(E)-2-Meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate

The title compound, C(13)H(14)O(4), belongs to the class of α,β-unsaturated ketones, which have potential bactericidal, fungicidal, anti­tumor and anti-inflammatory properties. The C atoms and attached H atoms of the ethenyl part of the title mol­ecule are disordered over two orientations with refin...

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Detalles Bibliográficos
Autores principales: Zhang, Huoyun, Li, Shuqin, Shi, Xiaopeng
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962134/
https://www.ncbi.nlm.nih.gov/pubmed/21203216
http://dx.doi.org/10.1107/S1600536808021417
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author Zhang, Huoyun
Li, Shuqin
Shi, Xiaopeng
author_facet Zhang, Huoyun
Li, Shuqin
Shi, Xiaopeng
author_sort Zhang, Huoyun
collection PubMed
description The title compound, C(13)H(14)O(4), belongs to the class of α,β-unsaturated ketones, which have potential bactericidal, fungicidal, anti­tumor and anti-inflammatory properties. The C atoms and attached H atoms of the ethenyl part of the title mol­ecule are disordered over two orientations with refined occupancies of 0.583 (7) and 0.417 (3). Mol­ecules are connected by two inter­molecular C—H⋯O inter­actions, forming a dimer with [Image: see text] symmetry.
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spelling pubmed-29621342010-12-30 (E)-2-Meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate Zhang, Huoyun Li, Shuqin Shi, Xiaopeng Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(13)H(14)O(4), belongs to the class of α,β-unsaturated ketones, which have potential bactericidal, fungicidal, anti­tumor and anti-inflammatory properties. The C atoms and attached H atoms of the ethenyl part of the title mol­ecule are disordered over two orientations with refined occupancies of 0.583 (7) and 0.417 (3). Mol­ecules are connected by two inter­molecular C—H⋯O inter­actions, forming a dimer with [Image: see text] symmetry. International Union of Crystallography 2008-07-16 /pmc/articles/PMC2962134/ /pubmed/21203216 http://dx.doi.org/10.1107/S1600536808021417 Text en © Zhang 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
Zhang, Huoyun
Li, Shuqin
Shi, Xiaopeng
(E)-2-Meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate
title (E)-2-Meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate
title_full (E)-2-Meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate
title_fullStr (E)-2-Meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate
title_full_unstemmed (E)-2-Meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate
title_short (E)-2-Meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate
title_sort (e)-2-meth­oxy-4-(3-oxobut-1-en­yl)phenyl acetate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962134/
https://www.ncbi.nlm.nih.gov/pubmed/21203216
http://dx.doi.org/10.1107/S1600536808021417
work_keys_str_mv AT zhanghuoyun e2methoxy43oxobut1enylphenylacetate
AT lishuqin e2methoxy43oxobut1enylphenylacetate
AT shixiaopeng e2methoxy43oxobut1enylphenylacetate

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