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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...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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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. |
format | Text |
id | pubmed-2977650 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT gowdabthimme 2chloron3chlorophenylacetamide AT forosabine 2chloron3chlorophenylacetamide AT teraohiromitsu 2chloron3chlorophenylacetamide AT fuesshartmut 2chloron3chlorophenylacetamide |