(2E)-2-(3,4-Di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2H)-one

In the title chalcone derivative, C(19)H(18)O(3), the cyclo­hexa­none ring adopts a distorted half-chair conformation and the dihedral angle between the aromatic rings is 52.20 (15)°. In the crystal, weak C—H⋯O hydrogen bonds link the mol­ecules into C(12) [001] chains. [Image: see text]

Detalles Bibliográficos
Autores principales: Shirmila, D. Angeline, Jonathan, D. Reuben, Priya, M. Krishna, Hemalatha, J., Usha, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2021
Materias:
Data Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462320/
https://www.ncbi.nlm.nih.gov/pubmed/36340292
http://dx.doi.org/10.1107/S2414314621003096
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author Shirmila, D. Angeline
Jonathan, D. Reuben
Priya, M. Krishna
Hemalatha, J.
Usha, G.
author_facet Shirmila, D. Angeline
Jonathan, D. Reuben
Priya, M. Krishna
Hemalatha, J.
Usha, G.
author_sort Shirmila, D. Angeline
collection PubMed
description In the title chalcone derivative, C(19)H(18)O(3), the cyclo­hexa­none ring adopts a distorted half-chair conformation and the dihedral angle between the aromatic rings is 52.20 (15)°. In the crystal, weak C—H⋯O hydrogen bonds link the mol­ecules into C(12) [001] chains. [Image: see text]
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spelling pubmed-94623202022-11-04 (2E)-2-(3,4-Di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2H)-one Shirmila, D. Angeline Jonathan, D. Reuben Priya, M. Krishna Hemalatha, J. Usha, G. IUCrdata Data Reports In the title chalcone derivative, C(19)H(18)O(3), the cyclo­hexa­none ring adopts a distorted half-chair conformation and the dihedral angle between the aromatic rings is 52.20 (15)°. In the crystal, weak C—H⋯O hydrogen bonds link the mol­ecules into C(12) [001] chains. [Image: see text] International Union of Crystallography 2021-03-26 /pmc/articles/PMC9462320/ /pubmed/36340292 http://dx.doi.org/10.1107/S2414314621003096 Text en © Shirmila et al. 2021 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Data Reports
Shirmila, D. Angeline
Jonathan, D. Reuben
Priya, M. Krishna
Hemalatha, J.
Usha, G.
(2E)-2-(3,4-Di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2H)-one
title (2E)-2-(3,4-Di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2H)-one
title_full (2E)-2-(3,4-Di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2H)-one
title_fullStr (2E)-2-(3,4-Di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2H)-one
title_full_unstemmed (2E)-2-(3,4-Di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2H)-one
title_short (2E)-2-(3,4-Di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2H)-one
title_sort (2e)-2-(3,4-di­meth­oxy­benzyl­idene)-3,4-di­hydro­naphthalen-1(2h)-one
topic Data Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462320/
https://www.ncbi.nlm.nih.gov/pubmed/36340292
http://dx.doi.org/10.1107/S2414314621003096
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