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983824/ https://www.ncbi.nlm.nih.gov/pubmed/21580589 http://dx.doi.org/10.1107/S1600536810007464 |
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author | Rizvi, Syed Umar Farooq Siddiqui, Hamid Latif Hussain, Tanvir Azam, Muhammad Parvez, Masood |
author_facet | Rizvi, Syed Umar Farooq Siddiqui, Hamid Latif Hussain, Tanvir Azam, Muhammad Parvez, Masood |
author_sort | Rizvi, Syed Umar Farooq |
collection | PubMed |
description | In the title molecule, C(21)H(16)ClNO(3), the quinoline and benzene rings are inclined at 56.96 (6)° with respect to each other and the dioxine ring is in a twist-chair conformation. The structure is devoid of any classical hydrogen bonds. Rather weak intermolecular hydrogen-bonding interactions of the types C—H⋯N and C—H⋯O are present, consolidating the crystal structure. |
format | Text |
id | pubmed-2983824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29838242010-12-30 (E)-3-(2-Chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one Rizvi, Syed Umar Farooq Siddiqui, Hamid Latif Hussain, Tanvir Azam, Muhammad Parvez, Masood Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title molecule, C(21)H(16)ClNO(3), the quinoline and benzene rings are inclined at 56.96 (6)° with respect to each other and the dioxine ring is in a twist-chair conformation. The structure is devoid of any classical hydrogen bonds. Rather weak intermolecular hydrogen-bonding interactions of the types C—H⋯N and C—H⋯O are present, consolidating the crystal structure. International Union of Crystallography 2010-03-03 /pmc/articles/PMC2983824/ /pubmed/21580589 http://dx.doi.org/10.1107/S1600536810007464 Text en © Rizvi et al. 2010 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 Rizvi, Syed Umar Farooq Siddiqui, Hamid Latif Hussain, Tanvir Azam, Muhammad Parvez, Masood (E)-3-(2-Chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one |
title | (E)-3-(2-Chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one |
title_full | (E)-3-(2-Chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one |
title_fullStr | (E)-3-(2-Chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one |
title_full_unstemmed | (E)-3-(2-Chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one |
title_short | (E)-3-(2-Chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one |
title_sort | (e)-3-(2-chloro-6-methyl-3-quinolyl)-1-(2,3-dihydro-1,4-benzodioxin-6-yl)prop-2-en-1-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983824/ https://www.ncbi.nlm.nih.gov/pubmed/21580589 http://dx.doi.org/10.1107/S1600536810007464 |
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