5-CHLORO-1-(4-FLUORO-PHENYL)-3-PIPERIDIN-4-YL-1H-INDOLE - Names and Identifiers
5-CHLORO-1-(4-FLUORO-PHENYL)-3-PIPERIDIN-4-YL-1H-INDOLE - Physico-chemical Properties
Molecular Formula | C19H18ClFN2
|
Molar Mass | 328.82 |
Density | 1.30 |
Boling Point | 473℃ |
Flash Point | 240℃ |
Storage Condition | 2-8°C(protect from light) |
5-CHLORO-1-(4-FLUORO-PHENYL)-3-PIPERIDIN-4-YL-1H-INDOLE - Upstream Downstream Industry
5-CHLORO-1-(4-FLUORO-PHENYL)-3-PIPERIDIN-4-YL-1H-INDOLE - Introduction
5-chroo-1-(4-FLUORO-PHENYL)-is an organic compound with the chemical formula C21H16ClFN2, which has an indole structure and substituents of benzene ring and piperidine ring. The following is its nature, use, preparation and safety information:
Nature:
-Appearance: Colorless or yellowish solid
-Solubility: Soluble in organic solvents such as chloroform, dichloromethane
-Melting point: About 80-85 ℃
-Molecular weight: 368.82g/mol
Use:
-Drug research: 5-CHLORO-1-(4-FLUORO-PHENYL)-is an important organic synthesis intermediate, commonly used in the synthesis of new drugs, compound exploration and drug research.
Method:
5-choro-1-(4-FLUORO-PHENYL)-is prepared in a variety of ways, and the following is a brief introduction to a common method:
1. 4-piperidinyl benzoic acid was synthesized by reacting 4-fluorobenzoic acid with 4-piperidinyl amine.
2. Use anhydrous acetic acid to rearrange 4-piperidinyl benzoic acid to generate N-benzoyl -4-piperidinamine.
3. Reacting n-benzoyl-4-piperidinamine with indole to give 5-benzoyl-3-(4-piperidinyl)-1H-indole.
4. Finally, the product reacts with chlorine to obtain the target product 5-CHLORO-1-(4-FLUORO-PHENYL)-phenyl.
Safety Information:
-The safety data of this compound is limited, so it must be handled with caution.
-Wear protective glasses and gloves during operation.
-Avoid inhalation or contact with skin to avoid harm to health.
-Avoid direct sunlight during storage, keep it sealed, and keep it away from fire and heat sources.
Last Update:2024-04-09 21:00:56