2154-71-4

Basic information

• Product Name: BIS(TRIFLUOROMETHYL)NITROXIDE
• Synonyms: BIS(TRIFLUOROMETHYL)NITROXIDE
• CAS NO: 2154-71-4
• Molecular Formula: C₂F₆NO
• Molecular Weight: 168.02
• Mol File: 2154-71-4.mol
• Article Data: 2

Chemical Properties

• Melting Point: -69.9°C
• Boiling Point: -25°C
• Appearance: /
• CAS DataBase Reference: BIS(TRIFLUOROMETHYL)NITROXIDE(CAS DataBase Reference)
• NIST Chemistry Reference: BIS(TRIFLUOROMETHYL)NITROXIDE(2154-71-4)
• EPA Substance Registry System: BIS(TRIFLUOROMETHYL)NITROXIDE(2154-71-4)

Safety Data

• Statements: 23/24/25
• Safety Statements: 23-36/37/39-38
• RIDADR: 3162
• Hazardous Substances Data: 2154-71-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C2F6NO/c3-1(4,5)9(10)2(6,7)8

Upstream product

• 383-73-3 bis(trifluoroacetyl)peroxide 
• 24163-39-1 sodium 2-nitropropane 
• 62487-45-0 tris(pentafluorophenyl)-bis{bis(trifluoromethyl)aminooxy}stiborane 

Downstream Products

• 6998-35-2 Perfluor-<1,2-bis-(N,N-dimethylnitroxy)-propan 
• 7309-82-2 perfluoropyruvic acid fluoride 
• 19555-07-8 Decafluorobenzil 
• 25552-53-8 C₁₀F₂₂N₂O₂ 
• 39128-55-7 C₁₂H₄F₁₂N₂O₄ 
• 22264-95-5 benzoyl bistrifluormethylnitroxide 
• 6141-73-7 O-Benzyl-N,N-bis-(trifluormethyl)-hydroxylamin 
• 39128-54-6 C₁₀H₇F₆NO₂ 
• 359-63-7 N,N-bis(trifluoromethyl)hydroxylamine 
• 74770-43-7 perfluoro(2,5-dimethyl-4-oxa-3,5-diazahex-2-ene) 
• 74770-46-0 azoxy 
• 684-16-2 Hexafluoroacetone 
• 613-90-1 benzoyl cyanide 
• 6141-72-6 perfluoro(2,4-dimethyl-3-oxa-2,4-diazapentane) 

Relevant articles and documents

GENERATION OF 15N LABELLED BIS(POLYFLUOROALKYL)NITROXIDES AND THEIR HYDROGEN-ABSTRACTION REACTIONS WITH ALKANES, ALKYLBENZENES AND ALDEHYDES

Blue solutions containing 15N labelled bis(polyfluoroalkyl) nitroxides and spin traps, polyfluoronitrosoalkanes, were conveniently made from the reactions of Na15NO2 with polyfluoro-compounds, (RFCO2), RFI and RFSO2Br in F113.It has been found that the nitroxides effected fast H-abstraction from alkanes, alkylbenzenes, aldehydes and the radicals derived from the substrates were in turn effectively trapped by RF15NO to give 15N labelled spin adducts detectable by ESR.The bigger aN(15N) values as well as much simpler splittings of both the nitroxides and the spin adducts have made the kinetic studies of the H-abstraction and other radical reactions quite feasible.