N-(3-Bromo­phen­yl)acetamide

The conformation of the N—H bond in the structure of the title compound, C(8)H(8)BrNO, is anti to the C=O bond and to the meta-bromo substituent of the aromatic ring in both independent mol­ecules comprising the asymmetric unit. Mol­ecules are linked through N—H⋯O hydrogen bonding into supra­molecul...

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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/PMC2977722/
https://www.ncbi.nlm.nih.gov/pubmed/21583858
http://dx.doi.org/10.1107/S1600536809013294
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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 N—H bond in the structure of the title compound, C(8)H(8)BrNO, is anti to the C=O bond and to the meta-bromo substituent of the aromatic ring in both independent mol­ecules comprising the asymmetric unit. Mol­ecules are linked through N—H⋯O hydrogen bonding into supra­molecular chains with a twisted topology.
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spelling pubmed-29777222010-12-30 N-(3-Bromo­phen­yl)acetamide Gowda, B. Thimme Foro, Sabine Terao, Hiromitsu Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The conformation of the N—H bond in the structure of the title compound, C(8)H(8)BrNO, is anti to the C=O bond and to the meta-bromo substituent of the aromatic ring in both independent mol­ecules comprising the asymmetric unit. Mol­ecules are linked through N—H⋯O hydrogen bonding into supra­molecular chains with a twisted topology. International Union of Crystallography 2009-04-18 /pmc/articles/PMC2977722/ /pubmed/21583858 http://dx.doi.org/10.1107/S1600536809013294 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
N-(3-Bromo­phen­yl)acetamide
title N-(3-Bromo­phen­yl)acetamide
title_full N-(3-Bromo­phen­yl)acetamide
title_fullStr N-(3-Bromo­phen­yl)acetamide
title_full_unstemmed N-(3-Bromo­phen­yl)acetamide
title_short N-(3-Bromo­phen­yl)acetamide
title_sort n-(3-bromo­phen­yl)acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977722/
https://www.ncbi.nlm.nih.gov/pubmed/21583858
http://dx.doi.org/10.1107/S1600536809013294
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AT forosabine n3bromophenylacetamide
AT teraohiromitsu n3bromophenylacetamide
AT fuesshartmut n3bromophenylacetamide

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