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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...

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Detalles Bibliográficos
Autores principales: Betz, Richard, Gerber, Thomas, Hosten, Eric, Siddegowda, Maravanahalli S., Yathirajan, Hemmige S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
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.
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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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