2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.

In the title mol-ecule, C(11)H(14)BrNO(2), there is twist between the mean plane of the amide group and the benzene ring [the C-N-C-C torsion angle is -172.1 (2)°]. The amide H atom forms an intra-molecular hydrogen bond with the Br atom. In the crystal, inter-molecular O-H⋯O and weak C-H⋯O hydrogen...

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Autores:
Grande Tovar, Carlos
Kennedy, Alan R.
Zuluaga, Fabio
Quintero, David E.
Moreno Fuquen, Rodolfo
Tipo de recurso:
Article of investigation
Fecha de publicación:
2011
Institución:
Universidad ICESI
Repositorio:
Repositorio ICESI
Idioma:
eng
OAI Identifier:
oai:repository.icesi.edu.co:10906/79854
Acceso en línea:
http://www.ncbi.nlm.nih.gov/pubmed/22065656
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC3200793
http://journals.iucr.org/e/issues/2011/09/00/tk2780/tk2780.pdf
http://hdl.handle.net/10906/79854
Palabra clave:
Biología
Molécula
Bromo
Ácido bórico
Métodos de investigación en bioquímica
Biochemistry research
Rights
openAccess
License
https://creativecommons.org/licenses/by-nc-nd/4.0/
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repository_id_str
spelling Grande Tovar, CarlosKennedy, Alan R.Zuluaga, FabioQuintero, David E.Moreno Fuquen, Rodolfo2016-08-30T22:01:47Z2016-08-30T22:01:47Z2011-09-0110.1107/S16005368110331501600-5368http://www.ncbi.nlm.nih.gov/pubmed/22065656http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC3200793http://journals.iucr.org/e/issues/2011/09/00/tk2780/tk2780.pdfhttp://hdl.handle.net/10906/79854instname: Universidad Icesireponame: Biblioteca Digitalrepourl: https://repository.icesi.edu.co/In the title mol-ecule, C(11)H(14)BrNO(2), there is twist between the mean plane of the amide group and the benzene ring [the C-N-C-C torsion angle is -172.1 (2)°]. The amide H atom forms an intra-molecular hydrogen bond with the Br atom. In the crystal, inter-molecular O-H⋯O and weak C-H⋯O hydrogen bonds link mol-ecules into a chain along [100].7 páginasengInternational Union of CrystallographyActa Crystallographica Section E: Structure Reports Online, Vol. 67 - 2011EL AUTOR, expresa que la obra objeto de la presente autorización es original y la elaboró sin quebrantar ni suplantar los derechos de autor de terceros, y de tal forma, la obra es de su exclusiva autoría y tiene la titularidad sobre éste. PARÁGRAFO: en caso de queja o acción por parte de un tercero referente a los derechos de autor sobre el artículo, folleto o libro en cuestión, EL AUTOR, asumirá la responsabilidad total, y saldrá en defensa de los derechos aquí autorizados; para todos los efectos, la Universidad Icesi actúa como un tercero de buena fe. Esta autorización, permite a la Universidad Icesi, de forma indefinida, para que en los términos establecidos en la Ley 23 de 1982, la Ley 44 de 1993, leyes y jurisprudencia vigente al respecto, haga publicación de este con fines educativos. Toda persona que consulte ya sea la biblioteca o en medio electrónico podrá copiar apartes del texto citando siempre la fuentes, es decir el título del trabajo y el autor.https://creativecommons.org/licenses/by-nc-nd/4.0/info:eu-repo/semantics/openAccessAtribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)http://purl.org/coar/access_right/c_abf2BiologíaMoléculaBromoÁcido bóricoMétodos de investigación en bioquímicaBiochemistry research2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.info:eu-repo/semantics/articlehttp://purl.org/coar/resource_type/c_2df8fbb1Artículoinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/version/c_970fb48d4fbd8a85Comunidad Universidad Icesi – Investigadores6717TEXTgrande_bromo_n_2011.pdf.txtgrande_bromo_n_2011.pdf.txttext/plain14929http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/79854/2/grande_bromo_n_2011.pdf.txt2e88f8f7f5b23e0ac7069efe776b53ccMD52grande_bromo_droxy_2011.pdf.txtgrande_bromo_droxy_2011.pdf.txttext/plain14929http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/79854/3/grande_bromo_droxy_2011.pdf.txt2e88f8f7f5b23e0ac7069efe776b53ccMD53ORIGINALgrande_bromo_droxy_2011.pdfgrande_bromo_droxy_2011.pdfapplication/pdf286518http://repository.icesi.edu.co/biblioteca_digital/bitstream/10906/79854/1/grande_bromo_droxy_2011.pdf4cfc5a0d8300ae4fc72cc8bb2925990bMD5110906/79854oai:repository.icesi.edu.co:10906/798542020-05-20 21:46:45.018Biblioteca Digital - Universidad icesicdcriollo@icesi.edu.co
dc.title.spa.fl_str_mv 2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.
title 2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.
spellingShingle 2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.
