2-Bromo-4-chloro-6-[(E)-o-tolyl­imino­meth­yl]phenol

The title compound, C(14)H(11)BrClNO, is a Schiff base compound derived from the condensation of 3-bromo-5-chloro­salicyl­aldehyde and o-toluidine in methanol. The aromatic rings make a dihedral angle of 38.3 (1)°. The mol­ecular conformation is stabilized by an intra­molecular O—H⋯N hydrogen bond,...

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Detalles Bibliográficos
Autor principal: Guo, Jin-Bao
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983373/
https://www.ncbi.nlm.nih.gov/pubmed/21587657
http://dx.doi.org/10.1107/S1600536810037931
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author Guo, Jin-Bao
author_facet Guo, Jin-Bao
author_sort Guo, Jin-Bao
collection PubMed
description The title compound, C(14)H(11)BrClNO, is a Schiff base compound derived from the condensation of 3-bromo-5-chloro­salicyl­aldehyde and o-toluidine in methanol. The aromatic rings make a dihedral angle of 38.3 (1)°. The mol­ecular conformation is stabilized by an intra­molecular O—H⋯N hydrogen bond, generating an S(6) ring.
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spelling pubmed-29833732010-12-30 2-Bromo-4-chloro-6-[(E)-o-tolyl­imino­meth­yl]phenol Guo, Jin-Bao Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(11)BrClNO, is a Schiff base compound derived from the condensation of 3-bromo-5-chloro­salicyl­aldehyde and o-toluidine in methanol. The aromatic rings make a dihedral angle of 38.3 (1)°. The mol­ecular conformation is stabilized by an intra­molecular O—H⋯N hydrogen bond, generating an S(6) ring. International Union of Crystallography 2010-09-30 /pmc/articles/PMC2983373/ /pubmed/21587657 http://dx.doi.org/10.1107/S1600536810037931 Text en © Jin-Bao Guo 2010 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
Guo, Jin-Bao
2-Bromo-4-chloro-6-[(E)-o-tolyl­imino­meth­yl]phenol
title 2-Bromo-4-chloro-6-[(E)-o-tolyl­imino­meth­yl]phenol
title_full 2-Bromo-4-chloro-6-[(E)-o-tolyl­imino­meth­yl]phenol
title_fullStr 2-Bromo-4-chloro-6-[(E)-o-tolyl­imino­meth­yl]phenol
title_full_unstemmed 2-Bromo-4-chloro-6-[(E)-o-tolyl­imino­meth­yl]phenol
title_short 2-Bromo-4-chloro-6-[(E)-o-tolyl­imino­meth­yl]phenol
title_sort 2-bromo-4-chloro-6-[(e)-o-tolyl­imino­meth­yl]phenol
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983373/
https://www.ncbi.nlm.nih.gov/pubmed/21587657
http://dx.doi.org/10.1107/S1600536810037931
work_keys_str_mv AT guojinbao 2bromo4chloro6eotolyliminomethylphenol

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