CAS 827-23-6
:2,4-Dibromo-6-nitroaniline
- Benzenamine, 2,4-dibromo-6-nitro-
- 2,4-Dibromo-6-nitrobenzenamine
2,4-Dibromo-6-nitroaniline
CAS :Formule :C6H4Br2N2O2Degré de pureté :>98.0%(GC)Couleur et forme :Light yellow to Yellow to Orange powder to crystalMasse moléculaire :295.922,4-Dibromo-6-nitroaniline, 99%
CAS :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 Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci
Formule :C6H4Br2N2O2Degré de pureté :99%Couleur et forme :Dark yellow to yellow, Crystals or powder or crystalline powderMasse moléculaire :295.92Benzenamine, 2,4-dibromo-6-nitro-
CAS :Formule :C6H4Br2N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :295.91622,4-Dibromo-6-nitroaniline
CAS :2,4-Dibromo-6-nitroanilineDegré de pureté :98%Masse moléculaire :295.92g/mol2,4-Dibromo-6-nitroaniline
CAS :Formule :C6H4Br2N2O2Degré de pureté :98%Couleur et forme :SolidMasse moléculaire :295.9182,4-Dibromo-6-nitroaniline
CAS :2,4-Dibromo-6-nitroaniline is a nitro compound that has been used in the production of dyes. It is also used as a component in the synthesis of other organic compounds. 2,4-Dibromo-6-nitroaniline can be produced by electrolysis of an acid solution containing radical cations and benzene. The radical cations are formed by proton transfer from the acid to the benzene, followed by electron transfer from benzene to the electrode. This process results in the formation of nitro groups on the benzene ring, which undergoes oxidation to form 2,4-dibromo-6-nitroaniline. The cyclic voltammetry shows that this process occurs via two pathways: one with a fast rate and one with a slow rate. The mechanism for this reaction is not yet known.
Formule :C6H4Br2N2O2Degré de pureté :Min. 95%Masse moléculaire :295.92 g/mol





