Methanone, (4-fluorophenyl)-1H-indol-7-yl-
Methanone, (4-fluorophenyl)-1H-indol-7-yl-
CAS: 405275-40-3
Molecular Formula: C15H10FNO
Methanone, (4-fluorophenyl)-1H-indol-7-yl- - Names and Identifiers
| Name | Methanone, (4-fluorophenyl)-1H-indol-7-yl- |
| Synonyms | (4-Fluorophenyl)(1H-indol-7-yl)methanone Methanone, (4-fluorophenyl)-1H-indol-7-yl- |
| CAS | 405275-40-3 |
Methanone, (4-fluorophenyl)-1H-indol-7-yl- - Physico-chemical Properties
| Molecular Formula | C15H10FNO |
| Molar Mass | 239.24 |
| Boling Point | |
| Storage Condition | 2-8°C |
| Sensitive | IRRITANT |
| MDL | MFCD13177625 |
Methanone, (4-fluorophenyl)-1H-indol-7-yl- - Introduction
Methanone, (4-fluorophenyl)-1H-indol-7-yl-is an organic compound with the chemical formula C16H11FNO.
Nature:
Methanone, (4-fluorophenyl)-1H-indol-7-yl-is a white solid with chemical properties similar to benzophenone. It has a strong aroma.
Use:
Methanone, (4-fluorophenyl)-1H-indol-7-yl-is an important organic synthesis intermediate. It is widely used in the field of medicine to synthesize anti-cancer drugs, antiviral drugs and antidepressants.
Preparation Method:
Methanone, (4-fluorophenyl)-1H-indol-7-yl-can be synthesized by a variety of methods. A common synthetic method is to react 4-fluorobenzanilide with indole, and obtain the target product by condensation reaction.
Safety Information:
Methanone, the specific safety information of (4-fluorophenyl)-1H-indol-7-yl-needs to be evaluated according to different applications. Because it is an organic compound, it may have certain toxicity and irritation. Use should follow proper handling and storage of chemicals and avoid contact with skin and eyes.
Nature:
Methanone, (4-fluorophenyl)-1H-indol-7-yl-is a white solid with chemical properties similar to benzophenone. It has a strong aroma.
Use:
Methanone, (4-fluorophenyl)-1H-indol-7-yl-is an important organic synthesis intermediate. It is widely used in the field of medicine to synthesize anti-cancer drugs, antiviral drugs and antidepressants.
Preparation Method:
Methanone, (4-fluorophenyl)-1H-indol-7-yl-can be synthesized by a variety of methods. A common synthetic method is to react 4-fluorobenzanilide with indole, and obtain the target product by condensation reaction.
Safety Information:
Methanone, the specific safety information of (4-fluorophenyl)-1H-indol-7-yl-needs to be evaluated according to different applications. Because it is an organic compound, it may have certain toxicity and irritation. Use should follow proper handling and storage of chemicals and avoid contact with skin and eyes.
Last Update：2024-04-09 21:04:16
