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2-[(E)-(2-Chlorophenyl)iminomethyl]-6-methylphenol
The title compound, C(14)H(12)ClNO, a Schiff base derived from 3-methylsalicylaldehyde, crystallizes in the phenol–imine tautomeric form with an E conformation for the imine functionality. The molecule is not planar, the dihedral angle between the aromatic rings being 36.38 (5)°. The hydroxy H a...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008053/ https://www.ncbi.nlm.nih.gov/pubmed/21588779 http://dx.doi.org/10.1107/S1600536810033969 |
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author | Zhu, Peihua Yu, Jiemei Wang, Hongyan Zhang, Chunlai Yang, Dongming |
author_facet | Zhu, Peihua Yu, Jiemei Wang, Hongyan Zhang, Chunlai Yang, Dongming |
author_sort | Zhu, Peihua |
collection | PubMed |
description | The title compound, C(14)H(12)ClNO, a Schiff base derived from 3-methylsalicylaldehyde, crystallizes in the phenol–imine tautomeric form with an E conformation for the imine functionality. The molecule is not planar, the dihedral angle between the aromatic rings being 36.38 (5)°. The hydroxy H atom is involved in a strong intramolecular O—H⋯N hydrogen bond, generating an S(6) ring. |
format | Text |
id | pubmed-3008053 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30080532010-12-30 2-[(E)-(2-Chlorophenyl)iminomethyl]-6-methylphenol Zhu, Peihua Yu, Jiemei Wang, Hongyan Zhang, Chunlai Yang, Dongming Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(12)ClNO, a Schiff base derived from 3-methylsalicylaldehyde, crystallizes in the phenol–imine tautomeric form with an E conformation for the imine functionality. The molecule is not planar, the dihedral angle between the aromatic rings being 36.38 (5)°. The hydroxy H atom is involved in a strong intramolecular O—H⋯N hydrogen bond, generating an S(6) ring. International Union of Crystallography 2010-08-28 /pmc/articles/PMC3008053/ /pubmed/21588779 http://dx.doi.org/10.1107/S1600536810033969 Text en © Zhu 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 Zhu, Peihua Yu, Jiemei Wang, Hongyan Zhang, Chunlai Yang, Dongming 2-[(E)-(2-Chlorophenyl)iminomethyl]-6-methylphenol |
title | 2-[(E)-(2-Chlorophenyl)iminomethyl]-6-methylphenol |
title_full | 2-[(E)-(2-Chlorophenyl)iminomethyl]-6-methylphenol |
title_fullStr | 2-[(E)-(2-Chlorophenyl)iminomethyl]-6-methylphenol |
title_full_unstemmed | 2-[(E)-(2-Chlorophenyl)iminomethyl]-6-methylphenol |
title_short | 2-[(E)-(2-Chlorophenyl)iminomethyl]-6-methylphenol |
title_sort | 2-[(e)-(2-chlorophenyl)iminomethyl]-6-methylphenol |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3008053/ https://www.ncbi.nlm.nih.gov/pubmed/21588779 http://dx.doi.org/10.1107/S1600536810033969 |
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