Molecular Formula | C10H12N2 |
Molar Mass | 160.22 |
Density | 1.055±0.06 g/cm3(Predicted) |
Boling Point | 173-174 °C(Press: 10 Torr) |
Flash Point | 142.026°C |
Vapor Presure | 0.001mmHg at 25°C |
pKa | 3.63±0.10(Predicted) |
Storage Condition | under inert gas (nitrogen or Argon) at 2–8 °C |
Sensitive | IRRITANT |
Refractive Index | 1.556 |
MDL | MFCD09909912 |
introduction | 2-(4-aminophenyl)-2-methylpropionitrile is both cyanide and aromatic primary amine, so it has multiple reaction sites and is an important pharmaceutical and chemical intermediate. |
application | 2-(4-aminophenyl)-2-methylpropiononitrile can be used as an intermediate in organic synthesis and a pharmaceutical intermediate, and can be mainly used in laboratory research and development and chemical production. |
use | 2-(4-aminophenyl)-2-methylpropionitrile is used as an organic and pharmaceutical intermediate. |
preparation | 2-(4-nitrophenyl)-2-methylpropionitrile is used as the starting material for hydrogenation reduction reaction, Raney nickel is used as the catalyst to prepare 2-(4-aminophenyl)-2-methylpropionitrile, or 2-(4-chlorophenyl)-2-methylpropiononitrile is used as the starting material to prepare 2-(4-aminophenyl)-2-methylpropiononitrile through ammonolysis reaction. The synthesis reaction formula is as follows: |