ethenediylbis[4-
(E)-1,2-Bis[4-(trifluoromethyl)phenyl]ethene
CAS: 42134-74-7
Molecular Formula: C16H10F6
ethenediylbis[4- - Names and Identifiers
| Name | (E)-1,2-Bis[4-(trifluoromethyl)phenyl]ethene |
| Synonyms | (1E) Benzene, 1, ethenediylbis[4- (E)-1,2-Bis[4-(trifluoromethyl)phenyl]ethene Benzene, 1,1'-(1E)-1,2-ethenediylbis[4-(trifluoromethyl)- |
| CAS | 42134-74-7 |
ethenediylbis[4- - Physico-chemical Properties
| Molecular Formula | C16H10F6 |
| Molar Mass | 316.25 |
| Density | 1.319±0.06 g/cm3(Predicted) |
| Melting Point | 134-135 °C(Solv: hexane (110-54-3)) |
| Boling Point | 299.7±35.0 °C(Predicted) |
ethenediylbis[4- - Introduction
(E)-1,2-bis [4-(trifluoromethyl)phenyl]ethene is an organic compound with the chemical formula C18H12F6. It is a colorless to pale yellow crystalline solid.
(E)-1,2-bis [4-(trifluoromethyl)phenyl]ethene has high thermal stability and chemical stability, and is insoluble in water at room temperature. It is soluble in organic solvents such as diethyl ether, dimethylformamide and chloroform. This compound can resist oxidation, acid and alkali attack.
This compound is commonly used as a starting material in organic synthesis reactions and can be used to synthesize complex molecular structures containing benzene rings and trifluoromethyl groups. Because of its specific electronic structure and reactivity, it has a wide range of applications in organic synthesis. It also has some applications in areas such as medicine and materials science.
Regarding the preparation method, (E)-1,2-bis [4-(trifluoromethyl)phenyl]ethene can be obtained by reacting benzyl alcohol with trifluoromethanesulfonic acid. Specific synthetic steps need to be designed for specific experimental conditions.
Regarding safety information, since (E)-1,2-BIS [4-(trifluoromethyl)phenyl]ethene is an organic compound, it is necessary to pay attention to its toxicity and danger. Safety procedures should be followed during use to avoid contact with skin and eyes. At the same time, but also stored in a sealed container, away from the fire and oxidant. In the event of an accident, appropriate emergency measures should be taken immediately and the doctor should be asked to provide relevant treatment advice.
(E)-1,2-bis [4-(trifluoromethyl)phenyl]ethene has high thermal stability and chemical stability, and is insoluble in water at room temperature. It is soluble in organic solvents such as diethyl ether, dimethylformamide and chloroform. This compound can resist oxidation, acid and alkali attack.
This compound is commonly used as a starting material in organic synthesis reactions and can be used to synthesize complex molecular structures containing benzene rings and trifluoromethyl groups. Because of its specific electronic structure and reactivity, it has a wide range of applications in organic synthesis. It also has some applications in areas such as medicine and materials science.
Regarding the preparation method, (E)-1,2-bis [4-(trifluoromethyl)phenyl]ethene can be obtained by reacting benzyl alcohol with trifluoromethanesulfonic acid. Specific synthetic steps need to be designed for specific experimental conditions.
Regarding safety information, since (E)-1,2-BIS [4-(trifluoromethyl)phenyl]ethene is an organic compound, it is necessary to pay attention to its toxicity and danger. Safety procedures should be followed during use to avoid contact with skin and eyes. At the same time, but also stored in a sealed container, away from the fire and oxidant. In the event of an accident, appropriate emergency measures should be taken immediately and the doctor should be asked to provide relevant treatment advice.
Last Update：2024-04-09 21:54:55
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QQ: 3007471201
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