Trifluoro Trifluoromethoxy Ethylene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
Trifluoro(trifluoromethoxy)ethylene
Chemical Formula C3F6O
Molecular Weight 166.02 g/mol
Appearance Colorless gas
Boiling Point Around -27.4 °C
Density At standard conditions, gas density is relevant, molar volume calculations can estimate its gas - phase density at STP
Solubility Low solubility in water, likely more soluble in non - polar organic solvents
Vapor Pressure Relatively high as a gas at normal temperatures
Flammability May be flammable under certain conditions
Reactivity Highly reactive due to the presence of multiple fluorine atoms and the unsaturated double bond
Chemical Formula C3F6O
Molecular Weight 166.02 g/mol
Appearance Colorless gas
Boiling Point -25.7 °C
Melting Point -143.8 °C
Density 1.54 g/cm³ (gas at 25 °C)
Vapor Pressure High (being a gas)
Solubility In Water Low (hydrophobic due to fluorine groups)
Flammability Non - flammable
Reactivity Reactive towards nucleophiles due to the presence of double bond
Chemical Formula C3F6O
Molecular Weight 186.02 g/mol
Appearance Colorless gas
Boiling Point -27 °C
Melting Point -157 °C
Density 1.51 g/cm³ (gas, at 25 °C and 1 atm)
Vapor Pressure High (due to gaseous state at room conditions)
Solubility In Water Low (hydrophobic, non - polar compound)
Odor Odorless (estimated as a fluorinated compound without strong odor - producing functional groups)
Chemical Formula C3F6O
Molar Mass 166.02 g/mol
Appearance Colorless gas
Boiling Point -27.4 °C
Flammability Flammable
Stability Stable under normal conditions
FAQ

What is the main use of trifluoro (trifluoromethoxy) ethylene?

Trifluoro (trifluoromethoxy) ethylene is also an organic compound. Its main use is related to many fields.

In the field of material science, it is often used as a raw material for the creation of special polymers. The polymer made from this compound has extraordinary properties. Its fluorine-containing structure gives excellent chemical stability, which can resist the attack of many chemical substances, and maintains the integrity of the material in harsh chemical environments. And it has excellent thermal stability. It can maintain stable performance at high temperatures and does not easily decompose or deform, which is essential for material application in high temperature operating scenarios.

In the electronics industry, it also has significant functions. Due to its special electrical properties, it can be used as an insulating material for electronic devices. It can effectively prevent current leakage, ensure stable operation of electronic equipment, and improve equipment reliability and service life. At the same time, its low dielectric constant can reduce signal transmission loss, which is of great significance in the field of high-speed electronic communication, helping to improve data transmission efficiency and quality.

In the field of medical chemistry, trifluoromethoxy ethylene may be an intermediate for the synthesis of specific drugs. Its unique chemical structure can change the biological activity and pharmacokinetic properties of compounds, helping chemists create new drugs with high selectivity, strong activity and low toxic and side effects, making great contributions to human health.

In summary, trifluoromethoxy ethylene plays a key role in materials, electronics, medicine and other fields, promoting technological innovation and development in various industries.

What are the physical properties of trifluoro (trifluoromethoxy) ethylene

Trifluoro (trifluoromethoxy) ethylene has unique physical properties. Its properties are colorless and volatile, and it is gaseous at room temperature and pressure. It is light and easy to disperse.

When it comes to boiling point, it is very low, about -20 ° C. This property allows it to quickly vaporize at lower temperatures. The melting point is also quite low, about -150 ° C, showing that it changes from solid to liquid at low temperatures.

The density is higher than that of common gases, about 4.5g/L. This density characteristic makes its distribution in a specific space different from that of common gases.

In terms of solubility, trifluoro (trifluoromethoxy) ethylene is insoluble in water, but soluble in some organic solvents, such as dichloromethane, chloroform, etc. In organic solvents, it can exhibit specific physical and chemical interactions.

Its vapor pressure also has characteristics. At room temperature, the vapor pressure is relatively high, indicating that its gasification trend is strong, and the dynamic balance between the gas phase and the liquid phase of the molecule is inclined to the gas phase side.

The dielectric constant is relatively low, which affects its electric polarization behavior in the electric field environment, and has a unique performance in electrical related applications.

The above physical properties make trifluoroethylene (trifluoromethoxy) ethylene show different uses and potential value in many fields such as chemical engineering and materials science.

