2-Chloro-N-(3,5-dimethyl­phen­yl)acetamide

The conformation of the C=O bond in the structure of the title compound, C(10)H(12)ClNO, is anti to the N—H bond and to the C—Cl bond in the side chain in all four independent mol­ecules comprising the asymmetric unit. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into sup...

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Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Foro, Sabine, Terao, Hiromitsu, Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977723/
https://www.ncbi.nlm.nih.gov/pubmed/21583859
http://dx.doi.org/10.1107/S160053680901304X
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author Gowda, B. Thimme
Foro, Sabine
Terao, Hiromitsu
Fuess, Hartmut
author_facet Gowda, B. Thimme
Foro, Sabine
Terao, Hiromitsu
Fuess, Hartmut
author_sort Gowda, B. Thimme
collection PubMed
description The conformation of the C=O bond in the structure of the title compound, C(10)H(12)ClNO, is anti to the N—H bond and to the C—Cl bond in the side chain in all four independent mol­ecules comprising the asymmetric unit. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into supra­molecular chains
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spelling pubmed-29777232010-12-30 2-Chloro-N-(3,5-dimethyl­phen­yl)acetamide Gowda, B. Thimme Foro, Sabine Terao, Hiromitsu Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The conformation of the C=O bond in the structure of the title compound, C(10)H(12)ClNO, is anti to the N—H bond and to the C—Cl bond in the side chain in all four independent mol­ecules comprising the asymmetric unit. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into supra­molecular chains International Union of Crystallography 2009-04-18 /pmc/articles/PMC2977723/ /pubmed/21583859 http://dx.doi.org/10.1107/S160053680901304X Text en © Gowda 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
Gowda, B. Thimme
Foro, Sabine
Terao, Hiromitsu
Fuess, Hartmut
2-Chloro-N-(3,5-dimethyl­phen­yl)acetamide
title 2-Chloro-N-(3,5-dimethyl­phen­yl)acetamide
title_full 2-Chloro-N-(3,5-dimethyl­phen­yl)acetamide
title_fullStr 2-Chloro-N-(3,5-dimethyl­phen­yl)acetamide
title_full_unstemmed 2-Chloro-N-(3,5-dimethyl­phen­yl)acetamide
title_short 2-Chloro-N-(3,5-dimethyl­phen­yl)acetamide
title_sort 2-chloro-n-(3,5-dimethyl­phen­yl)acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977723/
https://www.ncbi.nlm.nih.gov/pubmed/21583859
http://dx.doi.org/10.1107/S160053680901304X
work_keys_str_mv AT gowdabthimme 2chloron35dimethylphenylacetamide
AT forosabine 2chloron35dimethylphenylacetamide
AT teraohiromitsu 2chloron35dimethylphenylacetamide
AT fuesshartmut 2chloron35dimethylphenylacetamide

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