(E)-1-(2-Amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one

The mol­ecule of the title heteroaryl chalcone derivative, C(13)H(11)NOS, exists in a trans-configuaration and is almost planar with a dihedral angle of 3.73 (8)° between the phenyl and thio­phene rings. An intra­molecular N—H⋯O hydrogen bond generates an S(6) ring motif. In the crystal, two adjacen...

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Detalles Bibliográficos
Autores principales: Chantrapromma, Suchada, Ruanwas, Pumsak, Boonnak, Nawong, Fun, Hoong-Kun
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/PMC3772449/
https://www.ncbi.nlm.nih.gov/pubmed/24046592
http://dx.doi.org/10.1107/S1600536813014189
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author Chantrapromma, Suchada
Ruanwas, Pumsak
Boonnak, Nawong
Fun, Hoong-Kun
author_facet Chantrapromma, Suchada
Ruanwas, Pumsak
Boonnak, Nawong
Fun, Hoong-Kun
author_sort Chantrapromma, Suchada
collection PubMed
description The mol­ecule of the title heteroaryl chalcone derivative, C(13)H(11)NOS, exists in a trans-configuaration and is almost planar with a dihedral angle of 3.73 (8)° between the phenyl and thio­phene rings. An intra­molecular N—H⋯O hydrogen bond generates an S(6) ring motif. In the crystal, two adjacent mol­ecules are linked into a dimer in an anti-parallel face-to-face manner by a pair of C—H⋯O inter­actions. Neighboring dimers are further linked into chains along the c-axis direction by N—H⋯N hydrogen bonds.
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spelling pubmed-37724492013-09-17 (E)-1-(2-Amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one Chantrapromma, Suchada Ruanwas, Pumsak Boonnak, Nawong Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title heteroaryl chalcone derivative, C(13)H(11)NOS, exists in a trans-configuaration and is almost planar with a dihedral angle of 3.73 (8)° between the phenyl and thio­phene rings. An intra­molecular N—H⋯O hydrogen bond generates an S(6) ring motif. In the crystal, two adjacent mol­ecules are linked into a dimer in an anti-parallel face-to-face manner by a pair of C—H⋯O inter­actions. Neighboring dimers are further linked into chains along the c-axis direction by N—H⋯N hydrogen bonds. International Union of Crystallography 2013-06-08 /pmc/articles/PMC3772449/ /pubmed/24046592 http://dx.doi.org/10.1107/S1600536813014189 Text en © Chantrapromma 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
Chantrapromma, Suchada
Ruanwas, Pumsak
Boonnak, Nawong
Fun, Hoong-Kun
(E)-1-(2-Amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one
title (E)-1-(2-Amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one
title_full (E)-1-(2-Amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one
title_fullStr (E)-1-(2-Amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one
title_full_unstemmed (E)-1-(2-Amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one
title_short (E)-1-(2-Amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one
title_sort (e)-1-(2-amino­phen­yl)-3-(thio­phen-2-yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3772449/
https://www.ncbi.nlm.nih.gov/pubmed/24046592
http://dx.doi.org/10.1107/S1600536813014189
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AT funhoongkun e12aminophenyl3thiophen2ylprop2en1one

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