Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl­ate

In the title compound, C(9)H(13)NO(2), there are two independent mol­ecules per asymmetric unit. The mol­ecules are very similar and almost planar, with the ethoxy­carbonyl group anti to the pyrrole N atom. The two independent mol­ecules are joined into dimeric units by strong hydrogen bonds between...

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Detalles Bibliográficos
Autores principales: Arranja, Cláudia T., Ramos Silva, Manuela, Matos Beja, Ana, Ferreira, Ana F. P. V., Sobral, Abílio J. F. N.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959273/
https://www.ncbi.nlm.nih.gov/pubmed/21201188
http://dx.doi.org/10.1107/S1600536808029929
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author Arranja, Cláudia T.
Ramos Silva, Manuela
Matos Beja, Ana
Ferreira, Ana F. P. V.
Sobral, Abílio J. F. N.
author_facet Arranja, Cláudia T.
Ramos Silva, Manuela
Matos Beja, Ana
Ferreira, Ana F. P. V.
Sobral, Abílio J. F. N.
author_sort Arranja, Cláudia T.
collection PubMed
description In the title compound, C(9)H(13)NO(2), there are two independent mol­ecules per asymmetric unit. The mol­ecules are very similar and almost planar, with the ethoxy­carbonyl group anti to the pyrrole N atom. The two independent mol­ecules are joined into dimeric units by strong hydrogen bonds between NH groups and carbonyl O atoms.
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spelling pubmed-29592732010-12-30 Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl­ate Arranja, Cláudia T. Ramos Silva, Manuela Matos Beja, Ana Ferreira, Ana F. P. V. Sobral, Abílio J. F. N. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(9)H(13)NO(2), there are two independent mol­ecules per asymmetric unit. The mol­ecules are very similar and almost planar, with the ethoxy­carbonyl group anti to the pyrrole N atom. The two independent mol­ecules are joined into dimeric units by strong hydrogen bonds between NH groups and carbonyl O atoms. International Union of Crystallography 2008-09-24 /pmc/articles/PMC2959273/ /pubmed/21201188 http://dx.doi.org/10.1107/S1600536808029929 Text en © Arranja et al. 2008 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
Arranja, Cláudia T.
Ramos Silva, Manuela
Matos Beja, Ana
Ferreira, Ana F. P. V.
Sobral, Abílio J. F. N.
Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl­ate
title Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl­ate
title_full Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl­ate
title_fullStr Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl­ate
title_full_unstemmed Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl­ate
title_short Ethyl 3,5-dimethyl-1H-pyrrole-2-carboxyl­ate
title_sort ethyl 3,5-dimethyl-1h-pyrrole-2-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959273/
https://www.ncbi.nlm.nih.gov/pubmed/21201188
http://dx.doi.org/10.1107/S1600536808029929
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AT sobralabiliojfn ethyl35dimethyl1hpyrrole2carboxylate

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