1-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone

1-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone

The title compound, C19H18Cl2N2O5, was synthesized by the reaction of N′-(3,4-dichlorobenzylidene)-3,4,5-trimethoxybenzohydrazide and acetic anhydride. The oxadiazole ring makes dihedral angles of 82.82 (7) and 9.92 (7)° with the 3,4-dichlorobenzene and the 3,4...

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Main Authors: Dao-Hang He, Yong-Chuang Zhu
Format: Article
Language:English
Published: International Union of Crystallography 2008-08-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536808020771
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spelling doaj-3250092a14be4395abf3539d39e69db12020-11-25T00:50:21ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682008-08-01648o1443o144310.1107/S16005368080207711-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanoneDao-Hang HeYong-Chuang ZhuThe title compound, C19H18Cl2N2O5, was synthesized by the reaction of N′-(3,4-dichlorobenzylidene)-3,4,5-trimethoxybenzohydrazide and acetic anhydride. The oxadiazole ring makes dihedral angles of 82.82 (7) and 9.92 (7)° with the 3,4-dichlorobenzene and the 3,4,5-trimethoxybenzene ring planes, respectively. The crystal structure is stabilized by intermolecular C—H... O and C—H... N hydrogen bonds. Intramolecular C—H...O and C—H...N hydrogen bonds are also present.http://scripts.iucr.org/cgi-bin/paper?S1600536808020771
collection DOAJ
language English
format Article
sources DOAJ
author Dao-Hang He
Yong-Chuang Zhu
spellingShingle Dao-Hang He
Yong-Chuang Zhu
1-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone
Acta Crystallographica Section E
author_facet Dao-Hang He
Yong-Chuang Zhu
author_sort Dao-Hang He
title 1-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone
title_short 1-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone
title_full 1-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone
title_fullStr 1-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone
title_full_unstemmed 1-[2-(3,4-Dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone
title_sort 1-[2-(3,4-dichlorophenyl)-5-(3,4,5-trimethoxyphenyl)-2,3-dihydro-1,3,4-oxadiazol-3-yl]ethanone
publisher International Union of Crystallography
series Acta Crystallographica Section E
issn 1600-5368
publishDate 2008-08-01
description The title compound, C19H18Cl2N2O5, was synthesized by the reaction of N′-(3,4-dichlorobenzylidene)-3,4,5-trimethoxybenzohydrazide and acetic anhydride. The oxadiazole ring makes dihedral angles of 82.82 (7) and 9.92 (7)° with the 3,4-dichlorobenzene and the 3,4,5-trimethoxybenzene ring planes, respectively. The crystal structure is stabilized by intermolecular C—H... O and C—H... N hydrogen bonds. Intramolecular C—H...O and C—H...N hydrogen bonds are also present.
url http://scripts.iucr.org/cgi-bin/paper?S1600536808020771
work_keys_str_mv AT daohanghe 1234dichlorophenyl5345trimethoxyphenyl23dihydro134oxadiazol3ylethanone
AT yongchuangzhu 1234dichlorophenyl5345trimethoxyphenyl23dihydro134oxadiazol3ylethanone
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