383861-22-1
5-(4-piperidyl)-1H-indole
CAS: 383861-22-1
Molecular Formula: C13H16N2
383861-22-1 - Names and Identifiers
| Name | 5-(4-piperidyl)-1H-indole |
| Synonyms | 4-(5'-Indole)piperidine 5-(4-piperidyl)-1H-indole 5-Piperidin-4-yl-1H-indole 1H-Indole, 5-(4-piperidinyl)- |
| CAS | 383861-22-1 |
| InChI | InChI=1/C13H16N2/c1-2-13-12(5-8-15-13)9-11(1)10-3-6-14-7-4-10/h1-2,5,8-10,14-15H,3-4,6-7H2 |
383861-22-1 - Physico-chemical Properties
| Molecular Formula | C13H16N2 |
| Molar Mass | 200.28 |
| Density | 1.118g/cm3 |
| Boling Point | 388.6°C at 760 mmHg |
| Flash Point | 188.8°C |
| Vapor Presure | 3.03E-06mmHg at 25°C |
| Storage Condition | 2-8°C |
| Refractive Index | 1.622 |
383861-22-1 - Introduction
5-(4-piperidyl)-1H-indole, also known as 5-(4-piperidyl)-1H-indole, is an organic compound. Its chemical formula is C15H16N2 and its relative molecular mass is 220.30g/mol.
Regarding its properties, 5-(4-piperidyl)-1H-indole is a white to light yellow solid with an indole-like odor. It is stable at room temperature, but may decompose at high temperatures. The compound is dissolved in some organic solvents, such as ethanol, methanol and dichloromethane.
One of the main uses of this compound is as a pharmaceutical intermediate. It has important applications in the field of medicine, and can be used to synthesize biologically active molecules, such as anti-tumor drugs, anti-inflammatory drugs, etc.
A common method for preparing 5-(4-piperidyl)-1H-indole is through the reaction of indole with 4-piperidinecarboxaldehyde. The reaction is usually carried out under an inert atmosphere, such as ethanol solution under the protection of nitrogen.
Regarding safety information, due to the lack of relevant studies, there is little information on the toxicity and safety of 5-(4-piperidyl)-1H-indole. However, as an organic compound, care should be taken to use personal protective equipment to avoid skin contact and inhalation. At the same time, the compound should be stored and handled properly to avoid contact with oxygen, heat and flammable materials to reduce potential hazards. In use, reference should be made to the relevant safety data sheets and experimental practices.
Regarding its properties, 5-(4-piperidyl)-1H-indole is a white to light yellow solid with an indole-like odor. It is stable at room temperature, but may decompose at high temperatures. The compound is dissolved in some organic solvents, such as ethanol, methanol and dichloromethane.
One of the main uses of this compound is as a pharmaceutical intermediate. It has important applications in the field of medicine, and can be used to synthesize biologically active molecules, such as anti-tumor drugs, anti-inflammatory drugs, etc.
A common method for preparing 5-(4-piperidyl)-1H-indole is through the reaction of indole with 4-piperidinecarboxaldehyde. The reaction is usually carried out under an inert atmosphere, such as ethanol solution under the protection of nitrogen.
Regarding safety information, due to the lack of relevant studies, there is little information on the toxicity and safety of 5-(4-piperidyl)-1H-indole. However, as an organic compound, care should be taken to use personal protective equipment to avoid skin contact and inhalation. At the same time, the compound should be stored and handled properly to avoid contact with oxygen, heat and flammable materials to reduce potential hazards. In use, reference should be made to the relevant safety data sheets and experimental practices.
Last Update：2024-04-09 21:54:55
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