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1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea
The title compound, C(15)H(10)ClF(3)N(2)O(3), is considered to belong to a fourth generation of insecticides with properties such as high selectivity, low acute toxicity for mammals and high biological activity. The dihedral angle between the two benzene rings is 59.3 (2)°. Intramolecular C—H⋯O and...
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/PMC2961706/ https://www.ncbi.nlm.nih.gov/pubmed/21202855 http://dx.doi.org/10.1107/S1600536808016462 |
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author | Liu, Yin-hong Li, Fang-shi Yin, Li-he Yu, Da-sheng |
author_facet | Liu, Yin-hong Li, Fang-shi Yin, Li-he Yu, Da-sheng |
author_sort | Liu, Yin-hong |
collection | PubMed |
description | The title compound, C(15)H(10)ClF(3)N(2)O(3), is considered to belong to a fourth generation of insecticides with properties such as high selectivity, low acute toxicity for mammals and high biological activity. The dihedral angle between the two benzene rings is 59.3 (2)°. Intramolecular C—H⋯O and N—H⋯O hydrogen bonds are observed. Intermolecular N—H⋯O hydrogen bonding generates a centrosymmetric dimer. The F atoms are disordered over two positions; the site occupancy factors are 0.52 and 0.48. |
format | Text |
id | pubmed-2961706 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29617062010-12-30 1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea Liu, Yin-hong Li, Fang-shi Yin, Li-he Yu, Da-sheng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(15)H(10)ClF(3)N(2)O(3), is considered to belong to a fourth generation of insecticides with properties such as high selectivity, low acute toxicity for mammals and high biological activity. The dihedral angle between the two benzene rings is 59.3 (2)°. Intramolecular C—H⋯O and N—H⋯O hydrogen bonds are observed. Intermolecular N—H⋯O hydrogen bonding generates a centrosymmetric dimer. The F atoms are disordered over two positions; the site occupancy factors are 0.52 and 0.48. International Union of Crystallography 2008-06-07 /pmc/articles/PMC2961706/ /pubmed/21202855 http://dx.doi.org/10.1107/S1600536808016462 Text en © Liu 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 Liu, Yin-hong Li, Fang-shi Yin, Li-he Yu, Da-sheng 1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea |
title | 1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea |
title_full | 1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea |
title_fullStr | 1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea |
title_full_unstemmed | 1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea |
title_short | 1-(2-Chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea |
title_sort | 1-(2-chlorobenzoyl)-3-[4-(trifluoromethoxy)phenyl]urea |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961706/ https://www.ncbi.nlm.nih.gov/pubmed/21202855 http://dx.doi.org/10.1107/S1600536808016462 |
work_keys_str_mv | AT liuyinhong 12chlorobenzoyl34trifluoromethoxyphenylurea AT lifangshi 12chlorobenzoyl34trifluoromethoxyphenylurea AT yinlihe 12chlorobenzoyl34trifluoromethoxyphenylurea AT yudasheng 12chlorobenzoyl34trifluoromethoxyphenylurea |