Methyl N-(4-chlorophenyl)succinamate

In the structure of the title compound {systematic name: methyl 3-[(4-chloro­phen­yl)amino­carbon­yl]propionate}, C(11)H(12)ClNO(3), the conformations of the N—H and C=O bonds in the amide fragment are trans to each other and the conformations of the amide O atom and the carbonyl O atom of the ester...

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Autores principales: Gowda, B. Thimme, Foro, Sabine, Saraswathi, B. S., Terao, Hiromitsu, Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968232/
https://www.ncbi.nlm.nih.gov/pubmed/21581983
http://dx.doi.org/10.1107/S1600536809002724
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author Gowda, B. Thimme
Foro, Sabine
Saraswathi, B. S.
Terao, Hiromitsu
Fuess, Hartmut
author_facet Gowda, B. Thimme
Foro, Sabine
Saraswathi, B. S.
Terao, Hiromitsu
Fuess, Hartmut
author_sort Gowda, B. Thimme
collection PubMed
description In the structure of the title compound {systematic name: methyl 3-[(4-chloro­phen­yl)amino­carbon­yl]propionate}, C(11)H(12)ClNO(3), the conformations of the N—H and C=O bonds in the amide fragment are trans to each other and the conformations of the amide O atom and the carbonyl O atom of the ester fragment are also trans to the H atoms attached to the adjacent C atoms. Mol­ecules are linked into a centrosymmetric R (2) (2)(14) dimer by simple N—H⋯O inter­actions. Furthermore, a short intra­molecular C—H⋯O contact may stabilize the conformation adopted by the mol­ecule in the crystal.
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spelling pubmed-29682322010-12-30 Methyl N-(4-chlorophenyl)succinamate Gowda, B. Thimme Foro, Sabine Saraswathi, B. S. Terao, Hiromitsu Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the structure of the title compound {systematic name: methyl 3-[(4-chloro­phen­yl)amino­carbon­yl]propionate}, C(11)H(12)ClNO(3), the conformations of the N—H and C=O bonds in the amide fragment are trans to each other and the conformations of the amide O atom and the carbonyl O atom of the ester fragment are also trans to the H atoms attached to the adjacent C atoms. Mol­ecules are linked into a centrosymmetric R (2) (2)(14) dimer by simple N—H⋯O inter­actions. Furthermore, a short intra­molecular C—H⋯O contact may stabilize the conformation adopted by the mol­ecule in the crystal. International Union of Crystallography 2009-01-28 /pmc/articles/PMC2968232/ /pubmed/21581983 http://dx.doi.org/10.1107/S1600536809002724 Text en © Gowda et al. 2009 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
Gowda, B. Thimme
Foro, Sabine
Saraswathi, B. S.
Terao, Hiromitsu
Fuess, Hartmut
Methyl N-(4-chlorophenyl)succinamate
title Methyl N-(4-chlorophenyl)succinamate
title_full Methyl N-(4-chlorophenyl)succinamate
title_fullStr Methyl N-(4-chlorophenyl)succinamate
title_full_unstemmed Methyl N-(4-chlorophenyl)succinamate
title_short Methyl N-(4-chlorophenyl)succinamate
title_sort methyl n-(4-chlorophenyl)succinamate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2968232/
https://www.ncbi.nlm.nih.gov/pubmed/21581983
http://dx.doi.org/10.1107/S1600536809002724
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