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N-Cyclohexyl-3,4,5-trimethoxybenzamide
The 3,5-methoxy groups in the title compound, C(16)H(23)NO(4), are almost coplanar with the aromatic ring, whereas the 4-methoxy group is bent out of this plane. The three CH(3)—O—C—C torsion angles are −1.51 (18), 0.73 (19) and 75.33 (15)°. The cyclohexane ring adopts a chair conformation. In th...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972029/ https://www.ncbi.nlm.nih.gov/pubmed/21578939 http://dx.doi.org/10.1107/S1600536809050284 |
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author | Saeed, Aamer Arshad, Muhammad Khera, Rasheed Ahmad Bolte, Michael |
author_facet | Saeed, Aamer Arshad, Muhammad Khera, Rasheed Ahmad Bolte, Michael |
author_sort | Saeed, Aamer |
collection | PubMed |
description | The 3,5-methoxy groups in the title compound, C(16)H(23)NO(4), are almost coplanar with the aromatic ring, whereas the 4-methoxy group is bent out of this plane. The three CH(3)—O—C—C torsion angles are −1.51 (18), 0.73 (19) and 75.33 (15)°. The cyclohexane ring adopts a chair conformation. In the crystal, molecules are connected by intermolecular N—H⋯O hydrogen bonds into chains running along the b axis. |
format | Text |
id | pubmed-2972029 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29720292010-12-30 N-Cyclohexyl-3,4,5-trimethoxybenzamide Saeed, Aamer Arshad, Muhammad Khera, Rasheed Ahmad Bolte, Michael Acta Crystallogr Sect E Struct Rep Online Organic Papers The 3,5-methoxy groups in the title compound, C(16)H(23)NO(4), are almost coplanar with the aromatic ring, whereas the 4-methoxy group is bent out of this plane. The three CH(3)—O—C—C torsion angles are −1.51 (18), 0.73 (19) and 75.33 (15)°. The cyclohexane ring adopts a chair conformation. In the crystal, molecules are connected by intermolecular N—H⋯O hydrogen bonds into chains running along the b axis. International Union of Crystallography 2009-11-28 /pmc/articles/PMC2972029/ /pubmed/21578939 http://dx.doi.org/10.1107/S1600536809050284 Text en © Saeed et al. 2009 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 Saeed, Aamer Arshad, Muhammad Khera, Rasheed Ahmad Bolte, Michael N-Cyclohexyl-3,4,5-trimethoxybenzamide |
title |
N-Cyclohexyl-3,4,5-trimethoxybenzamide |
title_full |
N-Cyclohexyl-3,4,5-trimethoxybenzamide |
title_fullStr |
N-Cyclohexyl-3,4,5-trimethoxybenzamide |
title_full_unstemmed |
N-Cyclohexyl-3,4,5-trimethoxybenzamide |
title_short |
N-Cyclohexyl-3,4,5-trimethoxybenzamide |
title_sort | n-cyclohexyl-3,4,5-trimethoxybenzamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2972029/ https://www.ncbi.nlm.nih.gov/pubmed/21578939 http://dx.doi.org/10.1107/S1600536809050284 |
work_keys_str_mv | AT saeedaamer ncyclohexyl345trimethoxybenzamide AT arshadmuhammad ncyclohexyl345trimethoxybenzamide AT kherarasheedahmad ncyclohexyl345trimethoxybenzamide AT boltemichael ncyclohexyl345trimethoxybenzamide |