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4-[(4-Methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2H-chromen-2-one

The title compound, C(26)H(24)N(2)O(2), was prepared from the reaction of 4-chloro-3-formyl­coumarin with p-methyl­benzyl­amine. Even though there are no strong and specific inter­actions in the crystal structure, the translationally related mol­ecules form chains along the b axis. The coumarin moie...

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Detalles Bibliográficos
Autores principales: Rambabu, D., Rama Krishna, G., Malla Reddy, C., Pal, Manojit
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009000/
https://www.ncbi.nlm.nih.gov/pubmed/21589052
http://dx.doi.org/10.1107/S1600536810041218
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author Rambabu, D.
Rama Krishna, G.
Malla Reddy, C.
Pal, Manojit
author_facet Rambabu, D.
Rama Krishna, G.
Malla Reddy, C.
Pal, Manojit
author_sort Rambabu, D.
collection PubMed
description The title compound, C(26)H(24)N(2)O(2), was prepared from the reaction of 4-chloro-3-formyl­coumarin with p-methyl­benzyl­amine. Even though there are no strong and specific inter­actions in the crystal structure, the translationally related mol­ecules form chains along the b axis. The coumarin moieties are stacked through π–π inter­actions [centroid–centroid distance = 3.5275 (7) Å], forming layers perpendicular to the stacking direction.
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spelling pubmed-30090002010-12-30 4-[(4-Methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2H-chromen-2-one Rambabu, D. Rama Krishna, G. Malla Reddy, C. Pal, Manojit Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(26)H(24)N(2)O(2), was prepared from the reaction of 4-chloro-3-formyl­coumarin with p-methyl­benzyl­amine. Even though there are no strong and specific inter­actions in the crystal structure, the translationally related mol­ecules form chains along the b axis. The coumarin moieties are stacked through π–π inter­actions [centroid–centroid distance = 3.5275 (7) Å], forming layers perpendicular to the stacking direction. International Union of Crystallography 2010-10-20 /pmc/articles/PMC3009000/ /pubmed/21589052 http://dx.doi.org/10.1107/S1600536810041218 Text en © Rambabu 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
Rambabu, D.
Rama Krishna, G.
Malla Reddy, C.
Pal, Manojit
4-[(4-Methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2H-chromen-2-one
title 4-[(4-Methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2H-chromen-2-one
title_full 4-[(4-Methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2H-chromen-2-one
title_fullStr 4-[(4-Methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2H-chromen-2-one
title_full_unstemmed 4-[(4-Methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2H-chromen-2-one
title_short 4-[(4-Methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2H-chromen-2-one
title_sort 4-[(4-methyl­benz­yl)amino]-3-[(4-methyl­benz­yl)imino­meth­yl]-2h-chromen-2-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3009000/
https://www.ncbi.nlm.nih.gov/pubmed/21589052
http://dx.doi.org/10.1107/S1600536810041218
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