N-(4-Chlorobutanoyl)-N′-(2,5-dimethoxyphenyl)thiourea
The title molecule, C13H17ClN2O3S, shows an anti and syn disposition of the butanoyl and 2,5-dimethoxyphenyl groups with respect to the thione and is stabilized by intramolecular N—H...O and weak C—H...S hydrogen bonds. In the crystal, intermolecular N—H...S...
Main Authors: | , , |
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Format: | Article |
Language: | English |
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International Union of Crystallography
2011-10-01
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Series: | Acta Crystallographica Section E |
Online Access: | http://scripts.iucr.org/cgi-bin/paper?S1600536811036002 |
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author | Bohari M. Yamin Norafiqah R. Azmi M. Sukeri M. Yusof |
author_facet | Bohari M. Yamin Norafiqah R. Azmi M. Sukeri M. Yusof |
author_sort | Bohari M. Yamin |
collection | DOAJ |
description | The title molecule, C13H17ClN2O3S, shows an anti and syn disposition of the butanoyl and 2,5-dimethoxyphenyl groups with respect to the thione and is stabilized by intramolecular N—H...O and weak C—H...S hydrogen bonds. In the crystal, intermolecular N—H...S hydrogen bonds link the molecules into centrosymmetric dimers. The crystal structure is stabilized by weak C—H...O and C—H...S contacts. |
first_indexed | 2024-12-24T19:12:45Z |
format | Article |
id | doaj.art-9cc02d5b358c44598f0c948c9fd77aab |
institution | Directory Open Access Journal |
issn | 1600-5368 |
language | English |
last_indexed | 2024-12-24T19:12:45Z |
publishDate | 2011-10-01 |
publisher | International Union of Crystallography |
record_format | Article |
series | Acta Crystallographica Section E |
spelling | doaj.art-9cc02d5b358c44598f0c948c9fd77aab2022-12-21T16:42:58ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682011-10-016710o2609o260910.1107/S1600536811036002N-(4-Chlorobutanoyl)-N′-(2,5-dimethoxyphenyl)thioureaBohari M. YaminNorafiqah R. AzmiM. Sukeri M. YusofThe title molecule, C13H17ClN2O3S, shows an anti and syn disposition of the butanoyl and 2,5-dimethoxyphenyl groups with respect to the thione and is stabilized by intramolecular N—H...O and weak C—H...S hydrogen bonds. In the crystal, intermolecular N—H...S hydrogen bonds link the molecules into centrosymmetric dimers. The crystal structure is stabilized by weak C—H...O and C—H...S contacts.http://scripts.iucr.org/cgi-bin/paper?S1600536811036002 |
spellingShingle | Bohari M. Yamin Norafiqah R. Azmi M. Sukeri M. Yusof N-(4-Chlorobutanoyl)-N′-(2,5-dimethoxyphenyl)thiourea Acta Crystallographica Section E |
title | N-(4-Chlorobutanoyl)-N′-(2,5-dimethoxyphenyl)thiourea |
title_full | N-(4-Chlorobutanoyl)-N′-(2,5-dimethoxyphenyl)thiourea |
title_fullStr | N-(4-Chlorobutanoyl)-N′-(2,5-dimethoxyphenyl)thiourea |
title_full_unstemmed | N-(4-Chlorobutanoyl)-N′-(2,5-dimethoxyphenyl)thiourea |
title_short | N-(4-Chlorobutanoyl)-N′-(2,5-dimethoxyphenyl)thiourea |
title_sort | n 4 chlorobutanoyl n amp 8242 2 5 dimethoxyphenyl thiourea |
url | http://scripts.iucr.org/cgi-bin/paper?S1600536811036002 |
work_keys_str_mv | AT boharimyamin n4chlorobutanoylnamp824225dimethoxyphenylthiourea AT norafiqahrazmi n4chlorobutanoylnamp824225dimethoxyphenylthiourea AT msukerimyusof n4chlorobutanoylnamp824225dimethoxyphenylthiourea |