Cargando…

2-(4-Chloro­phen­yl)-6-meth­oxy­chroman-4-one

In the title mol­ecule, C(16)H(13)Cl O(3), the two aromatic rings form a dihedral angle of 65.3 (1)°. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers, which are further packed into columns propagating in [100] by weak C—H⋯π inter­ac...

Descripción completa

Detalles Bibliográficos
Autores principales: Jasinski, Jerry P., Pek, Albert E., Narayana, B., Yathirajan, H. S., Nayak, Prakash S.
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983332/
https://www.ncbi.nlm.nih.gov/pubmed/21587536
http://dx.doi.org/10.1107/S1600536810035816
_version_ 1782191856423010304
author Jasinski, Jerry P.
Pek, Albert E.
Narayana, B.
Yathirajan, H. S.
Nayak, Prakash S.
author_facet Jasinski, Jerry P.
Pek, Albert E.
Narayana, B.
Yathirajan, H. S.
Nayak, Prakash S.
author_sort Jasinski, Jerry P.
collection PubMed
description In the title mol­ecule, C(16)H(13)Cl O(3), the two aromatic rings form a dihedral angle of 65.3 (1)°. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers, which are further packed into columns propagating in [100] by weak C—H⋯π inter­actions.
format Text
id pubmed-2983332
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-29833322010-12-30 2-(4-Chloro­phen­yl)-6-meth­oxy­chroman-4-one Jasinski, Jerry P. Pek, Albert E. Narayana, B. Yathirajan, H. S. Nayak, Prakash S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title mol­ecule, C(16)H(13)Cl O(3), the two aromatic rings form a dihedral angle of 65.3 (1)°. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers, which are further packed into columns propagating in [100] by weak C—H⋯π inter­actions. International Union of Crystallography 2010-09-11 /pmc/articles/PMC2983332/ /pubmed/21587536 http://dx.doi.org/10.1107/S1600536810035816 Text en © Jasinski 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
Jasinski, Jerry P.
Pek, Albert E.
Narayana, B.
Yathirajan, H. S.
Nayak, Prakash S.
2-(4-Chloro­phen­yl)-6-meth­oxy­chroman-4-one
title 2-(4-Chloro­phen­yl)-6-meth­oxy­chroman-4-one
title_full 2-(4-Chloro­phen­yl)-6-meth­oxy­chroman-4-one
title_fullStr 2-(4-Chloro­phen­yl)-6-meth­oxy­chroman-4-one
title_full_unstemmed 2-(4-Chloro­phen­yl)-6-meth­oxy­chroman-4-one
title_short 2-(4-Chloro­phen­yl)-6-meth­oxy­chroman-4-one
title_sort 2-(4-chloro­phen­yl)-6-meth­oxy­chroman-4-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2983332/
https://www.ncbi.nlm.nih.gov/pubmed/21587536
http://dx.doi.org/10.1107/S1600536810035816
work_keys_str_mv AT jasinskijerryp 24chlorophenyl6methoxychroman4one
AT pekalberte 24chlorophenyl6methoxychroman4one
AT narayanab 24chlorophenyl6methoxychroman4one
AT yathirajanhs 24chlorophenyl6methoxychroman4one
AT nayakprakashs 24chlorophenyl6methoxychroman4one