| dc.contributor.author | Arslan, B | |
| dc.contributor.author | Kazak, C | |
| dc.contributor.author | Goker, H | |
| dc.date.accessioned | 2020-06-21T15:37:52Z | |
| dc.date.available | 2020-06-21T15:37:52Z | |
| dc.date.issued | 2004 | |
| dc.identifier.issn | 1600-5368 | |
| dc.identifier.uri | https://doi.org/10.1107/S1600536804027989 | |
| dc.identifier.uri | https://hdl.handle.net/20.500.12712/21308 | |
| dc.description | Kazak, Canan/0000-0003-2475-8775; goker, Hakan/0000-0002-9366-6949 | en_US |
| dc.description | WOS: 000225481600125 | en_US |
| dc.description.abstract | The 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 Angstrom. C-H...O interactions [C...O = 3.272 (5) Angstrom] link neighbouring molecules related by the 2(1) axis. | en_US |
| dc.language.iso | eng | en_US |
| dc.publisher | Blackwell Munksgaard | en_US |
| dc.relation.isversionof | 10.1107/S1600536804027989 | en_US |
| dc.rights | info:eu-repo/semantics/closedAccess | en_US |
| dc.title | 2,6-dimethyl-4H-1-benzopyran-4-one | en_US |
| dc.type | article | en_US |
| dc.contributor.department | OMÜ | en_US |
| dc.identifier.volume | 60 | en_US |
| dc.identifier.startpage | O2238 | en_US |
| dc.identifier.endpage | O2240 | en_US |
| dc.relation.journal | Acta Crystallographica Section E-Structure Reports Online | en_US |
| dc.relation.publicationcategory | Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı | en_US |
