<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>64(Pt 4)</volume><submitter>Niaz M</submitter><pubmed_abstract>In the crystal structure of the title compound, C(11)H(11)FO(2), the methine CH forms an intra-molecular hydrogen bond with the carboxyl- O atom. The mol-ecules form dimers through hydrogen bonding between carboxyl- groups. These dimers are linked to each other by C-H⋯O contacts between the benzene and carbonyl groups of adjoining mol-ecules. In addition, there are weak inter-molecular C-H⋯F contacts.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o733</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2960906</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>(E)-2-(2-Fluoro-benzyl-idene)butanoic acid.</pubmed_title><pmcid>PMC2960906</pmcid><pubmed_authors>Khan IU</pubmed_authors><pubmed_authors>Ali S</pubmed_authors><pubmed_authors>Zia-Ur-Rehman</pubmed_authors><pubmed_authors>Niaz M</pubmed_authors><pubmed_authors>Tahir MN</pubmed_authors></additional><is_claimable>false</is_claimable><name>(E)-2-(2-Fluoro-benzyl-idene)butanoic acid.</name><description>In the crystal structure of the title compound, C(11)H(11)FO(2), the methine CH forms an intra-molecular hydrogen bond with the carboxyl- O atom. The mol-ecules form dimers through hydrogen bonding between carboxyl- groups. These dimers are linked to each other by C-H⋯O contacts between the benzene and carbonyl groups of adjoining mol-ecules. In addition, there are weak inter-molecular C-H⋯F contacts.</description><dates><release>2008-01-01T00:00:00Z</release><publication>2008 Mar</publication><modification>2025-05-18T12:55:47.773Z</modification><creation>2025-05-18T12:55:47.773Z</creation></dates><accession>S-EPMC2960906</accession><cross_references><pubmed>21202123</pubmed><doi>10.1107/S1600536808007149</doi></cross_references></HashMap>