<HashMap><database>biostudies-literature</database><scores><citationCount>0</citationCount><reanalysisCount>0</reanalysisCount><viewCount>56</viewCount><searchCount>0</searchCount></scores><additional><omics_type>Unknown</omics_type><volume>67(Pt 10)</volume><submitter>Fun HK</submitter><pubmed_abstract>In the title compound, C(16)H(15)NOS, the thia-zolidine ring, which is essentially planar [maximum deviation = 0.071?(2)?Å], makes dihedral angles of 88.01?(8) and 87.21?(8)° with the terminal phenyl rings. The dihedral angle between the phenyl rings is 49.45?(5)°. In the crystal, mol-ecules are linked by a weak inter-molecular C-H?O hydrogen bond, forming a supra-molecular chain along the b axis. Furthermore, the crystal packing is stabilized by a weak C-H?? inter-action.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o2706</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3201390</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>3-Benzyl-2-phenyl-1,3-thia-zolidin-4-one.</pubmed_title><pmcid>PMC3201390</pmcid><pubmed_authors>Ponnuswamy A</pubmed_authors><pubmed_authors>Fun HK</pubmed_authors><pubmed_authors>Jagatheesan R</pubmed_authors><pubmed_authors>Hemamalini M</pubmed_authors><pubmed_authors>Shanmugavelan P</pubmed_authors><view_count>56</view_count></additional><is_claimable>false</is_claimable><name>3-Benzyl-2-phenyl-1,3-thia-zolidin-4-one.</name><description>In the title compound, C(16)H(15)NOS, the thia-zolidine ring, which is essentially planar [maximum deviation = 0.071?(2)?Å], makes dihedral angles of 88.01?(8) and 87.21?(8)° with the terminal phenyl rings. The dihedral angle between the phenyl rings is 49.45?(5)°. In the crystal, mol-ecules are linked by a weak inter-molecular C-H?O hydrogen bond, forming a supra-molecular chain along the b axis. Furthermore, the crystal packing is stabilized by a weak C-H?? inter-action.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Oct</publication><modification>2021-02-21T03:18:32Z</modification><creation>2019-03-26T23:59:30Z</creation></dates><accession>S-EPMC3201390</accession><cross_references><pubmed>22064819</pubmed><doi>10.1107/S1600536811037706</doi></cross_references></HashMap>