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pubmed-article:21202706rdf:typepubmed:Citationlld:pubmed
pubmed-article:21202706pubmed:issuePt 6lld:pubmed
pubmed-article:21202706pubmed:dateCreated2011-1-4lld:pubmed
pubmed-article:21202706pubmed:abstractTextThe title compound, C(10)H(8)BrN, was obtained by slow addition of sodium azide to 8-bromo-1-naphthoic acid, followed by addition of aqueous ammonia. The crude product was crystallized from petroleum ether to give pink crystals. Compared to other 1,8-disubstituted naphthalene compounds, this compound exhibits less strain between the 1 and 8 substituents. Additionally, the NH protons form both intra- and inter-molecular hydrogen bonds. The naphthalene units are arranged in a herring-bone stacking motif.lld:pubmed
pubmed-article:21202706pubmed:commentsCorrectionshttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:21202706pubmed:languageenglld:pubmed
pubmed-article:21202706pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:21202706pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:21202706pubmed:issn1600-5368lld:pubmed
pubmed-article:21202706pubmed:authorpubmed-author:SlawinAlexand...lld:pubmed
pubmed-article:21202706pubmed:authorpubmed-author:WoollinsJ...lld:pubmed
pubmed-article:21202706pubmed:authorpubmed-author:FullerAmy LALlld:pubmed
pubmed-article:21202706pubmed:authorpubmed-author:KnightFergus...lld:pubmed
pubmed-article:21202706pubmed:issnTypeElectroniclld:pubmed
pubmed-article:21202706pubmed:volume64lld:pubmed
pubmed-article:21202706pubmed:ownerNLMlld:pubmed
pubmed-article:21202706pubmed:authorsCompleteYlld:pubmed
pubmed-article:21202706pubmed:paginationo977lld:pubmed
pubmed-article:21202706pubmed:dateRevised2011-11-11lld:pubmed
pubmed-article:21202706pubmed:year2008lld:pubmed
pubmed-article:21202706pubmed:articleTitle8-Bromo-naphthalen-1-amine.lld:pubmed
pubmed-article:21202706pubmed:affiliationDepartment of Chemistry, University of St Andrews, St Andrews KY16 9ST, Scotland.lld:pubmed
pubmed-article:21202706pubmed:publicationTypeJournal Articlelld:pubmed