trans-2-(2-Nitro-1-phenyl­eth­yl)cyclo­hexa­none

In the title compound, C(14)H(17)NO(3), the plane of the phenyl ring and the least-squares plane of the cyclo­hexyl moiety enclose an angle of 89.14 (6)°. The cyclohexyl ring adopts a chair conformation. In the crystal, the molecules are linked by weak C—H⋯O bonds, with each of the nitro-O atoms acc...

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Detalles Bibliográficos
Autores principales: Zenz, Ivo, Mayr, Herbert, Mayer, Peter
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011465/
https://www.ncbi.nlm.nih.gov/pubmed/21589437
http://dx.doi.org/10.1107/S1600536810045423
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author Zenz, Ivo
Mayr, Herbert
Mayer, Peter
author_facet Zenz, Ivo
Mayr, Herbert
Mayer, Peter
author_sort Zenz, Ivo
collection PubMed
description In the title compound, C(14)H(17)NO(3), the plane of the phenyl ring and the least-squares plane of the cyclo­hexyl moiety enclose an angle of 89.14 (6)°. The cyclohexyl ring adopts a chair conformation. In the crystal, the molecules are linked by weak C—H⋯O bonds, with each of the nitro-O atoms accepting two such interactions.
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spelling pubmed-30114652010-12-30 trans-2-(2-Nitro-1-phenyl­eth­yl)cyclo­hexa­none Zenz, Ivo Mayr, Herbert Mayer, Peter Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(17)NO(3), the plane of the phenyl ring and the least-squares plane of the cyclo­hexyl moiety enclose an angle of 89.14 (6)°. The cyclohexyl ring adopts a chair conformation. In the crystal, the molecules are linked by weak C—H⋯O bonds, with each of the nitro-O atoms accepting two such interactions. International Union of Crystallography 2010-11-13 /pmc/articles/PMC3011465/ /pubmed/21589437 http://dx.doi.org/10.1107/S1600536810045423 Text en © Zenz 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
Zenz, Ivo
Mayr, Herbert
Mayer, Peter
trans-2-(2-Nitro-1-phenyl­eth­yl)cyclo­hexa­none
title trans-2-(2-Nitro-1-phenyl­eth­yl)cyclo­hexa­none
title_full trans-2-(2-Nitro-1-phenyl­eth­yl)cyclo­hexa­none
title_fullStr trans-2-(2-Nitro-1-phenyl­eth­yl)cyclo­hexa­none
title_full_unstemmed trans-2-(2-Nitro-1-phenyl­eth­yl)cyclo­hexa­none
title_short trans-2-(2-Nitro-1-phenyl­eth­yl)cyclo­hexa­none
title_sort trans-2-(2-nitro-1-phenyl­eth­yl)cyclo­hexa­none
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011465/
https://www.ncbi.nlm.nih.gov/pubmed/21589437
http://dx.doi.org/10.1107/S1600536810045423
work_keys_str_mv AT zenzivo trans22nitro1phenylethylcyclohexanone
AT mayrherbert trans22nitro1phenylethylcyclohexanone
AT mayerpeter trans22nitro1phenylethylcyclohexanone

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