<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>71(Pt 11)</volume><submitter>El-Hiti GA</submitter><pubmed_abstract>In the title compound, C12H14N2S, the cyclo-hexane ring adopts a chair conformation with the exocyclic C-C bond in an equatorial orientation. The mean plane through the cyclo-hexane ring (all atoms) is twisted from the thia-zolo-pyridine ring system (r.m.s. deviation = 0.013 Å) by 39.57 (6)°. In the crystal, mol-ecules form (100) sheets, although there are no specific directional inter-actions between them. The crystal stucture was refined as a two-component perfect twin.</pubmed_abstract><journal>Acta crystallographica. Section E, Crystallographic communications</journal><pagination>o866</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4645017</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Crystal structure of 2-cyclo-hexyl-1,3-thia-zolo[4,5-b]pyridine.</pubmed_title><pmcid>PMC4645017</pmcid><pubmed_authors>Hegazy AS</pubmed_authors><pubmed_authors>El-Hiti GA</pubmed_authors><pubmed_authors>Ajarim MD</pubmed_authors><pubmed_authors>Kariuki BM</pubmed_authors><pubmed_authors>Smith K</pubmed_authors></additional><is_claimable>false</is_claimable><name>Crystal structure of 2-cyclo-hexyl-1,3-thia-zolo[4,5-b]pyridine.</name><description>In the title compound, C12H14N2S, the cyclo-hexane ring adopts a chair conformation with the exocyclic C-C bond in an equatorial orientation. The mean plane through the cyclo-hexane ring (all atoms) is twisted from the thia-zolo-pyridine ring system (r.m.s. deviation = 0.013 Å) by 39.57 (6)°. In the crystal, mol-ecules form (100) sheets, although there are no specific directional inter-actions between them. The crystal stucture was refined as a two-component perfect twin.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Nov</publication><modification>2025-04-18T23:09:59.068Z</modification><creation>2019-03-27T02:01:57Z</creation></dates><accession>S-EPMC4645017</accession><cross_references><pubmed>26594568</pubmed><doi>10.1107/S2056989015019106</doi></cross_references></HashMap>