2-tert-Butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol

The asymmetric unit of the title Schiff base compound, C(18)H(27)NO(2), contains two independent mol­ecules in which the C=N bond lengths are 1.278 (2) and 1.280 (2) Å and the cyclo­hexane rings adopt chair conformations. Intra­molecular O—H⋯N hydrogen bonding between hy­droxy and imine groups and w...

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Autores principales: Jamjah, Roghayieh, Nekoomanesh, Mehdi, Pourjafar, Tayebeh, Zohuri, Gholam Hossein, Afshartaromi, Faramarz, Notash, Behrouz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152047/
https://www.ncbi.nlm.nih.gov/pubmed/21837152
http://dx.doi.org/10.1107/S1600536811023385
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author Jamjah, Roghayieh
Nekoomanesh, Mehdi
Pourjafar, Tayebeh
Zohuri, Gholam Hossein
Afshartaromi, Faramarz
Notash, Behrouz
author_facet Jamjah, Roghayieh
Nekoomanesh, Mehdi
Pourjafar, Tayebeh
Zohuri, Gholam Hossein
Afshartaromi, Faramarz
Notash, Behrouz
author_sort Jamjah, Roghayieh
collection PubMed
description The asymmetric unit of the title Schiff base compound, C(18)H(27)NO(2), contains two independent mol­ecules in which the C=N bond lengths are 1.278 (2) and 1.280 (2) Å and the cyclo­hexane rings adopt chair conformations. Intra­molecular O—H⋯N hydrogen bonding between hy­droxy and imine groups and weak C—H⋯O hydrogen bonds help to stabilize the mol­ecular structure.
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spelling pubmed-31520472011-08-11 2-tert-Butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol Jamjah, Roghayieh Nekoomanesh, Mehdi Pourjafar, Tayebeh Zohuri, Gholam Hossein Afshartaromi, Faramarz Notash, Behrouz Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title Schiff base compound, C(18)H(27)NO(2), contains two independent mol­ecules in which the C=N bond lengths are 1.278 (2) and 1.280 (2) Å and the cyclo­hexane rings adopt chair conformations. Intra­molecular O—H⋯N hydrogen bonding between hy­droxy and imine groups and weak C—H⋯O hydrogen bonds help to stabilize the mol­ecular structure. International Union of Crystallography 2011-06-22 /pmc/articles/PMC3152047/ /pubmed/21837152 http://dx.doi.org/10.1107/S1600536811023385 Text en © Jamjah et al. 2011 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
Jamjah, Roghayieh
Nekoomanesh, Mehdi
Pourjafar, Tayebeh
Zohuri, Gholam Hossein
Afshartaromi, Faramarz
Notash, Behrouz
2-tert-Butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol
title 2-tert-Butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol
title_full 2-tert-Butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol
title_fullStr 2-tert-Butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol
title_full_unstemmed 2-tert-Butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol
title_short 2-tert-Butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol
title_sort 2-tert-butyl-6-(cyclo­hexyl­imino­meth­yl)-4-meth­oxy­phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152047/
https://www.ncbi.nlm.nih.gov/pubmed/21837152
http://dx.doi.org/10.1107/S1600536811023385
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