2-AMino-4-(3-indolyl)pyriMidine
4-(1H-Indol-3-yl)pyrimidin-2-amine
CAS: 289628-76-8
Molecular Formula: C12H10N4
2-AMino-4-(3-indolyl)pyriMidine - Names and Identifiers
2-AMino-4-(3-indolyl)pyriMidine - Physico-chemical Properties
| Molecular Formula | C12H10N4 |
| Molar Mass | 210.23 |
| Storage Condition | Room Temprature |
| Sensitive | Irritant |
| MDL | MFCD11058049 |
2-AMino-4-(3-indolyl)pyriMidine - Introduction
4-(1H-Indol-3-yl)pyrimidin-2-amine is an organic compound with the chemical formula C12H10N4. It is a white crystalline solid, slightly soluble in water and readily soluble in solvents. The compound is stable at room temperature.
One of the main uses of this compound is in the field of pharmaceutical research, as a synthetic intermediate for drug molecules. Because of its high biological activity, it can be used as a precursor of anticancer drugs or the starting point of drug development.
The method for preparing the compound can be completed by a multi-step reaction. A common method is to use 1H-Indole as the starting material and synthesize it through a series of steps such as hydrogenation reaction, N-formylation reaction, reduction reaction, acylation reaction and aminane reaction.
There is no specific report on the safety information of this compound. However, during the experimental operation, appropriate protective measures should be taken to avoid inhalation, ingestion and contact with the skin. At the same time, in the operation should pay attention to comply with the relevant safety procedures, such as wearing protective glasses and gloves, operating in a well-ventilated laboratory environment. In case of any discomfort or accident, medical assistance should be sought immediately.
One of the main uses of this compound is in the field of pharmaceutical research, as a synthetic intermediate for drug molecules. Because of its high biological activity, it can be used as a precursor of anticancer drugs or the starting point of drug development.
The method for preparing the compound can be completed by a multi-step reaction. A common method is to use 1H-Indole as the starting material and synthesize it through a series of steps such as hydrogenation reaction, N-formylation reaction, reduction reaction, acylation reaction and aminane reaction.
There is no specific report on the safety information of this compound. However, during the experimental operation, appropriate protective measures should be taken to avoid inhalation, ingestion and contact with the skin. At the same time, in the operation should pay attention to comply with the relevant safety procedures, such as wearing protective glasses and gloves, operating in a well-ventilated laboratory environment. In case of any discomfort or accident, medical assistance should be sought immediately.
Last Update：2024-04-09 21:54:55
