Cytenamide–butyric acid (1/1)

Cytenamide forms a 1:1 solvate with butyric acid [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–butanoic acid (1/1)], C(16)H(13)NO·C(4)H(8)O(2). The title compound crystallizes with one mol­ecule of cytenamide and one of butyric acid in the asymmetric unit; these mol­ecules are li...

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Detalles Bibliográficos
Autores principales: Johnston, Andrea, Florence, Alastair J., Fabbiani, Francesca J. A., Shankland, Kenneth, Bedford, Colin T.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961685/
https://www.ncbi.nlm.nih.gov/pubmed/21202925
http://dx.doi.org/10.1107/S1600536808018059
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author Johnston, Andrea
Florence, Alastair J.
Fabbiani, Francesca J. A.
Shankland, Kenneth
Bedford, Colin T.
author_facet Johnston, Andrea
Florence, Alastair J.
Fabbiani, Francesca J. A.
Shankland, Kenneth
Bedford, Colin T.
author_sort Johnston, Andrea
collection PubMed
description Cytenamide forms a 1:1 solvate with butyric acid [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–butanoic acid (1/1)], C(16)H(13)NO·C(4)H(8)O(2). The title compound crystallizes with one mol­ecule of cytenamide and one of butyric acid in the asymmetric unit; these mol­ecules are linked by N—H⋯O and O—H⋯O hydrogen bonds to form an R (2) (2)(8) heterodimer motif. Pairs of adjacent motifs are further connected via N—H⋯O inter­actions to form a discrete centrosymmetric assembly.
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spelling pubmed-29616852010-12-30 Cytenamide–butyric acid (1/1) Johnston, Andrea Florence, Alastair J. Fabbiani, Francesca J. A. Shankland, Kenneth Bedford, Colin T. Acta Crystallogr Sect E Struct Rep Online Organic Papers Cytenamide forms a 1:1 solvate with butyric acid [systematic name: 5H-dibenzo[a,d]cyclo­hepta­triene-5-carboxamide–butanoic acid (1/1)], C(16)H(13)NO·C(4)H(8)O(2). The title compound crystallizes with one mol­ecule of cytenamide and one of butyric acid in the asymmetric unit; these mol­ecules are linked by N—H⋯O and O—H⋯O hydrogen bonds to form an R (2) (2)(8) heterodimer motif. Pairs of adjacent motifs are further connected via N—H⋯O inter­actions to form a discrete centrosymmetric assembly. International Union of Crystallography 2008-06-19 /pmc/articles/PMC2961685/ /pubmed/21202925 http://dx.doi.org/10.1107/S1600536808018059 Text en © Johnston 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
Johnston, Andrea
Florence, Alastair J.
Fabbiani, Francesca J. A.
Shankland, Kenneth
Bedford, Colin T.
Cytenamide–butyric acid (1/1)
title Cytenamide–butyric acid (1/1)
title_full Cytenamide–butyric acid (1/1)
title_fullStr Cytenamide–butyric acid (1/1)
title_full_unstemmed Cytenamide–butyric acid (1/1)
title_short Cytenamide–butyric acid (1/1)
title_sort cytenamide–butyric acid (1/1)
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961685/
https://www.ncbi.nlm.nih.gov/pubmed/21202925
http://dx.doi.org/10.1107/S1600536808018059
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AT bedfordcolint cytenamidebutyricacid11

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