(Z)-3-(1-Hy­droxy-3-oxobut-1-en­yl)-6-nitro-2H-chromen-2-one

In the title compound, C(13)H(9)NO(6), the coumarin system has the benzene ring aligned at 0.61 (18)° with respect to the pyrone ring. An intra­molecular O—H⋯O hydrogen bond stabilizes the mol­ecular conformation and a C—H⋯O contact also occurs. In the crystal, weak C—H⋯O inter­actions link the mol­...

Descripción completa

Detalles Bibliográficos
Autores principales: Topno, Nishith Saurav, Tangeti, Venkataswamy, Rao, H. Surya Prakash, Krishna, R.
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/PMC3569810/
https://www.ncbi.nlm.nih.gov/pubmed/23424556
http://dx.doi.org/10.1107/S1600536812051872
_version_ 1782258968053153792
author Topno, Nishith Saurav
Tangeti, Venkataswamy
Rao, H. Surya Prakash
Krishna, R.
author_facet Topno, Nishith Saurav
Tangeti, Venkataswamy
Rao, H. Surya Prakash
Krishna, R.
author_sort Topno, Nishith Saurav
collection PubMed
description In the title compound, C(13)H(9)NO(6), the coumarin system has the benzene ring aligned at 0.61 (18)° with respect to the pyrone ring. An intra­molecular O—H⋯O hydrogen bond stabilizes the mol­ecular conformation and a C—H⋯O contact also occurs. In the crystal, weak C—H⋯O inter­actions link the mol­ecules, forming inversion dimers.
format Online
Article
Text
id pubmed-3569810
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-35698102013-02-19 (Z)-3-(1-Hy­droxy-3-oxobut-1-en­yl)-6-nitro-2H-chromen-2-one Topno, Nishith Saurav Tangeti, Venkataswamy Rao, H. Surya Prakash Krishna, R. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(9)NO(6), the coumarin system has the benzene ring aligned at 0.61 (18)° with respect to the pyrone ring. An intra­molecular O—H⋯O hydrogen bond stabilizes the mol­ecular conformation and a C—H⋯O contact also occurs. In the crystal, weak C—H⋯O inter­actions link the mol­ecules, forming inversion dimers. International Union of Crystallography 2013-01-23 /pmc/articles/PMC3569810/ /pubmed/23424556 http://dx.doi.org/10.1107/S1600536812051872 Text en © Topno 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
Topno, Nishith Saurav
Tangeti, Venkataswamy
Rao, H. Surya Prakash
Krishna, R.
(Z)-3-(1-Hy­droxy-3-oxobut-1-en­yl)-6-nitro-2H-chromen-2-one
title (Z)-3-(1-Hy­droxy-3-oxobut-1-en­yl)-6-nitro-2H-chromen-2-one
title_full (Z)-3-(1-Hy­droxy-3-oxobut-1-en­yl)-6-nitro-2H-chromen-2-one
title_fullStr (Z)-3-(1-Hy­droxy-3-oxobut-1-en­yl)-6-nitro-2H-chromen-2-one
title_full_unstemmed (Z)-3-(1-Hy­droxy-3-oxobut-1-en­yl)-6-nitro-2H-chromen-2-one
title_short (Z)-3-(1-Hy­droxy-3-oxobut-1-en­yl)-6-nitro-2H-chromen-2-one
title_sort (z)-3-(1-hy­droxy-3-oxobut-1-en­yl)-6-nitro-2h-chromen-2-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569810/
https://www.ncbi.nlm.nih.gov/pubmed/23424556
http://dx.doi.org/10.1107/S1600536812051872
work_keys_str_mv AT topnonishithsaurav z31hydroxy3oxobut1enyl6nitro2hchromen2one
AT tangetivenkataswamy z31hydroxy3oxobut1enyl6nitro2hchromen2one
AT raohsuryaprakash z31hydroxy3oxobut1enyl6nitro2hchromen2one
AT krishnar z31hydroxy3oxobut1enyl6nitro2hchromen2one

Ejemplares similares