anti-Ethyl aceto­hydroximate

In the crystal structure of the title compound, C(4)H(9)NO(2), the O—H⋯N hydrogen bonds link the mol­ecules into supra­molecular chains extending along the b-axis direction. The conformation of the NOH group in the nearly planar (r.m.s. deviation = 0.0546 Å) ethyl aceto­hydroximate mol­ecule is tran...

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Detalles Bibliográficos
Autores principales: Hachuła, Barbara, Polasz, Anna, Nowak, Maria, Kusz, Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884389/
https://www.ncbi.nlm.nih.gov/pubmed/24427053
http://dx.doi.org/10.1107/S1600536813022368
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author Hachuła, Barbara
Polasz, Anna
Nowak, Maria
Kusz, Joachim
author_facet Hachuła, Barbara
Polasz, Anna
Nowak, Maria
Kusz, Joachim
author_sort Hachuła, Barbara
collection PubMed
description In the crystal structure of the title compound, C(4)H(9)NO(2), the O—H⋯N hydrogen bonds link the mol­ecules into supra­molecular chains extending along the b-axis direction. The conformation of the NOH group in the nearly planar (r.m.s. deviation = 0.0546 Å) ethyl aceto­hydroximate mol­ecule is trans to N=C.
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spelling pubmed-38843892014-01-14 anti-Ethyl aceto­hydroximate Hachuła, Barbara Polasz, Anna Nowak, Maria Kusz, Joachim Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(4)H(9)NO(2), the O—H⋯N hydrogen bonds link the mol­ecules into supra­molecular chains extending along the b-axis direction. The conformation of the NOH group in the nearly planar (r.m.s. deviation = 0.0546 Å) ethyl aceto­hydroximate mol­ecule is trans to N=C. International Union of Crystallography 2013-08-21 /pmc/articles/PMC3884389/ /pubmed/24427053 http://dx.doi.org/10.1107/S1600536813022368 Text en © Hachuła et al. 2013 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
Hachuła, Barbara
Polasz, Anna
Nowak, Maria
Kusz, Joachim
anti-Ethyl aceto­hydroximate
title anti-Ethyl aceto­hydroximate
title_full anti-Ethyl aceto­hydroximate
title_fullStr anti-Ethyl aceto­hydroximate
title_full_unstemmed anti-Ethyl aceto­hydroximate
title_short anti-Ethyl aceto­hydroximate
title_sort anti-ethyl aceto­hydroximate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3884389/
https://www.ncbi.nlm.nih.gov/pubmed/24427053
http://dx.doi.org/10.1107/S1600536813022368
work_keys_str_mv AT hachułabarbara antiethylacetohydroximate
AT polaszanna antiethylacetohydroximate
AT nowakmaria antiethylacetohydroximate
AT kuszjoachim antiethylacetohydroximate

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