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2-Meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2H-1-benzopyran-4-one

The title mol­ecule, C(20)H(21)NO(6), adopts a keto–amine tautomeric form. An intra­molecular N—H⋯O hydrogen bond, classified as a resonanse-assisted hydrogen bond, influences the mol­ecular conformation; the two benzene rings form a dihedral angle of 24.6 (1)°. In the crystal structure, weak inter­...

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Detalles Bibliográficos
Autores principales: Małecka, Magdalena, Ciołkowski, Michał, Budzisz, Elżbieta
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980241/
https://www.ncbi.nlm.nih.gov/pubmed/21580127
http://dx.doi.org/10.1107/S1600536809054889
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author Małecka, Magdalena
Ciołkowski, Michał
Budzisz, Elżbieta
author_facet Małecka, Magdalena
Ciołkowski, Michał
Budzisz, Elżbieta
author_sort Małecka, Magdalena
collection PubMed
description The title mol­ecule, C(20)H(21)NO(6), adopts a keto–amine tautomeric form. An intra­molecular N—H⋯O hydrogen bond, classified as a resonanse-assisted hydrogen bond, influences the mol­ecular conformation; the two benzene rings form a dihedral angle of 24.6 (1)°. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules into chains propagating along [001].
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spelling pubmed-29802412010-12-30 2-Meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2H-1-benzopyran-4-one Małecka, Magdalena Ciołkowski, Michał Budzisz, Elżbieta Acta Crystallogr Sect E Struct Rep Online Organic Papers The title mol­ecule, C(20)H(21)NO(6), adopts a keto–amine tautomeric form. An intra­molecular N—H⋯O hydrogen bond, classified as a resonanse-assisted hydrogen bond, influences the mol­ecular conformation; the two benzene rings form a dihedral angle of 24.6 (1)°. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules into chains propagating along [001]. International Union of Crystallography 2009-12-24 /pmc/articles/PMC2980241/ /pubmed/21580127 http://dx.doi.org/10.1107/S1600536809054889 Text en © Małecka 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
Małecka, Magdalena
Ciołkowski, Michał
Budzisz, Elżbieta
2-Meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2H-1-benzopyran-4-one
title 2-Meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2H-1-benzopyran-4-one
title_full 2-Meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2H-1-benzopyran-4-one
title_fullStr 2-Meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2H-1-benzopyran-4-one
title_full_unstemmed 2-Meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2H-1-benzopyran-4-one
title_short 2-Meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2H-1-benzopyran-4-one
title_sort 2-meth­oxy-3-[(3,4,5-trimethoxy­anilino)methyl­idene]-3,4-dihydro-2h-1-benzopyran-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980241/
https://www.ncbi.nlm.nih.gov/pubmed/21580127
http://dx.doi.org/10.1107/S1600536809054889
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AT ciołkowskimichał 2methoxy3345trimethoxyanilinomethylidene34dihydro2h1benzopyran4one
AT budziszelzbieta 2methoxy3345trimethoxyanilinomethylidene34dihydro2h1benzopyran4one