[2-(1,3-Benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone

In the title compound, C(21)H(13)BrClNO(2)S, the dihedral angle between the planes of the benzothia­zole and chloro­phenyl­methanone groups is 71.34 (6)°. In the crystal, weak C—H⋯N hydrogen bonds lead to dimer formation, whereas Br⋯Cl short contacts [3.4966 (11) Å] form infinite chains along the a-...

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Detalles Bibliográficos
Autores principales: Nayak, Susanta K., Venugopala, K. N., Govender, Thavendran, Kruger, Hendrik G., Maguire, Glenn E. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588233/
https://www.ncbi.nlm.nih.gov/pubmed/23476451
http://dx.doi.org/10.1107/S1600536812049756
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author Nayak, Susanta K.
Venugopala, K. N.
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
author_facet Nayak, Susanta K.
Venugopala, K. N.
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
author_sort Nayak, Susanta K.
collection PubMed
description In the title compound, C(21)H(13)BrClNO(2)S, the dihedral angle between the planes of the benzothia­zole and chloro­phenyl­methanone groups is 71.34 (6)°. In the crystal, weak C—H⋯N hydrogen bonds lead to dimer formation, whereas Br⋯Cl short contacts [3.4966 (11) Å] form infinite chains along the a-axis direction. Further, the C—H⋯O, C—H⋯π and π–π [centroid–centroid distance = 3.865 (2) Å] inter­actions stabilize the three-dimensional network.
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spelling pubmed-35882332013-03-08 [2-(1,3-Benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone Nayak, Susanta K. Venugopala, K. N. Govender, Thavendran Kruger, Hendrik G. Maguire, Glenn E. M. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(21)H(13)BrClNO(2)S, the dihedral angle between the planes of the benzothia­zole and chloro­phenyl­methanone groups is 71.34 (6)°. In the crystal, weak C—H⋯N hydrogen bonds lead to dimer formation, whereas Br⋯Cl short contacts [3.4966 (11) Å] form infinite chains along the a-axis direction. Further, the C—H⋯O, C—H⋯π and π–π [centroid–centroid distance = 3.865 (2) Å] inter­actions stabilize the three-dimensional network. International Union of Crystallography 2012-12-12 /pmc/articles/PMC3588233/ /pubmed/23476451 http://dx.doi.org/10.1107/S1600536812049756 Text en © Nayak et al. 2013 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
Nayak, Susanta K.
Venugopala, K. N.
Govender, Thavendran
Kruger, Hendrik G.
Maguire, Glenn E. M.
[2-(1,3-Benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone
title [2-(1,3-Benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone
title_full [2-(1,3-Benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone
title_fullStr [2-(1,3-Benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone
title_full_unstemmed [2-(1,3-Benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone
title_short [2-(1,3-Benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone
title_sort [2-(1,3-benzothia­zol-2-ylmeth­oxy)-5-bromo­phen­yl](4-chloro­phen­yl)methanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588233/
https://www.ncbi.nlm.nih.gov/pubmed/23476451
http://dx.doi.org/10.1107/S1600536812049756
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