Biología
Molécula
Bromo
Ácido bórico
Métodos de investigación en bioquímica
Biochemistry research
title_short 2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.
title_full 2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.
title_fullStr 2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.
title_full_unstemmed 2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.
title_sort 2-Bromo-N-(2-hy-droxy-5-methyl-phen-yl)-2-methyl-propanamide.
dc.creator.fl_str_mv Grande Tovar, Carlos
Kennedy, Alan R.
Zuluaga, Fabio
Quintero, David E.
Moreno Fuquen, Rodolfo
dc.contributor.author.spa.fl_str_mv Grande Tovar, Carlos
Kennedy, Alan R.
Zuluaga, Fabio
Quintero, David E.
Moreno Fuquen, Rodolfo
dc.subject.none.fl_str_mv Biología
Molécula
Bromo
Ácido bórico
Métodos de investigación en bioquímica
topic Biología
Molécula
Bromo
Ácido bórico
Métodos de investigación en bioquímica
Biochemistry research
dc.subject.spa.fl_str_mv Biochemistry research
description In the title mol-ecule, C(11)H(14)BrNO(2), there is twist between the mean plane of the amide group and the benzene ring [the C-N-C-C torsion angle is -172.1 (2)°]. The amide H atom forms an intra-molecular hydrogen bond with the Br atom. In the crystal, inter-molecular O-H⋯O and weak C-H⋯O hydrogen bonds link mol-ecules into a chain along [100].
publishDate 2011
dc.date.issued.none.fl_str_mv 2011-09-01
dc.date.accessioned.none.fl_str_mv 2016-08-30T22:01:47Z
dc.date.available.none.fl_str_mv 2016-08-30T22:01:47Z
dc.type.none.fl_str_mv info:eu-repo/semantics/article
dc.type.coar.none.fl_str_mv http://purl.org/coar/resource_type/c_2df8fbb1
dc.type.local.none.fl_str_mv Artículo
dc.type.version.none.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.spa.fl_str_mv 10.1107/S1600536811033150
dc.identifier.issn.none.fl_str_mv 1600-5368
dc.identifier.other.spa.fl_str_mv http://www.ncbi.nlm.nih.gov/pubmed/22065656
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC3200793
dc.identifier.other.none.fl_str_mv http://journals.iucr.org/e/issues/2011/09/00/tk2780/tk2780.pdf
dc.identifier.uri.none.fl_str_mv http://hdl.handle.net/10906/79854
dc.identifier.instname.none.fl_str_mv instname: Universidad Icesi
dc.identifier.reponame.none.fl_str_mv reponame: Biblioteca Digital
dc.identifier.repourl.none.fl_str_mv repourl: https://repository.icesi.edu.co/
identifier_str_mv 10.1107/S1600536811033150
1600-5368
instname: Universidad Icesi
reponame: Biblioteca Digital
repourl: https://repository.icesi.edu.co/
url http://www.ncbi.nlm.nih.gov/pubmed/22065656
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=PMC3200793
http://journals.iucr.org/e/issues/2011/09/00/tk2780/tk2780.pdf
http://hdl.handle.net/10906/79854
dc.language.iso.eng.fl_str_mv eng
language eng
dc.relation.ispartof.none.fl_str_mv Acta Crystallographica Section E: Structure Reports Online, Vol. 67 - 2011
dc.rights.uri.none.fl_str_mv https://creativecommons.org/licenses/by-nc-nd/4.0/
dc.rights.accessrights.none.fl_str_mv info:eu-repo/semantics/openAccess
dc.rights.license.none.fl_str_mv Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
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Atribución-NoComercial-SinDerivadas 4.0 Internacional (CC BY-NC-ND 4.0)
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eu_rights_str_mv openAccess
dc.format.extent.none.fl_str_mv 7 páginas
dc.publisher.spa.fl_str_mv International Union of Crystallography
institution Universidad ICESI
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