<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>66(Pt 5)</volume><submitter>Choi HD</submitter><pubmed_abstract>In the title compound, C(16)H(12)FIO(2)S, the 4-fluoro-phenyl ring is rotated slightly out of the benzofuran plane, as indicated by the dihedral angle of 4.48 (5)°. In the crystal structure, pairs of I⋯O halogen bonds [I⋯O = 3.123 (1) Å] link the mol-ecules into centrosymmetric dimers. These dimers are further linked via aromatic π-π inter-actions between the benzene and 4-fluoro-phenyl rings of neighbouring mol-ecules [centroid-centroid distance = 3.620 (3) Å].</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o1043</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2979084</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>3-Ethyl-sulfinyl-2-(4-fluoro-phen-yl)-5-iodo-1-benzofuran.</pubmed_title><pmcid>PMC2979084</pmcid><pubmed_authors>Son BW</pubmed_authors><pubmed_authors>Choi HD</pubmed_authors><pubmed_authors>Seo PJ</pubmed_authors><pubmed_authors>Lee U</pubmed_authors></additional><is_claimable>false</is_claimable><name>3-Ethyl-sulfinyl-2-(4-fluoro-phen-yl)-5-iodo-1-benzofuran.</name><description>In the title compound, C(16)H(12)FIO(2)S, the 4-fluoro-phenyl ring is rotated slightly out of the benzofuran plane, as indicated by the dihedral angle of 4.48 (5)°. In the crystal structure, pairs of I⋯O halogen bonds [I⋯O = 3.123 (1) Å] link the mol-ecules into centrosymmetric dimers. These dimers are further linked via aromatic π-π inter-actions between the benzene and 4-fluoro-phenyl rings of neighbouring mol-ecules [centroid-centroid distance = 3.620 (3) Å].</description><dates><release>2010-01-01T00:00:00Z</release><publication>2010 Apr</publication><modification>2025-04-04T14:42:20.191Z</modification><creation>2019-03-27T00:00:22Z</creation></dates><accession>S-EPMC2979084</accession><cross_references><pubmed>21579104</pubmed><doi>10.1107/S1600536810012717</doi></cross_references></HashMap>