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(E)-N′-(3-Benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide

In the title compound, C(21)H(19)N(3)O(3), the pyridine ring forms a dihedral angle of 15.25 (6)° with the benzene ring. The dihedral angle between the two benzene rings is 83.66 (7)°. The meth­oxy group is slightly twisted away from the attached ring [C—O—C—C = 7.5 (2)°]. In the crystal structure,...

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Detalles Bibliográficos
Autores principales: Naveenkumar, H. S., Sadikun, Amirin, Ibrahim, Pazilah, Loh, Wan-Sin, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970303/
https://www.ncbi.nlm.nih.gov/pubmed/21577984
http://dx.doi.org/10.1107/S1600536809037921
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author Naveenkumar, H. S.
Sadikun, Amirin
Ibrahim, Pazilah
Loh, Wan-Sin
Fun, Hoong-Kun
author_facet Naveenkumar, H. S.
Sadikun, Amirin
Ibrahim, Pazilah
Loh, Wan-Sin
Fun, Hoong-Kun
author_sort Naveenkumar, H. S.
collection PubMed
description In the title compound, C(21)H(19)N(3)O(3), the pyridine ring forms a dihedral angle of 15.25 (6)° with the benzene ring. The dihedral angle between the two benzene rings is 83.66 (7)°. The meth­oxy group is slightly twisted away from the attached ring [C—O—C—C = 7.5 (2)°]. In the crystal structure, mol­ecules are linked into a three-dimensional network by inter­molecular N—H⋯N and C—H⋯O hydrogen bonds. The structure is further stabilized by C—H⋯π inter­actions.
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spelling pubmed-29703032010-12-30 (E)-N′-(3-Benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide Naveenkumar, H. S. Sadikun, Amirin Ibrahim, Pazilah Loh, Wan-Sin Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(19)N(3)O(3), the pyridine ring forms a dihedral angle of 15.25 (6)° with the benzene ring. The dihedral angle between the two benzene rings is 83.66 (7)°. The meth­oxy group is slightly twisted away from the attached ring [C—O—C—C = 7.5 (2)°]. In the crystal structure, mol­ecules are linked into a three-dimensional network by inter­molecular N—H⋯N and C—H⋯O hydrogen bonds. The structure is further stabilized by C—H⋯π inter­actions. International Union of Crystallography 2009-09-26 /pmc/articles/PMC2970303/ /pubmed/21577984 http://dx.doi.org/10.1107/S1600536809037921 Text en © Naveenkumar et al. 2009 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
Naveenkumar, H. S.
Sadikun, Amirin
Ibrahim, Pazilah
Loh, Wan-Sin
Fun, Hoong-Kun
(E)-N′-(3-Benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide
title (E)-N′-(3-Benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide
title_full (E)-N′-(3-Benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide
title_fullStr (E)-N′-(3-Benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide
title_full_unstemmed (E)-N′-(3-Benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide
title_short (E)-N′-(3-Benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide
title_sort (e)-n′-(3-benz­yloxy-4-methoxy­benzyl­idene)isonicotinohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970303/
https://www.ncbi.nlm.nih.gov/pubmed/21577984
http://dx.doi.org/10.1107/S1600536809037921
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