2,5-Dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate

In the title compound, C(8)H(9)NO(4), the pyrrolidine ring (r.m.s. deviation 0.014 Å) is almost normal to the mean plane of the propenoate group (r.m.s deviation 0.028 Å), making a dihedral angle of 86.58 (4)°. In the crystal, mol­ecules are linked via pairs of weak C—H⋯O hydrogen bonds, forming inv...

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Detalles Bibliográficos
Autores principales: Pearson, Wayne H., Lin, Shirley, Isaacs, Lyle
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998608/
https://www.ncbi.nlm.nih.gov/pubmed/24826149
http://dx.doi.org/10.1107/S1600536814005170
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author Pearson, Wayne H.
Lin, Shirley
Isaacs, Lyle
author_facet Pearson, Wayne H.
Lin, Shirley
Isaacs, Lyle
author_sort Pearson, Wayne H.
collection PubMed
description In the title compound, C(8)H(9)NO(4), the pyrrolidine ring (r.m.s. deviation 0.014 Å) is almost normal to the mean plane of the propenoate group (r.m.s deviation 0.028 Å), making a dihedral angle of 86.58 (4)°. In the crystal, mol­ecules are linked via pairs of weak C—H⋯O hydrogen bonds, forming inversion dimers which stack along the c axis.
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spelling pubmed-39986082014-05-13 2,5-Dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate Pearson, Wayne H. Lin, Shirley Isaacs, Lyle Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(8)H(9)NO(4), the pyrrolidine ring (r.m.s. deviation 0.014 Å) is almost normal to the mean plane of the propenoate group (r.m.s deviation 0.028 Å), making a dihedral angle of 86.58 (4)°. In the crystal, mol­ecules are linked via pairs of weak C—H⋯O hydrogen bonds, forming inversion dimers which stack along the c axis. International Union of Crystallography 2014-03-15 /pmc/articles/PMC3998608/ /pubmed/24826149 http://dx.doi.org/10.1107/S1600536814005170 Text en © Pearson et al. 2014 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
Pearson, Wayne H.
Lin, Shirley
Isaacs, Lyle
2,5-Dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate
title 2,5-Dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate
title_full 2,5-Dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate
title_fullStr 2,5-Dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate
title_full_unstemmed 2,5-Dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate
title_short 2,5-Dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate
title_sort 2,5-dioxopyrrolidin-1-yl 2-methyl­prop-2-enoate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3998608/
https://www.ncbi.nlm.nih.gov/pubmed/24826149
http://dx.doi.org/10.1107/S1600536814005170
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