Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate

The title compound, a Schiff base, C(24)H(31)NO(3), has a substituted aromatic ring at both ends of the azomethine linkage and these make a dihedral angle of 24.9 (1)°. There is an intra­molecular hydrogen bond between the hy­droxy group (donor) and the N atom of themazomethine linkage.

Detalles Bibliográficos
Autores principales: Shakir, Raied Mustafa, Ariffin, Azhar, Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009105/
https://www.ncbi.nlm.nih.gov/pubmed/21589089
http://dx.doi.org/10.1107/S1600536810041383
_version_ 1782194607700836352
author Shakir, Raied Mustafa
Ariffin, Azhar
Ng, Seik Weng
author_facet Shakir, Raied Mustafa
Ariffin, Azhar
Ng, Seik Weng
author_sort Shakir, Raied Mustafa
collection PubMed
description The title compound, a Schiff base, C(24)H(31)NO(3), has a substituted aromatic ring at both ends of the azomethine linkage and these make a dihedral angle of 24.9 (1)°. There is an intra­molecular hydrogen bond between the hy­droxy group (donor) and the N atom of themazomethine linkage.
format Text
id pubmed-3009105
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30091052010-12-30 Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate Shakir, Raied Mustafa Ariffin, Azhar Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, a Schiff base, C(24)H(31)NO(3), has a substituted aromatic ring at both ends of the azomethine linkage and these make a dihedral angle of 24.9 (1)°. There is an intra­molecular hydrogen bond between the hy­droxy group (donor) and the N atom of themazomethine linkage. International Union of Crystallography 2010-10-23 /pmc/articles/PMC3009105/ /pubmed/21589089 http://dx.doi.org/10.1107/S1600536810041383 Text en © Shakir et al. 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
Shakir, Raied Mustafa
Ariffin, Azhar
Ng, Seik Weng
Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate
title Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate
title_full Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate
title_fullStr Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate
title_full_unstemmed Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate
title_short Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate
title_sort ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benzyl­idene)­amino]­benzoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009105/
https://www.ncbi.nlm.nih.gov/pubmed/21589089
http://dx.doi.org/10.1107/S1600536810041383
work_keys_str_mv AT shakirraiedmustafa ethyl435ditertbutyl2hydroxybenzylideneaminobenzoate
AT ariffinazhar ethyl435ditertbutyl2hydroxybenzylideneaminobenzoate
AT ngseikweng ethyl435ditertbutyl2hydroxybenzylideneaminobenzoate

Ejemplares similares