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N-(4-Chlorophenyl)-4-methylpyridin-2-amine
In the title compound, C(12)H(11)ClN(2), the dihedral angle between the benzene and pyridyl rings is 48.03 (8)°. Twists are also evident in the molecule, in particular about the N(a)–C(b) (a = amine and b = benzene) bond [C—N—C—C = −144.79 (18)°]. In the crystal, inversion dimers linked by pairs of...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007248/ https://www.ncbi.nlm.nih.gov/pubmed/21588463 http://dx.doi.org/10.1107/S1600536810030138 |
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author | Fairuz, Zainal A. Aiyub, Zaharah Abdullah, Zanariah Ng, Seik Weng Tiekink, Edward R. T. |
author_facet | Fairuz, Zainal A. Aiyub, Zaharah Abdullah, Zanariah Ng, Seik Weng Tiekink, Edward R. T. |
author_sort | Fairuz, Zainal A. |
collection | PubMed |
description | In the title compound, C(12)H(11)ClN(2), the dihedral angle between the benzene and pyridyl rings is 48.03 (8)°. Twists are also evident in the molecule, in particular about the N(a)–C(b) (a = amine and b = benzene) bond [C—N—C—C = −144.79 (18)°]. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds result in the formation of eight-membered {⋯NCNH}(2) synthons [or R (2) (2)(8) loops]. |
format | Text |
id | pubmed-3007248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30072482010-12-30 N-(4-Chlorophenyl)-4-methylpyridin-2-amine Fairuz, Zainal A. Aiyub, Zaharah Abdullah, Zanariah Ng, Seik Weng Tiekink, Edward R. T. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(11)ClN(2), the dihedral angle between the benzene and pyridyl rings is 48.03 (8)°. Twists are also evident in the molecule, in particular about the N(a)–C(b) (a = amine and b = benzene) bond [C—N—C—C = −144.79 (18)°]. In the crystal, inversion dimers linked by pairs of N—H⋯N hydrogen bonds result in the formation of eight-membered {⋯NCNH}(2) synthons [or R (2) (2)(8) loops]. International Union of Crystallography 2010-07-31 /pmc/articles/PMC3007248/ /pubmed/21588463 http://dx.doi.org/10.1107/S1600536810030138 Text en © Fairuz 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 Fairuz, Zainal A. Aiyub, Zaharah Abdullah, Zanariah Ng, Seik Weng Tiekink, Edward R. T. N-(4-Chlorophenyl)-4-methylpyridin-2-amine |
title |
N-(4-Chlorophenyl)-4-methylpyridin-2-amine |
title_full |
N-(4-Chlorophenyl)-4-methylpyridin-2-amine |
title_fullStr |
N-(4-Chlorophenyl)-4-methylpyridin-2-amine |
title_full_unstemmed |
N-(4-Chlorophenyl)-4-methylpyridin-2-amine |
title_short |
N-(4-Chlorophenyl)-4-methylpyridin-2-amine |
title_sort | n-(4-chlorophenyl)-4-methylpyridin-2-amine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007248/ https://www.ncbi.nlm.nih.gov/pubmed/21588463 http://dx.doi.org/10.1107/S1600536810030138 |
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