3-Chloro-N′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide

The title compound, C(18)H(13)ClN(2)O(2), was prepared by the reaction of 2-hy­droxy-1-naphthaldehyde with 3-chloro­benzohydrazide in methanol. An intra­molecular O—H⋯N hydrogen bond influences the mol­ecular conformation; the benzene ring and naphthyl ring system form a dihedral angle of 17.1 (3)°....

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Detalles Bibliográficos
Autores principales: Li, Tian-Yi, Li, Wei
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051679/
https://www.ncbi.nlm.nih.gov/pubmed/21523050
http://dx.doi.org/10.1107/S1600536811000912
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author Li, Tian-Yi
Li, Wei
author_facet Li, Tian-Yi
Li, Wei
author_sort Li, Tian-Yi
collection PubMed
description The title compound, C(18)H(13)ClN(2)O(2), was prepared by the reaction of 2-hy­droxy-1-naphthaldehyde with 3-chloro­benzohydrazide in methanol. An intra­molecular O—H⋯N hydrogen bond influences the mol­ecular conformation; the benzene ring and naphthyl ring system form a dihedral angle of 17.1 (3)°. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains propagated in [101].
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spelling pubmed-30516792011-04-26 3-Chloro-N′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide Li, Tian-Yi Li, Wei Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(18)H(13)ClN(2)O(2), was prepared by the reaction of 2-hy­droxy-1-naphthaldehyde with 3-chloro­benzohydrazide in methanol. An intra­molecular O—H⋯N hydrogen bond influences the mol­ecular conformation; the benzene ring and naphthyl ring system form a dihedral angle of 17.1 (3)°. In the crystal, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains propagated in [101]. International Union of Crystallography 2011-01-12 /pmc/articles/PMC3051679/ /pubmed/21523050 http://dx.doi.org/10.1107/S1600536811000912 Text en © Li and Li 2011 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
Li, Tian-Yi
Li, Wei
3-Chloro-N′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide
title 3-Chloro-N′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide
title_full 3-Chloro-N′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide
title_fullStr 3-Chloro-N′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide
title_full_unstemmed 3-Chloro-N′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide
title_short 3-Chloro-N′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide
title_sort 3-chloro-n′-[(2-hy­droxy­naphthalen-1-yl)methyl­idene]benzohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051679/
https://www.ncbi.nlm.nih.gov/pubmed/21523050
http://dx.doi.org/10.1107/S1600536811000912
work_keys_str_mv AT litianyi 3chloron2hydroxynaphthalen1ylmethylidenebenzohydrazide
AT liwei 3chloron2hydroxynaphthalen1ylmethylidenebenzohydrazide

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