<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>67(Pt 9)</volume><submitter>Ennajih H</submitter><pubmed_abstract>In the title compound, C(10)H(7)NO(2)S, the dihedral angle between the benzimidazole and malonaldehyde group is 1.41 (2)°. An intra-molecular hydrogen bond is formed between the NH group and one of the adjacent carbonyl O atoms. In addition, the NH group forms an inter-molecular hydrogen bond to a symmetry equivalent of this carbonyl O atom, connecting the mol-ecules into centrosymmetric dimers. The structure also contains C-H⋯O inter-molecular inter-actions.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o2260</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3200844</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>2-(3H-1,3-Benzothia-zol-2-yl-idene)-propane-dial.</pubmed_title><pmcid>PMC3200844</pmcid><pubmed_authors>Massip S</pubmed_authors><pubmed_authors>Bouhfid R</pubmed_authors><pubmed_authors>Ennajih H</pubmed_authors><pubmed_authors>Essassi el M</pubmed_authors><pubmed_authors>Leger JM</pubmed_authors></additional><is_claimable>false</is_claimable><name>2-(3H-1,3-Benzothia-zol-2-yl-idene)-propane-dial.</name><description>In the title compound, C(10)H(7)NO(2)S, the dihedral angle between the benzimidazole and malonaldehyde group is 1.41 (2)°. An intra-molecular hydrogen bond is formed between the NH group and one of the adjacent carbonyl O atoms. In addition, the NH group forms an inter-molecular hydrogen bond to a symmetry equivalent of this carbonyl O atom, connecting the mol-ecules into centrosymmetric dimers. The structure also contains C-H⋯O inter-molecular inter-actions.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Sep</publication><modification>2025-04-04T08:06:23.739Z</modification><creation>2019-03-26T23:59:26Z</creation></dates><accession>S-EPMC3200844</accession><cross_references><pubmed>22065714</pubmed><doi>10.1107/S1600536811030248</doi></cross_references></HashMap>