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1-Cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1H-pyrazole-4-carb­oxy­lic acid

In the title compound, C(17)H(20)N(2)O(3), the meth­oxy­phenyl unit is disordered over two sets of sites in a 0.715 (4):0.285 (4) ratio. The pyrazole ring forms dihedral angles of 55.88 (16) and 72.6 (4)° with the benzene rings of its major and minor components, respectively. The cyclo­hexane ring a...

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Autores principales: Fun, Hoong-Kun, Quah, Ching Kheng, Chandrakantha, B., Isloor, A. M., Shetty, Prakash
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239134/
https://www.ncbi.nlm.nih.gov/pubmed/22199982
http://dx.doi.org/10.1107/S1600536811050872
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author Fun, Hoong-Kun
Quah, Ching Kheng
Chandrakantha, B.
Isloor, A. M.
Shetty, Prakash
author_facet Fun, Hoong-Kun
Quah, Ching Kheng
Chandrakantha, B.
Isloor, A. M.
Shetty, Prakash
author_sort Fun, Hoong-Kun
collection PubMed
description In the title compound, C(17)H(20)N(2)O(3), the meth­oxy­phenyl unit is disordered over two sets of sites in a 0.715 (4):0.285 (4) ratio. The pyrazole ring forms dihedral angles of 55.88 (16) and 72.6 (4)° with the benzene rings of its major and minor components, respectively. The cyclo­hexane ring adopts a chair conformation and its C—N bond is in an equatorial orientation. In the crystal, mol­ecules are linked into inversion dimers by pairs of O—H⋯O hydrogen bonds, generating R (2) (2)(8) loops.
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spelling pubmed-32391342011-12-23 1-Cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1H-pyrazole-4-carb­oxy­lic acid Fun, Hoong-Kun Quah, Ching Kheng Chandrakantha, B. Isloor, A. M. Shetty, Prakash Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(20)N(2)O(3), the meth­oxy­phenyl unit is disordered over two sets of sites in a 0.715 (4):0.285 (4) ratio. The pyrazole ring forms dihedral angles of 55.88 (16) and 72.6 (4)° with the benzene rings of its major and minor components, respectively. The cyclo­hexane ring adopts a chair conformation and its C—N bond is in an equatorial orientation. In the crystal, mol­ecules are linked into inversion dimers by pairs of O—H⋯O hydrogen bonds, generating R (2) (2)(8) loops. International Union of Crystallography 2011-11-30 /pmc/articles/PMC3239134/ /pubmed/22199982 http://dx.doi.org/10.1107/S1600536811050872 Text en © Fun 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
Fun, Hoong-Kun
Quah, Ching Kheng
Chandrakantha, B.
Isloor, A. M.
Shetty, Prakash
1-Cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1H-pyrazole-4-carb­oxy­lic acid
title 1-Cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1H-pyrazole-4-carb­oxy­lic acid
title_full 1-Cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1H-pyrazole-4-carb­oxy­lic acid
title_fullStr 1-Cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1H-pyrazole-4-carb­oxy­lic acid
title_full_unstemmed 1-Cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1H-pyrazole-4-carb­oxy­lic acid
title_short 1-Cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1H-pyrazole-4-carb­oxy­lic acid
title_sort 1-cyclo­hexyl-5-(4-meth­oxy­phen­yl)-1h-pyrazole-4-carb­oxy­lic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239134/
https://www.ncbi.nlm.nih.gov/pubmed/22199982
http://dx.doi.org/10.1107/S1600536811050872
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