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

General Description

1,2,3,4,5-pentafluoro-6-[(Z)-(pentafluorophenyl)-NNO-azoxy]benzene is a chemical compound that belongs to the class of azo compounds. It is characterized by its distinctive structure which consists of a benzene ring with six fluorine atoms and a pentafluorophenyl group connected to it. The compound also contains an azoxy group, denoted as NNO, which is attached to the pentafluorophenyl group in a Z configuration. This chemical is mainly used in the field of organic synthesis and has potential applications in the manufacturing of dyes, pigments, and other organic compounds due to its unique molecular structure and reactivity. Overall, 1,2,3,4,5-pentafluoro-6-[(Z)-(pentafluorophenyl)-NNO-azoxy]benzene is a specialized compound with interesting properties that make it a valuable building block in organic chemistry.

Upstream product

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

Downstream Products

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

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.