6-Hy­droxy-5,7,8-trimethyl­chroman-2-one

The title compound, C(12)H(14)O(3), consists of a chromanone unit with an –OH substituent at the 4-position and methyl substituents on the remaining C atoms of the aromatic ring. The fused pyran­one ring adopts a distorted envelope conformation with the methyl­ene group adjacent to the carbonyl carb...

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Autores principales: Goswami, Shailesh K., Hanton, Lyall R., McAdam, C. John, Moratti, Stephen C., Simpson, Jim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151777/
https://www.ncbi.nlm.nih.gov/pubmed/21836979
http://dx.doi.org/10.1107/S1600536811019982
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author Goswami, Shailesh K.
Hanton, Lyall R.
McAdam, C. John
Moratti, Stephen C.
Simpson, Jim
author_facet Goswami, Shailesh K.
Hanton, Lyall R.
McAdam, C. John
Moratti, Stephen C.
Simpson, Jim
author_sort Goswami, Shailesh K.
collection PubMed
description The title compound, C(12)H(14)O(3), consists of a chromanone unit with an –OH substituent at the 4-position and methyl substituents on the remaining C atoms of the aromatic ring. The fused pyran­one ring adopts a distorted envelope conformation with the methyl­ene group adjacent to the carbonyl carbon as the flap atom. The crystal structure is stabilized by classical O—H⋯O hydrogen bonds and weak C—H⋯O and C—H⋯π inter­actions, generating a three-dimensional network.
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spelling pubmed-31517772011-08-11 6-Hy­droxy-5,7,8-trimethyl­chroman-2-one Goswami, Shailesh K. Hanton, Lyall R. McAdam, C. John Moratti, Stephen C. Simpson, Jim Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(12)H(14)O(3), consists of a chromanone unit with an –OH substituent at the 4-position and methyl substituents on the remaining C atoms of the aromatic ring. The fused pyran­one ring adopts a distorted envelope conformation with the methyl­ene group adjacent to the carbonyl carbon as the flap atom. The crystal structure is stabilized by classical O—H⋯O hydrogen bonds and weak C—H⋯O and C—H⋯π inter­actions, generating a three-dimensional network. International Union of Crystallography 2011-06-04 /pmc/articles/PMC3151777/ /pubmed/21836979 http://dx.doi.org/10.1107/S1600536811019982 Text en © Goswami et al. 2011 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
Goswami, Shailesh K.
Hanton, Lyall R.
McAdam, C. John
Moratti, Stephen C.
Simpson, Jim
6-Hy­droxy-5,7,8-trimethyl­chroman-2-one
title 6-Hy­droxy-5,7,8-trimethyl­chroman-2-one
title_full 6-Hy­droxy-5,7,8-trimethyl­chroman-2-one
title_fullStr 6-Hy­droxy-5,7,8-trimethyl­chroman-2-one
title_full_unstemmed 6-Hy­droxy-5,7,8-trimethyl­chroman-2-one
title_short 6-Hy­droxy-5,7,8-trimethyl­chroman-2-one
title_sort 6-hy­droxy-5,7,8-trimethyl­chroman-2-one
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3151777/
https://www.ncbi.nlm.nih.gov/pubmed/21836979
http://dx.doi.org/10.1107/S1600536811019982
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