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| CAS number | 2205054-16-4 |
| Molecular formula | |
| Product name | 4',1'']terphenyl-4-yl-amine |
| Molecular Structure |
4-terphenyl-4-yl-amine is a versatile chemical compound with a wide range of applications in the chemical and pharmaceutical industries. It is an amine derivative of 4-terphenyl, a common aromatic hydrocarbon.
4-terphenyl-4-yl-amine is a colorless solid at room temperature. It is soluble in common organic solvents such as ethanol, methanol, and acetone. It has a molecular weight of 259.34 g/mol and a melting point of 109-110 °C.
4-terphenyl-4-yl-amine is used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. It is also used as a reagent in organic chemistry research and as a catalyst in chemical reactions.
The most common uses of 4-terphenyl-4-yl-amine are in pharmaceuticals. It is used to synthesize amide-containing drugs, such as amantadine and memantine, which are used to treat Parkinson's disease and Alzheimer's disease, respectively. It is also used to synthesize a variety of other drug compounds including antifungal agents, anxiolytic drugs, and antipsychotics.
In addition, 4-terphenyl-4-yl-amine is used as a reagent in organic synthesis and as a catalyst in chemical reactions. It can be used to catalyze the Friedel-Crafts reaction, the Mannich reaction, and the Curtius reaction.
4-terphenyl-4-yl-amine is also used as an intermediate in the synthesis of other organic compounds, including dyes, pigments, and fragrances. It is also used in the synthesis of certain agricultural chemicals and pesticides.
4-terphenyl-4-yl-amine has a wide range of applications in the chemical and pharmaceutical industries due to its versatility and reactivity. It is an important intermediate in the synthesis of many pharmaceuticals and other organic compounds, and it is also used as a catalyst in various chemical reactions. It is a colorless solid at room temperature and is soluble in common organic solvents.
