3008-32-0 Usage
Chemical structure
A perfluorinated compound with multiple repeating phenyl rings and fluorine atoms attached.
Stability
Highly stable and inert due to the presence of fluorine atoms.
Synthesis
Used as a building block in the synthesis of advanced materials and polymers.
Applications
Commonly used in various electronic and optical applications.
Physical properties
Perfluorotriphenylamine has unique chemical and physical properties that make it valuable in the field of materials science and technology.
Chemical properties
The compound is highly stable and resistant to chemical reactions due to the presence of fluorine atoms.
Molecular weight
Approximately 649.43 g/mol
Appearance
Perfluorotriphenylamine is typically a colorless or white solid.
Solubility
It is insoluble in water but soluble in organic solvents such as chloroform and acetone.
Melting point
The melting point of perfluorotriphenylamine is around 300°C.
Boiling point
The boiling point of perfluorotriphenylamine is not well-defined due to its high stability and resistance to decomposition.
Density
The density of perfluorotriphenylamine is approximately 1.7 g/cm3.
Hazards
Perfluorotriphenylamine is considered non-toxic and non-flammable, but it should be handled with care due to its potential for environmental contamination.
Environmental impact
Perfluorinated compounds, including perfluorotriphenylamine, have been found to be persistent in the environment and can accumulate in the food chain, posing potential risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 3008-32-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,0,0 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3008-32:
(6*3)+(5*0)+(4*0)+(3*8)+(2*3)+(1*2)=50
50 % 10 = 0
So 3008-32-0 is a valid CAS Registry Number.
3008-32-0Relevant articles and documents
Formation of perfluorinated polyphenylenes by multiple pentafluorophenylation using C6F5Si(CH3) 3
Nishida, Masakazu,Hayakawa, Yoshio,Ono, Taizo
experimental part, p. 1314 - 1321 (2011/02/22)
Pentafluorophenylation of perfluoroarenes with C6F 5Si(CH3)3 was investigated by using NMR and MALDI-TOF-MS techniques. Successive multiple pentafluorophenylation easily occurred not only on the para-position but also on the ortho-positions to provide perfluorinated p-phenylene and m-phenylene compounds. The perfluoroarenes having electron-withdrawing substituents provided oligo- to poly-(phenylene)s depending on the added amounts of C6F 5Si(CH3)3, while the perfluoroarenes having electron-donor substituents gave H(C6F4)nF polymers produced from C6F5H, which was the decomposed product of C6F5Si(CH3)3.
REACTION OF AROMATIC COMPOUNDS WITH NUCLEOPHILIC REAGENTS IN LIQUID AMMONIA IV.* THE NUCLEOPHILIC AND PROTOPHILIC ACTIVITY OF METHOXIDE AND HYDROXIDE IONS IN REACTIONS WITH POLYFLUORINATED AROMATIC COMPOUNDS
Shtark, A. A.,Chuikova, T. V.,Shteingarts, V. D.
, p. 960 - 967 (2007/10/02)
In the reaction of polyfluorinated derivatives of benzene with potassium methoxide in liquid ammonia a fluorine atom is substituted by a methoxy group.With potassium hydroxide reactions involving removal of a proton from a ring carbon atom take place preferentially.The possibility of polyfluoroarylation and methylation catalyzed by potassium hydroxide in polyfluorinated aromatic compounds, based on capture of the polyflurinated aryl anion by the electrophile, was demonstrated.
