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2,2,2-Trichloro-N-(2,5-dimethylphenyl)acetamide
The N—H bond in the title compound, C(10)H(10)Cl(3)NO, is syn to the 2-methyl and anti to the 5-methyl substituent of the aromatic ring. Adjacent molecules are linked into chains through N—H⋯O hydrogen bonding. Two Cl atoms are each disordered equally over two sites.
Autores principales: | , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961108/ https://www.ncbi.nlm.nih.gov/pubmed/21202317 http://dx.doi.org/10.1107/S1600536808009264 |
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author | Gowda, B. Thimme Foro, Sabine Fuess, Hartmut |
author_facet | Gowda, B. Thimme Foro, Sabine Fuess, Hartmut |
author_sort | Gowda, B. Thimme |
collection | PubMed |
description | The N—H bond in the title compound, C(10)H(10)Cl(3)NO, is syn to the 2-methyl and anti to the 5-methyl substituent of the aromatic ring. Adjacent molecules are linked into chains through N—H⋯O hydrogen bonding. Two Cl atoms are each disordered equally over two sites. |
format | Text |
id | pubmed-2961108 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29611082010-12-30 2,2,2-Trichloro-N-(2,5-dimethylphenyl)acetamide Gowda, B. Thimme Foro, Sabine Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The N—H bond in the title compound, C(10)H(10)Cl(3)NO, is syn to the 2-methyl and anti to the 5-methyl substituent of the aromatic ring. Adjacent molecules are linked into chains through N—H⋯O hydrogen bonding. Two Cl atoms are each disordered equally over two sites. International Union of Crystallography 2008-04-10 /pmc/articles/PMC2961108/ /pubmed/21202317 http://dx.doi.org/10.1107/S1600536808009264 Text en © Gowda et al. 2008 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 Gowda, B. Thimme Foro, Sabine Fuess, Hartmut 2,2,2-Trichloro-N-(2,5-dimethylphenyl)acetamide |
title | 2,2,2-Trichloro-N-(2,5-dimethylphenyl)acetamide |
title_full | 2,2,2-Trichloro-N-(2,5-dimethylphenyl)acetamide |
title_fullStr | 2,2,2-Trichloro-N-(2,5-dimethylphenyl)acetamide |
title_full_unstemmed | 2,2,2-Trichloro-N-(2,5-dimethylphenyl)acetamide |
title_short | 2,2,2-Trichloro-N-(2,5-dimethylphenyl)acetamide |
title_sort | 2,2,2-trichloro-n-(2,5-dimethylphenyl)acetamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961108/ https://www.ncbi.nlm.nih.gov/pubmed/21202317 http://dx.doi.org/10.1107/S1600536808009264 |
work_keys_str_mv | AT gowdabthimme 222trichloron25dimethylphenylacetamide AT forosabine 222trichloron25dimethylphenylacetamide AT fuesshartmut 222trichloron25dimethylphenylacetamide |