1,1′-Bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate

The title compound, C(26)H(28)O(4), lies about a crystallographic twofold rotation axis. The cyclo­hexane rings adopt a chair conformation. The two benzene rings form a dihedral angle of 40.82 (3)°. No significant intra- or inter­molecular inter­actions are observed in the crystal structure.

Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Quah, Ching Kheng, Wu, Dongdong, Zhang, Yan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379232/
https://www.ncbi.nlm.nih.gov/pubmed/22719430
http://dx.doi.org/10.1107/S1600536812018478
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author Fun, Hoong-Kun
Quah, Ching Kheng
Wu, Dongdong
Zhang, Yan
author_facet Fun, Hoong-Kun
Quah, Ching Kheng
Wu, Dongdong
Zhang, Yan
author_sort Fun, Hoong-Kun
collection PubMed
description The title compound, C(26)H(28)O(4), lies about a crystallographic twofold rotation axis. The cyclo­hexane rings adopt a chair conformation. The two benzene rings form a dihedral angle of 40.82 (3)°. No significant intra- or inter­molecular inter­actions are observed in the crystal structure.
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spelling pubmed-33792322012-06-20 1,1′-Bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate Fun, Hoong-Kun Quah, Ching Kheng Wu, Dongdong Zhang, Yan Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(26)H(28)O(4), lies about a crystallographic twofold rotation axis. The cyclo­hexane rings adopt a chair conformation. The two benzene rings form a dihedral angle of 40.82 (3)°. No significant intra- or inter­molecular inter­actions are observed in the crystal structure. International Union of Crystallography 2012-05-05 /pmc/articles/PMC3379232/ /pubmed/22719430 http://dx.doi.org/10.1107/S1600536812018478 Text en © Fun et al. 2012 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
Wu, Dongdong
Zhang, Yan
1,1′-Bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate
title 1,1′-Bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate
title_full 1,1′-Bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate
title_fullStr 1,1′-Bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate
title_full_unstemmed 1,1′-Bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate
title_short 1,1′-Bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate
title_sort 1,1′-bicyclo­hexyl-1,1′-diyl 1,1′-biphenyl-2,2′-dicarboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3379232/
https://www.ncbi.nlm.nih.gov/pubmed/22719430
http://dx.doi.org/10.1107/S1600536812018478
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AT wudongdong 11bicyclohexyl11diyl11biphenyl22dicarboxylate
AT zhangyan 11bicyclohexyl11diyl11biphenyl22dicarboxylate

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