N-Cyclo­hexyl­benzamide

The structure of the title compound, C(13)H(17)NO, features an anti disposition of the N—H and carbonyl groups. The amide group is twisted with respect to the benzene ring [N–C(=O)–C–C torsion angle = −30.8 (4)°]. In the crystal, C(4) chains propagating in [100] are formed by inter­molecular N–H⋯O h...

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Detalles Bibliográficos
Autores principales: Khan, Islam Ullah, Javaid, Rashid, Sharif, Shahzad, Tiekink, Edward R. T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007063/
https://www.ncbi.nlm.nih.gov/pubmed/21587911
http://dx.doi.org/10.1107/S1600536810022609
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author Khan, Islam Ullah
Javaid, Rashid
Sharif, Shahzad
Tiekink, Edward R. T.
author_facet Khan, Islam Ullah
Javaid, Rashid
Sharif, Shahzad
Tiekink, Edward R. T.
author_sort Khan, Islam Ullah
collection PubMed
description The structure of the title compound, C(13)H(17)NO, features an anti disposition of the N—H and carbonyl groups. The amide group is twisted with respect to the benzene ring [N–C(=O)–C–C torsion angle = −30.8 (4)°]. In the crystal, C(4) chains propagating in [100] are formed by inter­molecular N–H⋯O hydrogen bonds. Weak C—H⋯π inter­actions link the chains into sheets.
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spelling pubmed-30070632010-12-30 N-Cyclo­hexyl­benzamide Khan, Islam Ullah Javaid, Rashid Sharif, Shahzad Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers The structure of the title compound, C(13)H(17)NO, features an anti disposition of the N—H and carbonyl groups. The amide group is twisted with respect to the benzene ring [N–C(=O)–C–C torsion angle = −30.8 (4)°]. In the crystal, C(4) chains propagating in [100] are formed by inter­molecular N–H⋯O hydrogen bonds. Weak C—H⋯π inter­actions link the chains into sheets. International Union of Crystallography 2010-06-18 /pmc/articles/PMC3007063/ /pubmed/21587911 http://dx.doi.org/10.1107/S1600536810022609 Text en © Khan et al. 2010 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
Khan, Islam Ullah
Javaid, Rashid
Sharif, Shahzad
Tiekink, Edward R. T.
N-Cyclo­hexyl­benzamide
title N-Cyclo­hexyl­benzamide
title_full N-Cyclo­hexyl­benzamide
title_fullStr N-Cyclo­hexyl­benzamide
title_full_unstemmed N-Cyclo­hexyl­benzamide
title_short N-Cyclo­hexyl­benzamide
title_sort n-cyclo­hexyl­benzamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007063/
https://www.ncbi.nlm.nih.gov/pubmed/21587911
http://dx.doi.org/10.1107/S1600536810022609
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AT javaidrashid ncyclohexylbenzamide
AT sharifshahzad ncyclohexylbenzamide
AT tiekinkedwardrt ncyclohexylbenzamide

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