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3,5-Dimeth­oxy-4′-methyl­biphen­yl

The title compound, C(15)H(16)O(2), crystallizes with three independent mol­ecules in the asymmetric unit. The intra­molecular torsion angle between the aromatic rings of each mol­ecule are −36.4 (3), 41.3 (3) and −37.8 (3)°. In the crystal, the complicated packing of the mol­ecules forms wave-like...

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Detalles Bibliográficos
Autores principales: Lahtinen, Manu, Nättinen, Kalle, Nummelin, Sami
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629539/
https://www.ncbi.nlm.nih.gov/pubmed/23634057
http://dx.doi.org/10.1107/S1600536813006053
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author Lahtinen, Manu
Nättinen, Kalle
Nummelin, Sami
author_facet Lahtinen, Manu
Nättinen, Kalle
Nummelin, Sami
author_sort Lahtinen, Manu
collection PubMed
description The title compound, C(15)H(16)O(2), crystallizes with three independent mol­ecules in the asymmetric unit. The intra­molecular torsion angle between the aromatic rings of each mol­ecule are −36.4 (3), 41.3 (3) and −37.8 (3)°. In the crystal, the complicated packing of the mol­ecules forms wave-like layers along the b and c axes. The mol­ecules are connected via extensive meth­oxy–phenyl C—H⋯π inter­actions. A weak C—H⋯O hydrogen-bonding network also exists between meth­oxy O atoms and aromatic or meth­oxy H atoms.
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spelling pubmed-36295392013-04-30 3,5-Dimeth­oxy-4′-methyl­biphen­yl Lahtinen, Manu Nättinen, Kalle Nummelin, Sami Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(16)O(2), crystallizes with three independent mol­ecules in the asymmetric unit. The intra­molecular torsion angle between the aromatic rings of each mol­ecule are −36.4 (3), 41.3 (3) and −37.8 (3)°. In the crystal, the complicated packing of the mol­ecules forms wave-like layers along the b and c axes. The mol­ecules are connected via extensive meth­oxy–phenyl C—H⋯π inter­actions. A weak C—H⋯O hydrogen-bonding network also exists between meth­oxy O atoms and aromatic or meth­oxy H atoms. International Union of Crystallography 2013-03-09 /pmc/articles/PMC3629539/ /pubmed/23634057 http://dx.doi.org/10.1107/S1600536813006053 Text en © Lahtinen et al. 2013 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
Lahtinen, Manu
Nättinen, Kalle
Nummelin, Sami
3,5-Dimeth­oxy-4′-methyl­biphen­yl
title 3,5-Dimeth­oxy-4′-methyl­biphen­yl
title_full 3,5-Dimeth­oxy-4′-methyl­biphen­yl
title_fullStr 3,5-Dimeth­oxy-4′-methyl­biphen­yl
title_full_unstemmed 3,5-Dimeth­oxy-4′-methyl­biphen­yl
title_short 3,5-Dimeth­oxy-4′-methyl­biphen­yl
title_sort 3,5-dimeth­oxy-4′-methyl­biphen­yl
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3629539/
https://www.ncbi.nlm.nih.gov/pubmed/23634057
http://dx.doi.org/10.1107/S1600536813006053
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