Cargando…

(Z)-3-(Benzyl­carbamo­yl)prop-2-enoic acid

The title compound, C(11)H(11)NO(3), was synthesized by the reaction of maleic andydride and phenyl­methanamine. The mol­ecular conformation is stabilized by by an intra­molecular O—H⋯O hydrogen bond. In the crystal, mol­ecules are linked by inter­molecular N—H⋯O and C—H⋯O hydrogen bonds, forming a...

Descripción completa

Detalles Bibliográficos
Autores principales: Dong, Su-Lan, Cheng, Xiao-Chun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052078/
https://www.ncbi.nlm.nih.gov/pubmed/21522434
http://dx.doi.org/10.1107/S160053681100609X
_version_ 1782199622070960128
author Dong, Su-Lan
Cheng, Xiao-Chun
author_facet Dong, Su-Lan
Cheng, Xiao-Chun
author_sort Dong, Su-Lan
collection PubMed
description The title compound, C(11)H(11)NO(3), was synthesized by the reaction of maleic andydride and phenyl­methanamine. The mol­ecular conformation is stabilized by by an intra­molecular O—H⋯O hydrogen bond. In the crystal, mol­ecules are linked by inter­molecular N—H⋯O and C—H⋯O hydrogen bonds, forming a chain along the b axis.
format Text
id pubmed-3052078
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30520782011-04-26 (Z)-3-(Benzyl­carbamo­yl)prop-2-enoic acid Dong, Su-Lan Cheng, Xiao-Chun Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(11)H(11)NO(3), was synthesized by the reaction of maleic andydride and phenyl­methanamine. The mol­ecular conformation is stabilized by by an intra­molecular O—H⋯O hydrogen bond. In the crystal, mol­ecules are linked by inter­molecular N—H⋯O and C—H⋯O hydrogen bonds, forming a chain along the b axis. International Union of Crystallography 2011-02-23 /pmc/articles/PMC3052078/ /pubmed/21522434 http://dx.doi.org/10.1107/S160053681100609X Text en © Dong and Cheng 2011 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
Dong, Su-Lan
Cheng, Xiao-Chun
(Z)-3-(Benzyl­carbamo­yl)prop-2-enoic acid
title (Z)-3-(Benzyl­carbamo­yl)prop-2-enoic acid
title_full (Z)-3-(Benzyl­carbamo­yl)prop-2-enoic acid
title_fullStr (Z)-3-(Benzyl­carbamo­yl)prop-2-enoic acid
title_full_unstemmed (Z)-3-(Benzyl­carbamo­yl)prop-2-enoic acid
title_short (Z)-3-(Benzyl­carbamo­yl)prop-2-enoic acid
title_sort (z)-3-(benzyl­carbamo­yl)prop-2-enoic acid
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052078/
https://www.ncbi.nlm.nih.gov/pubmed/21522434
http://dx.doi.org/10.1107/S160053681100609X
work_keys_str_mv AT dongsulan z3benzylcarbamoylprop2enoicacid
AT chengxiaochun z3benzylcarbamoylprop2enoicacid