57103-13-6

Molecular Weight：299.40900

PSA：4.93000

LogP：6.08120

9-(4-(tert-butyl)phenyl)-9H-carbazole is a heterocyclic aromatic compound, which can be used in many organic synthesis. The structure of this compound is characterized by a phenyl group at the para position of the 9H-carbazole nucleus, which is connected to a tert-butyl group.

The synthesis of 9-(4-(tert-butyl)phenyl)-9H-carbazole involves the reaction of 9H-carbazole and 4-tert-butyl phenyl bromide in the presence of an inorganic base, such as sodium hydroxide, in an aqueous medium. The reaction produces a nitrogen-containing aromatic compound with a phenyl group and a tert-butyl group connected at the para position of the 9H-carbazole nucleus.

The physical properties of 9-(4-(tert-butyl)phenyl)-9H-carbazole include a melting point of 101°C, a boiling point of 287°C, a specific gravity of 1.1, and a solubility in water of 0.3 g/L. It is an off-white, crystalline solid with a faintly sweet odor.

The chemical properties of 9-(4-(tert-butyl)phenyl)-9H-carbazole are relatively stable and resistant to oxidation. It is moderately soluble in common organic solvents, such as ethanol, acetone, and chloroform. It is also soluble in benzene and slightly soluble in ether.

9-(4-(tert-butyl)phenyl)-9H-carbazole can be used as a reagent in various organic synthesis reactions, such as Friedel-Crafts, Williamson ether, and Mannich reactions. It can also be used as a starting material for the synthesis of other compounds, such as dyes and pharmaceuticals.

In conclusion, 9-(4-(tert-butyl)phenyl)-9H-carbazole is a versatile, nitrogen-containing aromatic compound with physical and chemical properties that make it suitable for use in a variety of organic synthesis reactions. Its synthesis involves the reaction of 9H-carbazole and 4-tert-butyl phenyl bromide in the presence of an inorganic base. It is a stable, off-white, crystalline solid with a faintly sweet odor and can be used as a reagent in various organic synthesis reactions.