biostudies-literatureBairagi KMDurban University of TechnologyNational Research FoundationVisvesvaraya Technological University1130-1133https://www.ebi.ac.uk/biostudies/studies/S-EPMC6072987biostudies-literatureUnknown74(Pt 8)The title compounds, 2-iodo-benzamide, C7H6INO (I), and 2-iodo-N-phenyl-benzamide, C13H10INO (II), were both synthesized from 2-iodo-benzoic acid. In the crystal structure of (I), N-H⋯O and hydrogen bonds form two sets of closed rings, generating dimers and tetra-mers. These combine with C-I⋯π(ring) halogen bonds to form sheets of mol-ecules in the bc plane. For (II), N-H⋯O hydrogen bonds form chains along the a-axis direction, while inversion-related C-I⋯π(ring) contacts supported by C-H⋯π(ring) interactions generate sheets of mol-ecules along the ab diagonal.Acta crystallographica. Section E, Crystallographic communicationsStructural analysis of 2-iodo-benzamide and 2-iodo-N-phenyl-benzamide.PMC60729879199596807Kumar VBSNayak SKBhandary SVenugopala KNBairagi KMfalseStructural analysis of 2-iodo-benzamide and 2-iodo-N-phenyl-benzamide.The title compounds, 2-iodo-benzamide, C7H6INO (I), and 2-iodo-N-phenyl-benzamide, C13H10INO (II), were both synthesized from 2-iodo-benzoic acid. In the crystal structure of (I), N-H⋯O and hydrogen bonds form two sets of closed rings, generating dimers and tetra-mers. These combine with C-I⋯π(ring) halogen bonds to form sheets of mol-ecules in the bc plane. For (II), N-H⋯O hydrogen bonds form chains along the a-axis direction, while inversion-related C-I⋯π(ring) contacts supported by C-H⋯π(ring) interactions generate sheets of mol-ecules along the ab diagonal.2018-01-01T00:00:00Z2018 Aug2024-02-16T02:55:48.546Z2019-03-26T23:51:31ZS-EPMC60729873011657710.1107/S2056989018010162