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5-(3-Fluorophenyl)-1,3,4-thiadiazol-2-amine
The title compound, C(8)H(6)FN(3)S, was synthesized by the reaction of 3-fluorobenzoic acid and thiosemicarbazide. The dihedral angle between the planes of the thiadiazole and benzene rings is 37.3 (2)°. In the structure, two crystallographically independent molecules form a centrosymmetric dime...
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969772/ https://www.ncbi.nlm.nih.gov/pubmed/21583266 http://dx.doi.org/10.1107/S1600536809019333 |
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author | Wang, Yao Wan, Rong Han, Feng Wang, Peng |
author_facet | Wang, Yao Wan, Rong Han, Feng Wang, Peng |
author_sort | Wang, Yao |
collection | PubMed |
description | The title compound, C(8)H(6)FN(3)S, was synthesized by the reaction of 3-fluorobenzoic acid and thiosemicarbazide. The dihedral angle between the planes of the thiadiazole and benzene rings is 37.3 (2)°. In the structure, two crystallographically independent molecules form a centrosymmetric dimer, in which two intermolecular N—H⋯N hydrogen bonds generate an R (2) (2)(8) motif. |
format | Text |
id | pubmed-2969772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29697722010-12-30 5-(3-Fluorophenyl)-1,3,4-thiadiazol-2-amine Wang, Yao Wan, Rong Han, Feng Wang, Peng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(8)H(6)FN(3)S, was synthesized by the reaction of 3-fluorobenzoic acid and thiosemicarbazide. The dihedral angle between the planes of the thiadiazole and benzene rings is 37.3 (2)°. In the structure, two crystallographically independent molecules form a centrosymmetric dimer, in which two intermolecular N—H⋯N hydrogen bonds generate an R (2) (2)(8) motif. International Union of Crystallography 2009-05-29 /pmc/articles/PMC2969772/ /pubmed/21583266 http://dx.doi.org/10.1107/S1600536809019333 Text en © Wang et al. 2009 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 Wang, Yao Wan, Rong Han, Feng Wang, Peng 5-(3-Fluorophenyl)-1,3,4-thiadiazol-2-amine |
title | 5-(3-Fluorophenyl)-1,3,4-thiadiazol-2-amine |
title_full | 5-(3-Fluorophenyl)-1,3,4-thiadiazol-2-amine |
title_fullStr | 5-(3-Fluorophenyl)-1,3,4-thiadiazol-2-amine |
title_full_unstemmed | 5-(3-Fluorophenyl)-1,3,4-thiadiazol-2-amine |
title_short | 5-(3-Fluorophenyl)-1,3,4-thiadiazol-2-amine |
title_sort | 5-(3-fluorophenyl)-1,3,4-thiadiazol-2-amine |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969772/ https://www.ncbi.nlm.nih.gov/pubmed/21583266 http://dx.doi.org/10.1107/S1600536809019333 |
work_keys_str_mv | AT wangyao 53fluorophenyl134thiadiazol2amine AT wanrong 53fluorophenyl134thiadiazol2amine AT hanfeng 53fluorophenyl134thiadiazol2amine AT wangpeng 53fluorophenyl134thiadiazol2amine |