<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>71(Pt 11)</volume><submitter>Chandra Kumar K</submitter><pubmed_abstract>In the title compound, C15H15FN2OS, the dihedral angle between the planes of the benzo-thio-phene ring system and the fluoro-benzene ring is 3.74 (14)°. The six-membered ring of the benzo-thio-phene moiety adopts a half-chair conformation. The mol-ecular conformation is consolidated by intra-molecular N-H⋯F and N-H⋯O hydrogen bonds. In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds, generating C(6) [001] chains.</pubmed_abstract><journal>Acta crystallographica. Section E, Crystallographic communications</journal><pagination>o807-8</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4645083</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Crystal structure of 2-amino-N-(2-fluoro-phen-yl)-4,5,6,7-tetra-hydro-1-benzo-thio-phene-3-carboxamide.</pubmed_title><pmcid>PMC4645083</pmcid><pubmed_authors>Chandra</pubmed_authors><pubmed_authors>Rajesh BM</pubmed_authors><pubmed_authors>Chandra Kumar K</pubmed_authors><pubmed_authors>Madhura TK</pubmed_authors><pubmed_authors>Umesh V</pubmed_authors></additional><is_claimable>false</is_claimable><name>Crystal structure of 2-amino-N-(2-fluoro-phen-yl)-4,5,6,7-tetra-hydro-1-benzo-thio-phene-3-carboxamide.</name><description>In the title compound, C15H15FN2OS, the dihedral angle between the planes of the benzo-thio-phene ring system and the fluoro-benzene ring is 3.74 (14)°. The six-membered ring of the benzo-thio-phene moiety adopts a half-chair conformation. The mol-ecular conformation is consolidated by intra-molecular N-H⋯F and N-H⋯O hydrogen bonds. In the crystal, mol-ecules are linked by N-H⋯O hydrogen bonds, generating C(6) [001] chains.</description><dates><release>2015-01-01T00:00:00Z</release><publication>2015 Nov</publication><modification>2025-04-04T10:50:39.209Z</modification><creation>2019-03-27T02:01:57Z</creation></dates><accession>S-EPMC4645083</accession><cross_references><pubmed>26594537</pubmed><doi>10.1107/S2056989015018022</doi></cross_references></HashMap>