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Name: 11-Phenyl-11,12-dihydroindolo[2,3-a]carbazole   

CAS NO: 1024598-06-8

Purity: 99% min

MF: C24H16N2

MW:332.397

BP:598.8±32.0 °C at 760 mmHg

Density: 1.3±0.1 g/cm3

MP: N/A

EINECS:N/A

Appearance: White Powder

Package: 25g, 100g, 500g, bulk package

Application:Organic Synthesis intermediate

Other name:

N-(2-Indanyl)aniline;

Indolo[2,3-a]carbazole, 11,12-dihydro-11-phenyl-;

N-Phenylindan-2-amine;

2-aminophenylindane;

indan-2-yl anilide;

N-phenylindolo[2,3-a]carbazole;

11,12-Dihydro-11-phenylindolo[2,3-a]carbazole;

Synthesis of 11,12-Dihydro-11-phenyl-indolo [2,3-a] carbazole CAS NO: 1024598-06-8

1 - amino - N - phenyl carbazole as starting materials, the selective bromination reaction Suzuki coupling reaction and as Buchwald coupling reaction was synthesized, 11, 12 - dihydro - 11 - phenyl - indole [2, 3 - a] carbazole CAS NO: 1024598-06-8, through the NMR to the compound structure characterization. Studied the factors such as reaction temperature, catalyst reaction time influencing on the yield of target compounds, it is concluded that the best reaction conditions: reaction temperature is 90, the reaction time of 26 h, dosage of catalyst palladium acetate for 1 - amino - N - phenyl carbazole molar volume of 4%.

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