2,3-Bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene

The mol­ecule of the title compound, C(20)H(22)O(2), a symmetrically 2-methyl­phenol-substituted divinyl analog, exhibits crystallographically imposed C (2) symmetry. The mol­ecular structure is essentially planar. The structure is stabilized by a short inter­molecular C—H⋯O contact. Cooperative C—H...

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Detalles Bibliográficos
Autores principales: Sathiyanarayanan, K., George Fernand, A., Dhanasekaran, V., Rathore, R. S.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2007
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915193/
https://www.ncbi.nlm.nih.gov/pubmed/21200687
http://dx.doi.org/10.1107/S1600536807063398
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author Sathiyanarayanan, K.
George Fernand, A.
Dhanasekaran, V.
Rathore, R. S.
author_facet Sathiyanarayanan, K.
George Fernand, A.
Dhanasekaran, V.
Rathore, R. S.
author_sort Sathiyanarayanan, K.
collection PubMed
description The mol­ecule of the title compound, C(20)H(22)O(2), a symmetrically 2-methyl­phenol-substituted divinyl analog, exhibits crystallographically imposed C (2) symmetry. The mol­ecular structure is essentially planar. The structure is stabilized by a short inter­molecular C—H⋯O contact. Cooperative C—H⋯π inter­actions generate an infinite one-dimensional chain of mol­ecules along the a axis.
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spelling pubmed-29151932010-12-30 2,3-Bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene Sathiyanarayanan, K. George Fernand, A. Dhanasekaran, V. Rathore, R. S. Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(20)H(22)O(2), a symmetrically 2-methyl­phenol-substituted divinyl analog, exhibits crystallographically imposed C (2) symmetry. The mol­ecular structure is essentially planar. The structure is stabilized by a short inter­molecular C—H⋯O contact. Cooperative C—H⋯π inter­actions generate an infinite one-dimensional chain of mol­ecules along the a axis. International Union of Crystallography 2007-12-06 /pmc/articles/PMC2915193/ /pubmed/21200687 http://dx.doi.org/10.1107/S1600536807063398 Text en © International Union of Crystallography 2008 http://journals.iucr.org/services/termsofuse.html This is an open-access article distributed under the terms described at http://journals.iucr.org/services/termsofuse.html.
spellingShingle Organic Papers
Sathiyanarayanan, K.
George Fernand, A.
Dhanasekaran, V.
Rathore, R. S.
2,3-Bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene
title 2,3-Bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene
title_full 2,3-Bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene
title_fullStr 2,3-Bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene
title_full_unstemmed 2,3-Bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene
title_short 2,3-Bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene
title_sort 2,3-bis[(2-methyl­phen­oxy)meth­yl]buta-1,3-diene
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2915193/
https://www.ncbi.nlm.nih.gov/pubmed/21200687
http://dx.doi.org/10.1107/S1600536807063398
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AT dhanasekaranv 23bis2methylphenoxymethylbuta13diene
AT rathorers 23bis2methylphenoxymethylbuta13diene

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