(E)-1-(2-Fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one

In the title heteroaryl chalcone derivative, C(16)H(16)O(5), the dihedral angle between the furan and benzene rings is 14.45 (6)°. The three meth­oxy groups are almost coplanar with their attached benzene ring [C—C—O—C torsion angles = 2.07 (17), −5.04 (17) and 2.85 (16)°]. An intra­molecular C—H⋯O...

Descripción completa

Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Suwunwong, Thitipone, Chantrapromma, Suchada, Karalai, Chatchanok
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983191/
https://www.ncbi.nlm.nih.gov/pubmed/21587546
http://dx.doi.org/10.1107/S1600536810035762
_version_ 1782191822330658816
author Fun, Hoong-Kun
Suwunwong, Thitipone
Chantrapromma, Suchada
Karalai, Chatchanok
author_facet Fun, Hoong-Kun
Suwunwong, Thitipone
Chantrapromma, Suchada
Karalai, Chatchanok
author_sort Fun, Hoong-Kun
collection PubMed
description In the title heteroaryl chalcone derivative, C(16)H(16)O(5), the dihedral angle between the furan and benzene rings is 14.45 (6)°. The three meth­oxy groups are almost coplanar with their attached benzene ring [C—C—O—C torsion angles = 2.07 (17), −5.04 (17) and 2.85 (16)°]. An intra­molecular C—H⋯O hydrogen bond occurs. In the crystal, adjacent mol­ecules are linked into X-shaped chains along the c axis by weak C—H⋯O(enone) inter­actions. These chains are stacked along the b axis. C⋯O [3.3308 (13)–3.4123 (14) Å] short contacts are also observed.
format Text
id pubmed-2983191
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29831912010-12-30 (E)-1-(2-Fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one Fun, Hoong-Kun Suwunwong, Thitipone Chantrapromma, Suchada Karalai, Chatchanok Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title heteroaryl chalcone derivative, C(16)H(16)O(5), the dihedral angle between the furan and benzene rings is 14.45 (6)°. The three meth­oxy groups are almost coplanar with their attached benzene ring [C—C—O—C torsion angles = 2.07 (17), −5.04 (17) and 2.85 (16)°]. An intra­molecular C—H⋯O hydrogen bond occurs. In the crystal, adjacent mol­ecules are linked into X-shaped chains along the c axis by weak C—H⋯O(enone) inter­actions. These chains are stacked along the b axis. C⋯O [3.3308 (13)–3.4123 (14) Å] short contacts are also observed. International Union of Crystallography 2010-09-15 /pmc/articles/PMC2983191/ /pubmed/21587546 http://dx.doi.org/10.1107/S1600536810035762 Text en © Fun et al. 2010 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
Fun, Hoong-Kun
Suwunwong, Thitipone
Chantrapromma, Suchada
Karalai, Chatchanok
(E)-1-(2-Fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one
title (E)-1-(2-Fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one
title_full (E)-1-(2-Fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one
title_fullStr (E)-1-(2-Fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one
title_full_unstemmed (E)-1-(2-Fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one
title_short (E)-1-(2-Fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one
title_sort (e)-1-(2-fur­yl)-3-(2,4,6-trimeth­oxy­phen­yl)prop-2-en-1-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983191/
https://www.ncbi.nlm.nih.gov/pubmed/21587546
http://dx.doi.org/10.1107/S1600536810035762
work_keys_str_mv AT funhoongkun e12furyl3246trimethoxyphenylprop2en1one
AT suwunwongthitipone e12furyl3246trimethoxyphenylprop2en1one
AT chantraprommasuchada e12furyl3246trimethoxyphenylprop2en1one
AT karalaichatchanok e12furyl3246trimethoxyphenylprop2en1one

Ejemplares similares