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dc.contributor.authorDolzhenko, Anton
dc.contributor.authorTan, G.
dc.contributor.authorKoh, L.
dc.contributor.authorDolzhenko, A.
dc.contributor.authorChui, W.
dc.date.accessioned2017-01-30T12:02:21Z
dc.date.available2017-01-30T12:02:21Z
dc.date.created2011-04-28T20:01:31Z
dc.date.issued2011
dc.identifier.citationDolzhenko, Anton and Tan, Geok and Koh, Lip and Dolzhenko, Anna and Chui, Wai. 2011. 7-(4-Fluorobenzylamino)-2-phenyl-1,2,4-triazolo[1,5-a][1,3,5]triazin-5-amine methanol disolvate. Acta Crystallographica Section E - Structure Reports Online 67 (5): pp. o1183-o1184.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/17517
dc.identifier.doi10.1107/S1600536811014176
dc.description.abstract

THe 1,2,4-triazolo[1,5-a][1,3,5]triazine system in the title compound, C17H14FN7.2CH3OH, is essentially planar, with an r.m.s. deviation of 0.0215 A. The attached phenyl ring lies almost in the mean plane of the heterocyclic core [dihedral angle = 3.56 (4)deg]. In the crystal, centrosymmetric inversion dimers connected via intermolecular N=H...N hydrogen bonds between H atom of the primary amino group and the triazine N atom [R22(8) graph-set motif] form sheets parallel to (010). A second set of dimers connected via N=H...F hydrogen bonds between the other H atom of the primaryamino group and the F atom forms an R22(24) graph-set motif linking the sheets. Methanol solvent molecules are packed in channels running along the [010] direction.

dc.publisherBlackwell Munksgaard
dc.subject5-azapurines
dc.subjectsolvate
dc.subjecttriazines. triazoles
dc.subjectcrystallography
dc.title7-(4-Fluorobenzylamino)-2-phenyl-1,2,4-triazolo[1,5-a][1,3,5]triazin-5-amine methanol disolvate
dc.typeJournal Article
dcterms.source.volume67
dcterms.source.number5
dcterms.source.startPageo1183
dcterms.source.endPageo1184
dcterms.source.issn16005368
dcterms.source.titleActa Crystallographica Section E - Structure Reports Online
curtin.note

This open access article is distributed under the terms of the Creative Commons Attribution Licence http://creativecommons.org/licenses/by/2.0/uk/legalcode, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

curtin.departmentSchool of Pharmacy
curtin.accessStatusOpen access


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