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2-Chloro-N-(3-chloro­phen­yl)acetamide

The N—H bond in the title compound, C(8)H(7)Cl(2)NO, is anti to the meta-chloro substituent in the aromatic ring in both independent mol­ecules comprising the asymmetric unit. The C=O bond is anti to the N—H bond and is also anti to the methyl­ene H atoms. Inter­molecular N—H⋯O hydrogen bonds link t...

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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:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977650/
https://www.ncbi.nlm.nih.gov/pubmed/21583993
http://dx.doi.org/10.1107/S1600536809011660
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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 N—H bond in the title compound, C(8)H(7)Cl(2)NO, is anti to the meta-chloro substituent in the aromatic ring in both independent mol­ecules comprising the asymmetric unit. The C=O bond is anti to the N—H bond and is also anti to the methyl­ene H atoms. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into supra­molecular chains.
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spelling pubmed-29776502010-12-30 2-Chloro-N-(3-chloro­phen­yl)acetamide Gowda, B. Thimme Foro, Sabine Terao, Hiromitsu Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The N—H bond in the title compound, C(8)H(7)Cl(2)NO, is anti to the meta-chloro substituent in the aromatic ring in both independent mol­ecules comprising the asymmetric unit. The C=O bond is anti to the N—H bond and is also anti to the methyl­ene H atoms. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into supra­molecular chains. International Union of Crystallography 2009-04-02 /pmc/articles/PMC2977650/ /pubmed/21583993 http://dx.doi.org/10.1107/S1600536809011660 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-chloro­phen­yl)acetamide
title 2-Chloro-N-(3-chloro­phen­yl)acetamide
title_full 2-Chloro-N-(3-chloro­phen­yl)acetamide
title_fullStr 2-Chloro-N-(3-chloro­phen­yl)acetamide
title_full_unstemmed 2-Chloro-N-(3-chloro­phen­yl)acetamide
title_short 2-Chloro-N-(3-chloro­phen­yl)acetamide
title_sort 2-chloro-n-(3-chloro­phen­yl)acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977650/
https://www.ncbi.nlm.nih.gov/pubmed/21583993
http://dx.doi.org/10.1107/S1600536809011660
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