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...

Descripción completa

Detalles Bibliográficos
Autores principales: Augustine, T., Vithiya, Scholastica Mary, Ramkumar, V., Kanakam, Charles C.
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