(E)-3-Chloro-N′-hy­droxy­benzene-1-carboximidamide

The title compound, C(7)H(7)ClN(2)O, crystallizes with two independent mol­ecules in the asymmetric unit. The compound adopts an E configuration across the C=N double bond, as the –OH group and the benzene ring are on opposite sides of the double bond while the H atom of the hy­droxy group is direct...

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Detalles Bibliográficos
Autores principales: Sreenivasa, S., ManojKumar, K. E., Suchetan, P. A., Mohan, N. R, Palakshamurthy, B. S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588992/
https://www.ncbi.nlm.nih.gov/pubmed/23476228
http://dx.doi.org/10.1107/S1600536812046612
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author Sreenivasa, S.
ManojKumar, K. E.
Suchetan, P. A.
Mohan, N. R
Palakshamurthy, B. S.
author_facet Sreenivasa, S.
ManojKumar, K. E.
Suchetan, P. A.
Mohan, N. R
Palakshamurthy, B. S.
author_sort Sreenivasa, S.
collection PubMed
description The title compound, C(7)H(7)ClN(2)O, crystallizes with two independent mol­ecules in the asymmetric unit. The compound adopts an E configuration across the C=N double bond, as the –OH group and the benzene ring are on opposite sides of the double bond while the H atom of the hy­droxy group is directed away from the –NH(2) group. In the crystal, mol­ecules are linked to one another through O—H⋯N and N—H⋯O hydrogen bonds, forming chains along [010].
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spelling pubmed-35889922013-03-08 (E)-3-Chloro-N′-hy­droxy­benzene-1-carboximidamide Sreenivasa, S. ManojKumar, K. E. Suchetan, P. A. Mohan, N. R Palakshamurthy, B. S. Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(7)H(7)ClN(2)O, crystallizes with two independent mol­ecules in the asymmetric unit. The compound adopts an E configuration across the C=N double bond, as the –OH group and the benzene ring are on opposite sides of the double bond while the H atom of the hy­droxy group is directed away from the –NH(2) group. In the crystal, mol­ecules are linked to one another through O—H⋯N and N—H⋯O hydrogen bonds, forming chains along [010]. International Union of Crystallography 2012-11-24 /pmc/articles/PMC3588992/ /pubmed/23476228 http://dx.doi.org/10.1107/S1600536812046612 Text en © Sreenivasa et al. 2012 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
Sreenivasa, S.
ManojKumar, K. E.
Suchetan, P. A.
Mohan, N. R
Palakshamurthy, B. S.
(E)-3-Chloro-N′-hy­droxy­benzene-1-carboximidamide
title (E)-3-Chloro-N′-hy­droxy­benzene-1-carboximidamide
title_full (E)-3-Chloro-N′-hy­droxy­benzene-1-carboximidamide
title_fullStr (E)-3-Chloro-N′-hy­droxy­benzene-1-carboximidamide
title_full_unstemmed (E)-3-Chloro-N′-hy­droxy­benzene-1-carboximidamide
title_short (E)-3-Chloro-N′-hy­droxy­benzene-1-carboximidamide
title_sort (e)-3-chloro-n′-hy­droxy­benzene-1-carboximidamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3588992/
https://www.ncbi.nlm.nih.gov/pubmed/23476228
http://dx.doi.org/10.1107/S1600536812046612
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AT palakshamurthybs e3chloronhydroxybenzene1carboximidamide

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