Cargando…
3-Benzylidene-6-methoxychroman-4-one
In the title compound, C(17)H(14)O(3), the dihedral angle between the phenyl ring and the benzene ring of the chromanone moiety is 67.78 (3)°. The six-membered heterocyclic ring of the chromanone moiety adopts a half-chair conformation. The structure is stabilized by weak intermolecular C—H⋯O inter...
Autores principales: | , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959532/ https://www.ncbi.nlm.nih.gov/pubmed/21580945 http://dx.doi.org/10.1107/S1600536808031541 |
_version_ | 1782188522101276672 |
---|---|
author | Augustine, T. Vithiya, Scholastica Mary Ramkumar, V. Kanakam, Charles C. |
author_facet | Augustine, T. Vithiya, Scholastica Mary Ramkumar, V. Kanakam, Charles C. |
author_sort | Augustine, T. |
collection | PubMed |
description | In the title compound, C(17)H(14)O(3), the dihedral angle between the phenyl ring and the benzene ring of the chromanone moiety is 67.78 (3)°. The six-membered heterocyclic ring of the chromanone moiety adopts a half-chair conformation. The structure is stabilized by weak intermolecular C—H⋯O interactions that link the molecules into inversion dimers. |
format | Text |
id | pubmed-2959532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29595322010-12-30 3-Benzylidene-6-methoxychroman-4-one Augustine, T. Vithiya, Scholastica Mary Ramkumar, V. Kanakam, Charles C. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(17)H(14)O(3), the dihedral angle between the phenyl ring and the benzene ring of the chromanone moiety is 67.78 (3)°. The six-membered heterocyclic ring of the chromanone moiety adopts a half-chair conformation. The structure is stabilized by weak intermolecular C—H⋯O interactions that link the molecules into inversion dimers. International Union of Crystallography 2008-10-09 /pmc/articles/PMC2959532/ /pubmed/21580945 http://dx.doi.org/10.1107/S1600536808031541 Text en © Augustine 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 Augustine, T. Vithiya, Scholastica Mary Ramkumar, V. Kanakam, Charles C. 3-Benzylidene-6-methoxychroman-4-one |
title | 3-Benzylidene-6-methoxychroman-4-one |
title_full | 3-Benzylidene-6-methoxychroman-4-one |
title_fullStr | 3-Benzylidene-6-methoxychroman-4-one |
title_full_unstemmed | 3-Benzylidene-6-methoxychroman-4-one |
title_short | 3-Benzylidene-6-methoxychroman-4-one |
title_sort | 3-benzylidene-6-methoxychroman-4-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2959532/ https://www.ncbi.nlm.nih.gov/pubmed/21580945 http://dx.doi.org/10.1107/S1600536808031541 |
work_keys_str_mv | AT augustinet 3benzylidene6methoxychroman4one AT vithiyascholasticamary 3benzylidene6methoxychroman4one AT ramkumarv 3benzylidene6methoxychroman4one AT kanakamcharlesc 3benzylidene6methoxychroman4one |