Document
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Canadian Journal of Chemistry
type: Journal
type: Generically Dependent Continuant
type: Entity
type: Collection
type: Continuant
type: Thing
publication venue for: Chemical oxidation of fluoroanilines to fluoroazobenzenes and fluorophenazines with potassium ferricyanide and potassium hydroxide
type: Periodical
type: Document
type: Information Content Entity

Generically Dependent Continuant
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RDF description of Chemical oxidation of fluoroanilines to fluoroazobenzenes and fluorophenazines with potassium ferricyanide and potassium hydroxide - http://orbis.uaslp.mx/vivo/individual/scopus1375
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date: 2026-08-28T02:11:35
publisher: vivo
type: Document

Article
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Information Content Entity
type: Class

Chemical oxidation of fluoroanilines to fluoroazobenzenes and fluorophenazines with potassium ferricyanide and potassium hydroxide
type: Entity
issue: 12
type: Information Content Entity
freetext keyword: Fluoroanilines; Fluoroazobenzenes; Fluorophenazines; Oxidation Benzene; Cyanides; Oxidation; Potassium compounds; Reaction kinetics; Chemical oxidation; Fluoroanilines; Fluoroazobenzenes; Potassium hydroxide; Amines; aniline derivative; azobenzene derivative; fluoroaniline derivative; fluoroazobenzene derivative; fluorophenazine derivative; phenazine derivative; potassium ferricyanide; potassium hydroxide; unclassified drug; article; oxidation; phase transition; reaction analysis; solubility
most specific type: Document
type: Document
type: Thing
volume: 82
most specific type: Article
related by: authorship 8230
page end: 1715
chemicalscas: potassium ferricyanide, 13746-66-2; potassium hydroxide, 1310-58-3
related by: authorship 8228
crisid: 1376
type: Generically Dependent Continuant
related by: authorship 8231
date time value: article date 1376
doi: 10.1139/v04-150
estado: published
e iscopus: 2-s2.0-20144383973
has publication venue: Canadian Journal of Chemistry
abstract: The oxidation of several fluoroanilines with potassium ferricyanide and potassium hydroxide is described. In this oxidation, the major products are fluoroazobenzenes. In the case of 2-fluoro-substituted anilines, heterocyclic fluorophenazines were obtained in low to moderate yields. The optimal conditions for the reaction and the mechanism are presented. © 2004 NRC Canada.
origen: scopus
page start: 1712
type: Article
type: Continuant
related by: authorship 8229