1800-29-9

Basic information

• Product Name: 1,2,3,4,5-pentafluoro-6-[(Z)-(pentafluorophenyl)-NNO-azoxy]benzene
• Synonyms: Diazene, bis(pentafluorophenyl)-, 1-oxide
• CAS NO: 1800-29-9
• Molecular Formula: C₁₂F₁₀N₂O
• Molecular Weight: 378.1252
• Mol File: 1800-29-9.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 350.5°C at 760 mmHg
• Flash Point: 165.8°C
• Density: 1.79g/cm³
• Vapor Pressure: 8.86E-05mmHg at 25°C
• Refractive Index: 1.475
• CAS DataBase Reference: 1,2,3,4,5-pentafluoro-6-[(Z)-(pentafluorophenyl)-NNO-azoxy]benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4,5-pentafluoro-6-[(Z)-(pentafluorophenyl)-NNO-azoxy]benzene(1800-29-9)
• EPA Substance Registry System: 1,2,3,4,5-pentafluoro-6-[(Z)-(pentafluorophenyl)-NNO-azoxy]benzene(1800-29-9)

Safety Data

• Hazardous Substances Data: 1800-29-9(Hazardous Substances Data)

Usage

Chemical class

Azo compounds

Structure

Benzene ring with six fluorine atoms, pentafluorophenyl group, and an azoxy (NNO) group in a Z configuration

Fluorine atoms

6

Pentafluorophenyl group

Connected to the benzene ring

Azoxy group

NNO, attached to the pentafluorophenyl group in a Z configuration

Applications

Organic synthesis, manufacturing of dyes, pigments, and other organic compounds

Unique molecular structure

Contributes to its reactivity and potential applications

Reactivity

Specialized compound with interesting properties for use in organic chemistry

Field of use

Mainly in the field of organic synthesis

Potential applications

Building block in organic chemistry due to its distinctive structure and reactivity

Upstream product

• 1423-13-8 pentafluoronitrosobenzene 
• 771-60-8 2,3,4,5,6-pentafluoroaniline 
• 880-78-4 pentafluoronitrobenzen 
• 105608-97-7 N-pentafluorophenylhydroxylamine 
• 7722-84-1 dihydrogen peroxide 
• 2285-06-5 bis(pentafluorophenyl)diazene 

Downstream Products

• 344-07-0 1-chloro-2,3,4,5,6-pentafluorobenzene 
• 970-16-1 4-hydroxy-2,3,5,6-tetrafluoro-4'-dimethylaminoazobenzene 
• 2285-06-5 (E)-1,2-bis(pentafluorophenyl)diazene 
• 2379-19-3 N,N'-bis(pentafluorophenyl)-hydrazine 
• 2285-06-5 bis(pentafluorophenyl)diazene 
• 2787-85-1 4,4'-CH₃O-C₆F₄N(O)NC₆F₄OCH₃ 

Relevant articles and documents

HIGH PERFORMANCE LIQUID CHROMATOGRAPHY OF SOME N-PENTAFLUOROPHENYL DERIVATIVES

Performic acid oxidation of pentafluorophenylaniline was examined.High-performance liquid chromatography (HPLC) was applied to the separation and analysis of pentafluoronitrosobenzene, decafluoroazoxybenzene, pentafluorophenylhydroxylamine and pentafluoroaniline.Oxidation of the hydroxylamine occurred during elution.The identity and purity of the chromatographic peaks were established by an Evaluation programme.

N-(POLYFLUOROARYL)-HIDROXYLAMINES. SYNTHESIS AND PROPERTIES

Fluorine-containing N-arylhydroxylamines have been obtained by the reaction of hydroxylamine or its N- and O-derivatives on polyfluorinated benzenes and pentafluoropyridine.The influence of fluorine atoms on the reactivity of hydroxylamino group has been investigated.The reaction of N-polyflouroarylhydroxylamines with aldehydes has been shown not to occur, whereas their reaction with nitrosobenzenes leads to azoxybenzenes and with Lewis acids leads to corresponding nitrosobenzenes, azoxybenzenes and anilines.The action of acids on 2,3,5,6-tetrafluorophenylhydroxylamine leads to the acid-catalyzed rearrangement of the latter into 4-amino-2,3,5,6-tetrafluorophenol.C,N-Diarylnitrones have been obtained by the oxidation with MnO2 of fluorine-containing arylhydroxylamines possessing the CH-fragment in an α-position.