(3Z)-4-Methyl-9-(4-methyl­benzene­sulfon­yl)-N-phenyl-3H,9H-thio­pyrano[3,4-b]indol-3-imine

dc.contributor.authorDassonneville, Benjamin
dc.contributor.authorDetert, Heiner
dc.contributor.authorSchollmeyer, Dieter
dc.date.accessioned2025-12-12T11:46:13Z
dc.date.issued2025
dc.description.abstractThe title indolothiopyrane imine, C25H20N2O2S2, which was prepared by a [2 + 2 + 2] cycloaddition reaction, crystallizes with two molecules in the asymmetric unit. Both adopt the shape of a staircase with two steps, consolidated by intramolecular C—H⋯O interactions.en
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/13944
dc.language.isoeng
dc.rightsCC-BY-4.0
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subject.ddc540 Chemiede
dc.subject.ddc540 Chemistry and allied sciencesen
dc.title(3Z)-4-Methyl-9-(4-methyl­benzene­sulfon­yl)-N-phenyl-3H,9H-thio­pyrano[3,4-b]indol-3-imineen
dc.typeZeitschriftenaufsatz
jgu.identifier.uuid809799f2-419b-4e04-9a37-fb2526fbb96d
jgu.journal.issue5
jgu.journal.titleIUCrData
jgu.journal.volume10
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.pages.alternativex250475
jgu.publisher.doi10.1107/S2414314625004754
jgu.publisher.issn2414-3146
jgu.publisher.nameIUCr
jgu.publisher.placeChester
jgu.publisher.year2025
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode540
jgu.subject.dfgNaturwissenschaften
jgu.type.dinitypeArticleen_GB
jgu.type.resourceText
jgu.type.versionPublished version

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