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Authordc.contributor.authorBravo, Héctor R. 
Authordc.contributor.authorNiemeyer, Hermann M. 
Admission datedc.date.accessioned2018-12-20T15:04:11Z
Available datedc.date.available2018-12-20T15:04:11Z
Publication datedc.date.issued1991
Cita de ítemdc.identifier.citationHeterocycles, Volumen 32, Issue 9, 2018, Pages 1687-1691
Identifierdc.identifier.issn03855414
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/157478
Abstractdc.description.abstractKinetic and product studies indicate that the title compound decomposes in aqueous solutions to give 5-nitro-2-aminophenol with the intermediacy of N-(2-hydroxy-4-nitrophenyl)carbamic acid. © 1991.
Lenguagedc.language.isoen
Type of licensedc.rightsAttribution-NonCommercial-NoDerivs 3.0 Chile
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/
Sourcedc.sourceHeterocycles
Keywordsdc.subjectAnalytical Chemistry
Keywordsdc.subjectPharmacology
Keywordsdc.subjectOrganic Chemistry
Títulodc.titleDecomposition of 7-nitro-2,4-dihydroxy-1,4-benzoxazin-3-one in aqueous solutions
Document typedc.typeArtículo de revista
Catalogueruchile.catalogadorSCOPUS
Indexationuchile.indexArtículo de publicación SCOPUS
uchile.cosechauchile.cosechaSI


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Attribution-NonCommercial-NoDerivs 3.0 Chile
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivs 3.0 Chile