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Methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate

In the title compound, C(11)H(11)Cl(2)NO(3), the amide O atom and the carbonyl O atom of the ester segment are anti to each other and anti to the H atoms of the adjacent –CH(2) groups. In the crystal structure, mol­ecules are packed into centrosymmetric dimers through inter­molecular N—H⋯O hydrogen...

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Detalles Bibliográficos
Autores principales: Saraswathi, B. S., Gowda, B. Thimme, Foro, Sabine, Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979985/
https://www.ncbi.nlm.nih.gov/pubmed/21579808
http://dx.doi.org/10.1107/S1600536810001455
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author Saraswathi, B. S.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
author_facet Saraswathi, B. S.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
author_sort Saraswathi, B. S.
collection PubMed
description In the title compound, C(11)H(11)Cl(2)NO(3), the amide O atom and the carbonyl O atom of the ester segment are anti to each other and anti to the H atoms of the adjacent –CH(2) groups. In the crystal structure, mol­ecules are packed into centrosymmetric dimers through inter­molecular N—H⋯O hydrogen bonds. The dimers are linked into a layer structure extending parallel to ([Image: see text]02) by C—H⋯O hydrogen bonds.
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spelling pubmed-29799852010-12-30 Methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate Saraswathi, B. S. Gowda, B. Thimme Foro, Sabine Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(11)Cl(2)NO(3), the amide O atom and the carbonyl O atom of the ester segment are anti to each other and anti to the H atoms of the adjacent –CH(2) groups. In the crystal structure, mol­ecules are packed into centrosymmetric dimers through inter­molecular N—H⋯O hydrogen bonds. The dimers are linked into a layer structure extending parallel to ([Image: see text]02) by C—H⋯O hydrogen bonds. International Union of Crystallography 2010-01-16 /pmc/articles/PMC2979985/ /pubmed/21579808 http://dx.doi.org/10.1107/S1600536810001455 Text en © Saraswathi et al. 2010 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
Saraswathi, B. S.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
Methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate
title Methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate
title_full Methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate
title_fullStr Methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate
title_full_unstemmed Methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate
title_short Methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate
title_sort methyl 3-[(3,5-dichloro­anilino)carbon­yl]propionate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979985/
https://www.ncbi.nlm.nih.gov/pubmed/21579808
http://dx.doi.org/10.1107/S1600536810001455
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