Gutenberg Open Science: 3-(4-Hexyloxyphenyl)-1,2,4-triazolo[3,4-b]benzothiazole

Please use this identifier to cite or link to this item: http://doi.org/10.25358/openscience-7946

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DC Field	Value	Language
dc.contributor.author	Schollmeyer, Dieter	-
dc.contributor.author	Detert, Heiner	-
dc.date.accessioned	2022-10-12T09:58:57Z	-
dc.date.available	2022-10-12T09:58:57Z	-
dc.date.issued	2014	-
dc.identifier.uri	https://openscience.ub.uni-mainz.de/handle/20.500.12030/7961	-
dc.description.abstract	The title compound, C20H21N3OS, was prepared by Huisgen reaction of 5-(4-hexyl-oxyphen-yl)tetra-zole and chloro-benzo-thia-zole. The essentially planar benzo-thia-zolotriazole framework [maximum deviation from the mean plane of 0.077 (1) A for the bridgehead N atom] and the phenyl ring form a dihedral angle of 53.34 (5) degrees . The hex-yloxy chain adopts a gauche-all-anti conformation. The intra-centroid separation of 3.7258 (8) A between the triazole and benzene rings is the closest contact between individual mol-ecules in the crystal.	en_GB
dc.description.sponsorship	DFG, Open Access-Publizieren Universität Mainz / Universitätsmedizin	de
dc.language.iso	eng	de
dc.rights	CC BY	*
dc.rights.uri	https://creativecommons.org/licenses/by/2.0/uk/	*
dc.subject.ddc	540 Chemie	de_DE
dc.subject.ddc	540 Chemistry and allied sciences	en_GB
dc.title	3-(4-Hexyloxyphenyl)-1,2,4-triazolo[3,4-b]benzothiazole	en_GB
dc.type	Zeitschriftenaufsatz	de
dc.identifier.doi	http://doi.org/10.25358/openscience-7946	-
jgu.type.dinitype	article	en_GB
jgu.type.version	Published version	de
jgu.type.resource	Text	de
jgu.organisation.department	FB 09 Chemie, Pharmazie u. Geowissensch.	de
jgu.organisation.number	7950	-
jgu.organisation.name	Johannes Gutenberg-Universität Mainz	-
jgu.rights.accessrights	openAccess	-
jgu.journal.title	Acta crystallographica : Section E, Structure reports online	de
jgu.journal.volume	70	de
jgu.journal.issue	3	de
jgu.pages.alternative	o247	de
jgu.publisher.year	2014	-
jgu.publisher.name	Munksgaard	de
jgu.publisher.place	Copenhagen	de
jgu.publisher.uri	http://dx.doi.org/10.1107/S1600536814002153	de
jgu.publisher.issn	1600-5368	de
jgu.organisation.place	Mainz	-
jgu.identifier.pmid	24764967	-
jgu.subject.ddccode	540	de
opus.date.modified	2018-08-08T07:28:57Z	-
opus.subject.dfgcode	00-000	-
opus.organisation.string	FB 09: Chemie, Pharmazie und Geowissenschaften: Institut für Organische Chemie	de_DE
opus.identifier.opusid	25951	-
opus.importsource	pubmed	-
opus.institute.number	0905	-
opus.metadataonly	false	-
opus.type.contenttype	Keine	de_DE
opus.type.contenttype	None	en_EN
opus.affiliated	Schollmeyer, Dieter	-
opus.affiliated	Detert, Heiner	-
jgu.publisher.doi	10.1107/S1600536814002153	de
jgu.organisation.ror	https://ror.org/023b0x485	-
Appears in collections:	DFG-OA-Publizieren (2012 - 2017)

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