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(E)-16-(4-Chloro­benzyl­idene)estrone

In the title compound, C(25)H(25)ClO(2), the C ring adopts a chair conformation, while the B ring approximates a half-chair conformation. The five-membered ring D has a twist con­form­ation on the C—C bond fused with the C ring. Aromatic rings A and E are not coplanar, as evidenced by the dihedral a...

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Autores principales: Suresh, J., Thenmozhi, H., Jeyachandran, Veerappan, Kumar, R. Ranjith, Lakshman, P. L. Nilantha
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588250/
https://www.ncbi.nlm.nih.gov/pubmed/23476374
http://dx.doi.org/10.1107/S1600536812050349
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author Suresh, J.
Thenmozhi, H.
Jeyachandran, Veerappan
Kumar, R. Ranjith
Lakshman, P. L. Nilantha
author_facet Suresh, J.
Thenmozhi, H.
Jeyachandran, Veerappan
Kumar, R. Ranjith
Lakshman, P. L. Nilantha
author_sort Suresh, J.
collection PubMed
description In the title compound, C(25)H(25)ClO(2), the C ring adopts a chair conformation, while the B ring approximates a half-chair conformation. The five-membered ring D has a twist con­form­ation on the C—C bond fused with the C ring. Aromatic rings A and E are not coplanar, as evidenced by the dihedral angle of 7.51 (1)°. In the crystal, O—H⋯O hydrogen bonds form a double chain along the ab plane inter­connected by C—H⋯O inter­actions.
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spelling pubmed-35882502013-03-08 (E)-16-(4-Chloro­benzyl­idene)estrone Suresh, J. Thenmozhi, H. Jeyachandran, Veerappan Kumar, R. Ranjith Lakshman, P. L. Nilantha Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(25)H(25)ClO(2), the C ring adopts a chair conformation, while the B ring approximates a half-chair conformation. The five-membered ring D has a twist con­form­ation on the C—C bond fused with the C ring. Aromatic rings A and E are not coplanar, as evidenced by the dihedral angle of 7.51 (1)°. In the crystal, O—H⋯O hydrogen bonds form a double chain along the ab plane inter­connected by C—H⋯O inter­actions. International Union of Crystallography 2012-12-19 /pmc/articles/PMC3588250/ /pubmed/23476374 http://dx.doi.org/10.1107/S1600536812050349 Text en © Suresh 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
Suresh, J.
Thenmozhi, H.
Jeyachandran, Veerappan
Kumar, R. Ranjith
Lakshman, P. L. Nilantha
(E)-16-(4-Chloro­benzyl­idene)estrone
title (E)-16-(4-Chloro­benzyl­idene)estrone
title_full (E)-16-(4-Chloro­benzyl­idene)estrone
title_fullStr (E)-16-(4-Chloro­benzyl­idene)estrone
title_full_unstemmed (E)-16-(4-Chloro­benzyl­idene)estrone
title_short (E)-16-(4-Chloro­benzyl­idene)estrone
title_sort (e)-16-(4-chloro­benzyl­idene)estrone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588250/
https://www.ncbi.nlm.nih.gov/pubmed/23476374
http://dx.doi.org/10.1107/S1600536812050349
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