3-[(3,5-Dichloroanilino)carbonyl]propionic acid

In the crystal structure of the title compound, C10H9Cl2NO3, the conformations of the amide O atom and the carbonyl O atom of the acid segment are anti to the H atoms of the adjacent –CH2 groups. The C=O and O—H bonds of the acid group are in relatively rare anti position...

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Main Authors: B. Thimme Gowda, Sabine Foro, B. S. Saraswathi, Hiromitsu Terao, Hartmut Fuess
Format: Article
Language:English
Published: International Union of Crystallography 2009-04-01
Series:Acta Crystallographica Section E
Online Access:http://scripts.iucr.org/cgi-bin/paper?S1600536809010319
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author B. Thimme Gowda
Sabine Foro
B. S. Saraswathi
Hiromitsu Terao
Hartmut Fuess
author_facet B. Thimme Gowda
Sabine Foro
B. S. Saraswathi
Hiromitsu Terao
Hartmut Fuess
author_sort B. Thimme Gowda
collection DOAJ
description In the crystal structure of the title compound, C10H9Cl2NO3, the conformations of the amide O atom and the carbonyl O atom of the acid segment are anti to the H atoms of the adjacent –CH2 groups. The C=O and O—H bonds of the acid group are in relatively rare anti positions with respect to each other. This is an obvious consequence of the concerted effects of both the all-anti molecular conformation and the intermolecular hydrogen bond donated to the amide carbonyl group. In the crystal, molecules are packed into infinite chains through intermolecular N—H...O and O—H...O hydrogen bonds.
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spelling doaj.art-398b782a230640929e8bacea5b45d3152022-12-21T21:10:17ZengInternational Union of CrystallographyActa Crystallographica Section E1600-53682009-04-01654o873o87310.1107/S16005368090103193-[(3,5-Dichloroanilino)carbonyl]propionic acidB. Thimme GowdaSabine ForoB. S. SaraswathiHiromitsu TeraoHartmut FuessIn the crystal structure of the title compound, C10H9Cl2NO3, the conformations of the amide O atom and the carbonyl O atom of the acid segment are anti to the H atoms of the adjacent –CH2 groups. The C=O and O—H bonds of the acid group are in relatively rare anti positions with respect to each other. This is an obvious consequence of the concerted effects of both the all-anti molecular conformation and the intermolecular hydrogen bond donated to the amide carbonyl group. In the crystal, molecules are packed into infinite chains through intermolecular N—H...O and O—H...O hydrogen bonds.http://scripts.iucr.org/cgi-bin/paper?S1600536809010319
spellingShingle B. Thimme Gowda
Sabine Foro
B. S. Saraswathi
Hiromitsu Terao
Hartmut Fuess
3-[(3,5-Dichloroanilino)carbonyl]propionic acid
Acta Crystallographica Section E
title 3-[(3,5-Dichloroanilino)carbonyl]propionic acid
title_full 3-[(3,5-Dichloroanilino)carbonyl]propionic acid
title_fullStr 3-[(3,5-Dichloroanilino)carbonyl]propionic acid
title_full_unstemmed 3-[(3,5-Dichloroanilino)carbonyl]propionic acid
title_short 3-[(3,5-Dichloroanilino)carbonyl]propionic acid
title_sort 3 3 5 dichloroanilino carbonyl propionic acid
url http://scripts.iucr.org/cgi-bin/paper?S1600536809010319
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AT sabineforo 335dichloroanilinocarbonylpropionicacid
AT bssaraswathi 335dichloroanilinocarbonylpropionicacid
AT hiromitsuterao 335dichloroanilinocarbonylpropionicacid
AT hartmutfuess 335dichloroanilinocarbonylpropionicacid