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2,6-Dimethyl-4H-1-benzopyran-4-one

dc.contributor.authorGöker, Hakan
dc.date.accessioned2020-02-15T14:08:50Z
dc.date.available2020-02-15T14:08:50Z
dc.date.issued2004
dc.identifier.urihttps://doi.org/10.1107/S1600536804027989tr_TR
dc.identifier.urihttp://hdl.handle.net/20.500.12575/69578
dc.description.abstractThe title compound, C11H10O2, belongs to the class of 4-benzopyrones (also known as chromen-4-ones) with potentially diverse pharmacological activities. It was synthesized by acyl­ation of 2-hydroxy-4-methyl­aceto­phenone with ethyl acetate in the presence of sodium hydride and subsequent cyclization by hydro­chloric acid. All non-H atoms of the substituted bicyclic mol­ecule are coplanar within 0.03 Å. C-H...O interactions [C...O = 3.272 (5) Å] link neighbouring mol­ecules related by the 21 axis
dc.language.isoentr_TR
dc.relation.isversionof10.1107/S1600536804027989tr_TR
dc.rightsCC0 1.0 Universal*
dc.rights.urihttp://creativecommons.org/publicdomain/zero/1.0/*
dc.subjectSingle-crystal X-ray studytr_TR
dc.subjectwR factor = 0.184tr_TR
dc.subjectR factor = 0.054tr_TR
dc.subjectData-to-parameter ratio = 12.9tr_TR
dc.title2,6-Dimethyl-4H-1-benzopyran-4-onetr_TR
dc.typeArticletr_TR
dc.relation.journalActa Crystallographica Section E: Structure Reports Onlinetr_TR
dc.contributor.departmentEczacılık Fakültesitr_TR
dc.identifier.volume60tr_TR
dc.identifier.issue12tr_TR
dc.identifier.startpageo2238tr_TR
dc.identifier.endpageo2240tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıtr_TR
dc.identifier.issn/e-issn1600-5368
dc.description.indexScopus
dc.description.indexWos


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