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dc.contributor.authorMałecka, Magdalena
dc.contributor.authorCiołkowski, Michał
dc.contributor.authorBudzisz, Elżbieta
dc.date.accessioned2022-02-01T13:51:57Z
dc.date.available2022-02-01T13:51:57Z
dc.date.issued2010
dc.identifier.issn1600-5368
dc.identifier.urihttp://hdl.handle.net/11089/40543
dc.descriptionThe title mol­ecule, C20H21NO6, adopts a keto–amine tautomeric form. An intra­molecular N—H⋯O hydrogen bond, classified as a resonanse-assisted hydrogen bond, influences the mol­ecular conformation; the two benzene rings form a dihedral angle of 24.6 (1)°. In the crystal structure, weak inter­molecular C—H⋯O hydrogen bonds link mol­ecules into chains propagating along [001].pl_PL
dc.description.sponsorshipFinancial support from the University of Łódź and the Medical University of Łódź (grant No. 505/710 to MM and No. 502–13-701 to MC) is gratefully acknowledged. The authors thank Dr Oliver Presly from Oxford Diffraction for collecting the data.pl_PL
dc.language.isoenpl_PL
dc.publisherInternational Union of Crystallographypl_PL
dc.relation.ispartofseriesActa Crystallographica Section E: Crystallographic Communications;66
dc.rightsUznanie autorstwa 4.0 Międzynarodowe*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectsingle-crystal X-ray studypl_PL
dc.subjectT = 100 Kpl_PL
dc.subjectmean (C–C) = 0.002 Apl_PL
dc.subjectR factor = 0.037pl_PL
dc.subjectwR factor = 0.101pl_PL
dc.subjectdata-to-parameter ratio = 11.5pl_PL
dc.title2-Methoxy-3-[(3,4,5-trimethoxyanilino)- methylidene]-3,4-dihydro-2H-1-benzopyran-4-onepl_PL
dc.typeArticlepl_PL
dc.page.numbero246pl_PL
dc.contributor.authorAffiliationDepartment of Crystallography and Crystal Chemistry, University of Łódź, Pomorska 149/153, PL-90236 Łódź, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Cosmetic Raw Materials Chemistry, Faculty of Pharmacy, Medical University of Łódź, Muszyńskiego 1, PL-90151 Łódź, Polandpl_PL
dc.contributor.authorAffiliationDepartment of Cosmetic Raw Materials Chemistry, Faculty of Pharmacy, Medical University of Łódź, Muszyńskiego 1, PL-90151 Łódź, Polandpl_PL
dc.referencesBertolasi, V., Gilli, P., Ferretti, V. & Gilli, G. (1998). Acta Cryst. B54, 50–65.pl_PL
dc.referencesGilli, P., Bertolasi, V., Ferretti, V. & Gilli, G. (1994). J. Am. Chem. Soc. 116, 909–915.pl_PL
dc.referencesKhan, K. M., Ambreen, N., Hussain, S., Perveen, S. & Choudhary, M. I. (2009). Bioorg. Med. Chem. 17, 2983–2988.pl_PL
dc.referencesMałecka, M. (2007). J. Mol. Struct. 831, 135–143.pl_PL
dc.referencesMałecka, M. & Budzisz, E. (2006). Acta Cryst. E62, o5058–o5060.pl_PL
dc.referencesOxford Diffraction (2009). CrysAlis CCD and CrysAlis RED. Oxford Diffraction Ltd, Yarnton, England.pl_PL
dc.referencesSheldrick, G. M. (2008). Acta Cryst. A64, 112–122.pl_PL
dc.referencesSpek, A. L. (2009). Acta Cryst. D65, 148–155.pl_PL
dc.contributor.authorEmailmalecka@uni.lodz.plpl_PL
dc.identifier.doi10.1107/S1600536809054889
dc.relation.volume1pl_PL
dc.disciplinenauki chemicznepl_PL


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Uznanie autorstwa 4.0 Międzynarodowe
Except where otherwise noted, this item's license is described as Uznanie autorstwa 4.0 Międzynarodowe