CAS 4316-58-9
:Tris(4-bromophényl)amine
- 4,4',4"-Tribromotriphenylamine
- 4,4′,4′′-Tribromotriphenylamine
- 4-Bromo-N,N-bis(4-bromophenyl)benzenamine
- 4-bromo-N,N-bis(4-bromophenyl)aniline
- Benzenamine, 4-bromo-N,N-bis(4-bromophenyl)-
- N,N-Bis(4-bromophenyl)-4-bromoaniline
- N,N-Diphenyl-4,4′,4′′-tribromoaniline
- NSC 86666
- Tri(4-bromophenyl) amine
- Tri(p-bromophenyl)amine
- Triphenylamine, 4,4′,4′′-tribromo-
- Tris(p-bromophenyl)amine
- Voir plus de synonymes
Tris(4-bromophenyl)amine
CAS :Formule :C18H12Br3NDegré de pureté :>98.0%(GC)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :482.01Tris(4-bromophenyl)amine, 98%
CAS :Tris(4-bromophenyl)amine was used in the synthesis of porous luminescent covalent--organic polymers (COPs) This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa
Formule :C18H12Br3NDegré de pureté :98%Couleur et forme :White to pale green, PowderMasse moléculaire :482.01Tris(4-bromophenyl)amine
CAS :Formule :C18H12Br3NDegré de pureté :97%Couleur et forme :SolidMasse moléculaire :482.0066Tris(4-bromophenyl)amine
CAS :Tris(4-bromophenyl)amineFormule :C18H12Br3NDegré de pureté :98%Couleur et forme : off-white solidMasse moléculaire :482.00658g/molTris(4-bromophenyl)amine (purified by sublimation)
CAS :Formule :C18H12Br3NDegré de pureté :>99.0%(GC)Couleur et forme :White to Almost white powder to crystalMasse moléculaire :482.01Tris(4-bromophenyl)amine
CAS :Degré de pureté :97%Couleur et forme :SolidMasse moléculaire :482.01300048828125Tris(4-bromophenyl)amine
CAS :Tris(4-bromophenyl)amine is a chemical compound that is used as an intermediate in the synthesis of other compounds. It has been studied for its electrochemical properties, which include its stability and ability to react with ethyl diazoacetate. The reaction mechanism of tris(4-bromophenyl)amine has been studied using electrochemical techniques, including kinetic and spectroscopic studies. Tris(4-bromophenyl)amine reacts with acid to produce nitrite ions and bromine water, which can then react with ethyl diazoacetate to produce aryl diazonium salts such as 3-nitrophenol. This process can be repeated multiple times to form aryl diazonium salts such as 6-nitrophenol or 5-nitrophenol. The electron reduction potential of tris(4-bromophenyl)amine is low enough that it can be easily oxid
Formule :C18H12Br3NDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :482.01 g/mol





