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pubmed-article:21202580rdf:typepubmed:Citationlld:pubmed
pubmed-article:21202580pubmed:issuePt 6lld:pubmed
pubmed-article:21202580pubmed:dateCreated2011-1-4lld:pubmed
pubmed-article:21202580pubmed:abstractTextThe title compound, C(16)H(13)IO(2)S, was prepared by the oxidation of 2-(4-iodo-phen-yl)-5-methyl-3-methyl-sulfanyl-1-benzofuran with 3-chloro-peroxy-benzoic acid. The 4-iodo-phenyl ring makes a dihedral angle of 37.97?(9)° with the plane of the benzofuran fragment, and the O atom and the methyl group of the methyl-sulfinyl substituent lie on opposite sides of this plane. The mol-ecular packing is stabilized by C-H?? inter-actions between H atoms on the 4-iodo-phenyl ring and the benzofuran rings, and by an I?O halogen bond of 3.252?(2)?Å with a nearly linear C-I?O angle of 163.06?(8)°. In addition, the stacked mol-ecules exhibit inversion-related S?O contacts [3.209?(2)?Å] involving the sulfinyl groups.lld:pubmed
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pubmed-article:21202580pubmed:languageenglld:pubmed
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pubmed-article:21202580pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:21202580pubmed:issn1600-5368lld:pubmed
pubmed-article:21202580pubmed:authorpubmed-author:SonByeng...lld:pubmed
pubmed-article:21202580pubmed:authorpubmed-author:ChoiHong...lld:pubmed
pubmed-article:21202580pubmed:authorpubmed-author:LeeUkUlld:pubmed
pubmed-article:21202580pubmed:authorpubmed-author:SeoPil JaPJlld:pubmed
pubmed-article:21202580pubmed:issnTypeElectroniclld:pubmed
pubmed-article:21202580pubmed:volume64lld:pubmed
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pubmed-article:21202580pubmed:authorsCompleteYlld:pubmed
pubmed-article:21202580pubmed:paginationo1061lld:pubmed
pubmed-article:21202580pubmed:dateRevised2011-11-11lld:pubmed
pubmed-article:21202580pubmed:year2008lld:pubmed
pubmed-article:21202580pubmed:articleTitle2-(4-Iodo-phen-yl)-5-methyl-3-methyl-sulfinyl-1-benzofuran.lld:pubmed
pubmed-article:21202580pubmed:publicationTypeJournal Articlelld:pubmed