Source:http://linkedlifedata.com/resource/pubmed/id/21202706
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| Predicate | Object |
|---|---|
| rdf:type | |
| pubmed:issue |
Pt 6
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| pubmed:dateCreated |
2011-1-4
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| pubmed:abstractText |
The 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.
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| pubmed:commentsCorrections | |
| pubmed:language |
eng
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| pubmed:journal | |
| pubmed:status |
PubMed-not-MEDLINE
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| pubmed:issn |
1600-5368
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| pubmed:author | |
| pubmed:issnType |
Electronic
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| pubmed:volume |
64
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| pubmed:owner |
NLM
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| pubmed:authorsComplete |
Y
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| pubmed:pagination |
o977
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| pubmed:dateRevised |
2011-11-11
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| pubmed:year |
2008
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| pubmed:articleTitle |
8-Bromo-naphthalen-1-amine.
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| pubmed:affiliation |
Department of Chemistry, University of St Andrews, St Andrews KY16 9ST, Scotland.
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| pubmed:publicationType |
Journal Article
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