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3-Chloro-N-(4-methoxyphenyl)propanamide
The title compound, C(10)H(12)ClNO(2), is a halogenated derivative of a secondary amide bearing an aromatic substituent. The C(=O)—N(H)—C(ar)—C(ar) torsion angle of −33.70 (18)° rules out the presence of resonance spanning the amide as well as the aromatic system. In the crystal, classical N—H⋯O hyd...
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/PMC3247603/ https://www.ncbi.nlm.nih.gov/pubmed/22219908 http://dx.doi.org/10.1107/S1600536811040682 |
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author | Betz, Richard Gerber, Thomas Hosten, Eric Siddegowda, Maravanahalli S. Yathirajan, Hemmige S. |
author_facet | Betz, Richard Gerber, Thomas Hosten, Eric Siddegowda, Maravanahalli S. Yathirajan, Hemmige S. |
author_sort | Betz, Richard |
collection | PubMed |
description | The title compound, C(10)H(12)ClNO(2), is a halogenated derivative of a secondary amide bearing an aromatic substituent. The C(=O)—N(H)—C(ar)—C(ar) torsion angle of −33.70 (18)° rules out the presence of resonance spanning the amide as well as the aromatic system. In the crystal, classical N—H⋯O hydrogen bonds, as well as C–H⋯O contacts connect the molecules into chains propagating along the a axis. |
format | Online Article Text |
id | pubmed-3247603 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32476032012-01-04 3-Chloro-N-(4-methoxyphenyl)propanamide Betz, Richard Gerber, Thomas Hosten, Eric Siddegowda, Maravanahalli S. Yathirajan, Hemmige S. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(10)H(12)ClNO(2), is a halogenated derivative of a secondary amide bearing an aromatic substituent. The C(=O)—N(H)—C(ar)—C(ar) torsion angle of −33.70 (18)° rules out the presence of resonance spanning the amide as well as the aromatic system. In the crystal, classical N—H⋯O hydrogen bonds, as well as C–H⋯O contacts connect the molecules into chains propagating along the a axis. International Union of Crystallography 2011-10-08 /pmc/articles/PMC3247603/ /pubmed/22219908 http://dx.doi.org/10.1107/S1600536811040682 Text en © Betz 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 Betz, Richard Gerber, Thomas Hosten, Eric Siddegowda, Maravanahalli S. Yathirajan, Hemmige S. 3-Chloro-N-(4-methoxyphenyl)propanamide |
title | 3-Chloro-N-(4-methoxyphenyl)propanamide |
title_full | 3-Chloro-N-(4-methoxyphenyl)propanamide |
title_fullStr | 3-Chloro-N-(4-methoxyphenyl)propanamide |
title_full_unstemmed | 3-Chloro-N-(4-methoxyphenyl)propanamide |
title_short | 3-Chloro-N-(4-methoxyphenyl)propanamide |
title_sort | 3-chloro-n-(4-methoxyphenyl)propanamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247603/ https://www.ncbi.nlm.nih.gov/pubmed/22219908 http://dx.doi.org/10.1107/S1600536811040682 |
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