1H-Indol-4-amine, N,1-diphenyl-
N,N-diphenyl-1H-indol-4-amine
CAS: 924900-76-5
Molecular Formula: C20H16N2
1H-Indol-4-amine, N,1-diphenyl- - Names and Identifiers
| Name | N,N-diphenyl-1H-indol-4-amine |
| Synonyms | N,N-diphenyl-1H-indol-4-amine N,1-Diphenyl-1H-indol-4-amine 1H-Indol-4-amine, N,1-diphenyl- |
| CAS | 924900-76-5 |
1H-Indol-4-amine, N,1-diphenyl- - Physico-chemical Properties
| Molecular Formula | C20H16N2 |
| Molar Mass | 284.35 |
| Density | 1.11±0.1 g/cm3(Predicted) |
| Boling Point | 482.2±27.0 °C(Predicted) |
| pKa | 4?+-.0.40(Predicted) |
1H-Indol-4-amine, N,1-diphenyl- - Introduction
N,N-diphenyl-1H-indol-4-amine is an organic compound with the chemical formula C20H16N2. It took the form of a white crystalline solid.
N,N-diphenyl-1H-indol-4-amine has some special properties because its structure contains indole ring and benzene ring. It has high solubility in organic solvents, but low solubility in water. Its melting point is about 138-140°C.
N,N-diphenyl-1H-indol-4-amine have a variety of uses in organic synthesis. It can be used as a fluorescent dye for labeling biological molecules and studying fluorescence properties. In addition, it can also be used in catalytic reactions in organic synthesis, heterocyclic synthesis and pharmaceutical research.
A common method for preparing N,N-diphenyl-1H-indol-4-amine is through the condensation reaction of aniline and indole. First, aniline reacts with indole under basic conditions to form the corresponding amide. Then, the amide is subjected to a reduction reaction to obtain the target product N,N-diphenyl-1H-indol-4-amine.
Regarding safety information, according to limited information, N,N-diphenyl-1H-indol-4-amine generally do not cause direct harm to the human body under normal conditions of use. However, as an organic compound, it needs to follow general laboratory safety practices, avoid contact with skin and eyes, and ensure that it is used in a well-ventilated environment. If necessary, it should be used and operated under the guidance of chemical professionals.
N,N-diphenyl-1H-indol-4-amine has some special properties because its structure contains indole ring and benzene ring. It has high solubility in organic solvents, but low solubility in water. Its melting point is about 138-140°C.
N,N-diphenyl-1H-indol-4-amine have a variety of uses in organic synthesis. It can be used as a fluorescent dye for labeling biological molecules and studying fluorescence properties. In addition, it can also be used in catalytic reactions in organic synthesis, heterocyclic synthesis and pharmaceutical research.
A common method for preparing N,N-diphenyl-1H-indol-4-amine is through the condensation reaction of aniline and indole. First, aniline reacts with indole under basic conditions to form the corresponding amide. Then, the amide is subjected to a reduction reaction to obtain the target product N,N-diphenyl-1H-indol-4-amine.
Regarding safety information, according to limited information, N,N-diphenyl-1H-indol-4-amine generally do not cause direct harm to the human body under normal conditions of use. However, as an organic compound, it needs to follow general laboratory safety practices, avoid contact with skin and eyes, and ensure that it is used in a well-ventilated environment. If necessary, it should be used and operated under the guidance of chemical professionals.
Last Update：2024-04-09 21:01:54
