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4-(Oct­yloxy)phenyl 2-oxo-2H-chromene-3-carboxyl­ate

In the title compound, C(24)H(26)O(5), the 2H-chromene ring system is essentially planar, with a maximum deviation of 0.029 (2) Å from the best-fit mean plane incorporating both rings. The dihedral angle between the 2H-chromene ring system and the benzene ring is 21.00 (1)°. In the crystal, pairs of...

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Autores principales: Palakshamurthy, B. S., Sreenivasa, S., Srinivasa, H. T., Roopashree, K. R., Devarajegowda, H. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569748/
https://www.ncbi.nlm.nih.gov/pubmed/23424494
http://dx.doi.org/10.1107/S1600536813000214
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author Palakshamurthy, B. S.
Sreenivasa, S.
Srinivasa, H. T.
Roopashree, K. R.
Devarajegowda, H. C.
author_facet Palakshamurthy, B. S.
Sreenivasa, S.
Srinivasa, H. T.
Roopashree, K. R.
Devarajegowda, H. C.
author_sort Palakshamurthy, B. S.
collection PubMed
description In the title compound, C(24)H(26)O(5), the 2H-chromene ring system is essentially planar, with a maximum deviation of 0.029 (2) Å from the best-fit mean plane incorporating both rings. The dihedral angle between the 2H-chromene ring system and the benzene ring is 21.00 (1)°. In the crystal, pairs of C—H⋯O hydrogen bonds generate an R (2) (2)(8) ring pattern. These contacts are bolstered by weaker bifurcated C—H⋯O hydrogen bonds.
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spelling pubmed-35697482013-02-19 4-(Oct­yloxy)phenyl 2-oxo-2H-chromene-3-carboxyl­ate Palakshamurthy, B. S. Sreenivasa, S. Srinivasa, H. T. Roopashree, K. R. Devarajegowda, H. C. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(24)H(26)O(5), the 2H-chromene ring system is essentially planar, with a maximum deviation of 0.029 (2) Å from the best-fit mean plane incorporating both rings. The dihedral angle between the 2H-chromene ring system and the benzene ring is 21.00 (1)°. In the crystal, pairs of C—H⋯O hydrogen bonds generate an R (2) (2)(8) ring pattern. These contacts are bolstered by weaker bifurcated C—H⋯O hydrogen bonds. International Union of Crystallography 2013-01-09 /pmc/articles/PMC3569748/ /pubmed/23424494 http://dx.doi.org/10.1107/S1600536813000214 Text en © Palakshamurthy 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
Palakshamurthy, B. S.
Sreenivasa, S.
Srinivasa, H. T.
Roopashree, K. R.
Devarajegowda, H. C.
4-(Oct­yloxy)phenyl 2-oxo-2H-chromene-3-carboxyl­ate
title 4-(Oct­yloxy)phenyl 2-oxo-2H-chromene-3-carboxyl­ate
title_full 4-(Oct­yloxy)phenyl 2-oxo-2H-chromene-3-carboxyl­ate
title_fullStr 4-(Oct­yloxy)phenyl 2-oxo-2H-chromene-3-carboxyl­ate
title_full_unstemmed 4-(Oct­yloxy)phenyl 2-oxo-2H-chromene-3-carboxyl­ate
title_short 4-(Oct­yloxy)phenyl 2-oxo-2H-chromene-3-carboxyl­ate
title_sort 4-(oct­yloxy)phenyl 2-oxo-2h-chromene-3-carboxyl­ate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569748/
https://www.ncbi.nlm.nih.gov/pubmed/23424494
http://dx.doi.org/10.1107/S1600536813000214
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