Cargando…

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

The title amine, C(24)H(33)NO(3), has two substituted aromatic rings at either end of the –CH(2)NH– linkage [C(ar­yl)–CH(2)–NH–C(ar­yl) torsion angle = 77.4 (3)°]. The amino and hy­droxy groups are hydrogen-bond donors to the carbonyl O atom of an adjacent mol­ecule. These hydrogen bonds give rise t...

Descripción completa

Detalles Bibliográficos
Autores principales: Shakir, Raied Mustafa, Ariffin, Azhar, Ng, Seik Weng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009098/
https://www.ncbi.nlm.nih.gov/pubmed/21589090
http://dx.doi.org/10.1107/S1600536810040742
_version_ 1782194605631995904
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 amine, C(24)H(33)NO(3), has two substituted aromatic rings at either end of the –CH(2)NH– linkage [C(ar­yl)–CH(2)–NH–C(ar­yl) torsion angle = 77.4 (3)°]. The amino and hy­droxy groups are hydrogen-bond donors to the carbonyl O atom of an adjacent mol­ecule. These hydrogen bonds give rise to a chain that runs along the b axis. One of the tert-butyl groups is disordered over two positions with a site-occupation factor of 0.834 (6) for the major occupied site.
format Text
id pubmed-3009098
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30090982010-12-30 Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benz­yl)amino]­benzoate Shakir, Raied Mustafa Ariffin, Azhar Ng, Seik Weng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title amine, C(24)H(33)NO(3), has two substituted aromatic rings at either end of the –CH(2)NH– linkage [C(ar­yl)–CH(2)–NH–C(ar­yl) torsion angle = 77.4 (3)°]. The amino and hy­droxy groups are hydrogen-bond donors to the carbonyl O atom of an adjacent mol­ecule. These hydrogen bonds give rise to a chain that runs along the b axis. One of the tert-butyl groups is disordered over two positions with a site-occupation factor of 0.834 (6) for the major occupied site. International Union of Crystallography 2010-10-23 /pmc/articles/PMC3009098/ /pubmed/21589090 http://dx.doi.org/10.1107/S1600536810040742 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-hy­droxy­benz­yl)amino]­benzoate
title Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benz­yl)amino]­benzoate
title_full Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benz­yl)amino]­benzoate
title_fullStr Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benz­yl)amino]­benzoate
title_full_unstemmed Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benz­yl)amino]­benzoate
title_short Ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benz­yl)amino]­benzoate
title_sort ethyl 4-[(3,5-di-tert-butyl-2-hy­droxy­benz­yl)amino]­benzoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009098/
https://www.ncbi.nlm.nih.gov/pubmed/21589090
http://dx.doi.org/10.1107/S1600536810040742
work_keys_str_mv AT shakirraiedmustafa ethyl435ditertbutyl2hydroxybenzylaminobenzoate
AT ariffinazhar ethyl435ditertbutyl2hydroxybenzylaminobenzoate
AT ngseikweng ethyl435ditertbutyl2hydroxybenzylaminobenzoate