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(2E,6E)-2,6-Bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none

The title compound, C(20)H(14)Cl(4)O, was prepared by the reaction of 2,6-dichloro­benzaldehyde and cyclo­hexa­none. In the mol­ecule, the central cyclo­hexa­none ring adopts an envelope conformation, while the terminal benzene rings make a dihedral angle of 57.87 (9)°.

Detalles Bibliográficos
Autores principales: Mahdavinia, Gholam Hossein, Mirzazadeh, Maryam, Amani, Vahid, Notash, Behrouz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297849/
https://www.ncbi.nlm.nih.gov/pubmed/22412652
http://dx.doi.org/10.1107/S1600536812006629
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author Mahdavinia, Gholam Hossein
Mirzazadeh, Maryam
Amani, Vahid
Notash, Behrouz
author_facet Mahdavinia, Gholam Hossein
Mirzazadeh, Maryam
Amani, Vahid
Notash, Behrouz
author_sort Mahdavinia, Gholam Hossein
collection PubMed
description The title compound, C(20)H(14)Cl(4)O, was prepared by the reaction of 2,6-dichloro­benzaldehyde and cyclo­hexa­none. In the mol­ecule, the central cyclo­hexa­none ring adopts an envelope conformation, while the terminal benzene rings make a dihedral angle of 57.87 (9)°.
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spelling pubmed-32978492012-03-12 (2E,6E)-2,6-Bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none Mahdavinia, Gholam Hossein Mirzazadeh, Maryam Amani, Vahid Notash, Behrouz Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(20)H(14)Cl(4)O, was prepared by the reaction of 2,6-dichloro­benzaldehyde and cyclo­hexa­none. In the mol­ecule, the central cyclo­hexa­none ring adopts an envelope conformation, while the terminal benzene rings make a dihedral angle of 57.87 (9)°. International Union of Crystallography 2012-02-17 /pmc/articles/PMC3297849/ /pubmed/22412652 http://dx.doi.org/10.1107/S1600536812006629 Text en © Mahdavinia 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
Mahdavinia, Gholam Hossein
Mirzazadeh, Maryam
Amani, Vahid
Notash, Behrouz
(2E,6E)-2,6-Bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none
title (2E,6E)-2,6-Bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none
title_full (2E,6E)-2,6-Bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none
title_fullStr (2E,6E)-2,6-Bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none
title_full_unstemmed (2E,6E)-2,6-Bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none
title_short (2E,6E)-2,6-Bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none
title_sort (2e,6e)-2,6-bis(2,6-dichloro­benzyl­idene)­cyclo­hexa­none
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297849/
https://www.ncbi.nlm.nih.gov/pubmed/22412652
http://dx.doi.org/10.1107/S1600536812006629
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