What are the chemical properties of trifluoro (trifluoromethoxy) ethylene

Trifluoro (trifluoromethoxy) ethylene, which is a kind of organic fluoride. Its chemical properties are unique and have many specificities.

In terms of its stability, it is endowed with high chemical stability due to the rich fluorine atoms in its molecular structure. Fluorine atoms have high electronegativity and strong C-F bond energy, which makes the substance relatively inert to many chemical reagents. Under normal conditions, it is difficult to chemically react.

In terms of its reactivity, although the overall stability is high, it can also exhibit certain reactivity under specific conditions. For example, under extreme conditions such as strong Lewis acids or high temperatures, its carbon-carbon double bond can participate in the addition reaction, just like the typical reaction of olefins. However, due to the electronic and spatial effects of surrounding fluorine atoms, this addition reaction will be different from that of ordinary olefins. The electron-absorbing effect of fluorine atoms will reduce the electron cloud density of the double bond, making the electrophilic addition reaction more difficult; however, it may be more conducive to the nucleophilic addition reaction.

Its solubility characteristics, in view of the presence of many fluorine atoms in the molecule, the substance has certain hydrophobicity. In common organic solvents, the solubility may be limited, while in some fluorine-containing organic solvents, the solubility may be better.

Volatility, due to relatively small molecules and the influence of fluorine atoms, has a certain degree of volatility. However, compared with some simple hydrocarbons, because their intermolecular forces are changed by the action of fluorine atoms, the volatility is not extremely high.

Thermal stability is also quite impressive. At higher temperatures, the molecular structure can be maintained relatively stable, and it is not easy to decompose rapidly due to heat. This property makes it an advantage in some application scenarios that require thermal stability.

In short, trifluoromethoxy ethylene has chemical properties such as high stability, reactivity under specific conditions, special solubility and volatility, and good thermal stability due to its unique molecular structure.

What is the production method of Trifluoro (trifluoromethoxy) ethylene?

Trifluoromethoxy (trifluoromethoxy) ethylene is also an organic compound. The method of its preparation has been obtained by several steps in the past.

One method starts with a halogenated hydrocarbon containing fluorine, and interacts with alkali metal alkoxides or phenolates in a suitable solvent at a mild temperature and under stirring. In this reaction, the halogen atom leaves, and the alkoxide or phenate group joins to obtain an intermediate product. For example, by reacting chlorotrifluoromethane with alkoxides, through the mechanism of nucleophilic substitution, the chlorine is replaced by an alkoxy group to form a fluorine-containing ether intermediate.

Second, the intermediate is eliminated. A strong base such as sodium alcohol is often used to remove hydrogen halide or other small molecules from the molecule under heating conditions to form a carbon-carbon double bond, and then trifluoro (trifluoromethoxy) ethylene is obtained. This process requires precise temperature control to promote elimination and avoid side reactions.

And fluoroolefins are used as raw materials to react with reagents containing trifluoromethoxy groups with the help of catalysts. For example, a transition metal catalyst is used to catalyze the addition reaction of fluoroolefins with trifluoromethoxy sources, and then after appropriate conversion, the target product can also be obtained. This catalyst needs to be selected with good activity and selectivity, and the regulation of reaction conditions is crucial, such as temperature, pressure and the proportion of reactants, all of which are related to yield and purity.

The method of preparing trifluoro (trifluoromethoxy) ethylene has its own advantages and disadvantages. It is necessary to consider the availability of raw materials, the cost, the difficulty of reaction and the purity of the product according to actual needs, and choose the appropriate method.

Trifluoro (trifluoromethoxy) ethylene in the use of what are the precautions

Trifluoro (trifluoromethoxy) ethylene is a special chemical substance, and many things must be paid attention to during use.

Those who bear the brunt must take comprehensive safety precautions. This substance has certain chemical activity and potential danger, and operators should strictly follow safety procedures. Complete protective measures are indispensable. Wear protective clothing, protective gloves and goggles to prevent it from coming into contact with the skin and eyes. If it is accidentally touched, rinse with plenty of water immediately and seek medical attention in time. Due to its irritation and toxicity, the operating environment should be well ventilated to prevent physical discomfort caused by inhalation. If necessary, respiratory protective equipment should be equipped.

Furthermore, storage conditions should not be underestimated. It should be stored in a cool, dry and ventilated place, away from fire and heat sources, and protected from direct sunlight. Separate from oxidants, acids, bases and other substances, and must not be mixed and stored to avoid dangerous chemical reactions.

During use, precise control of dosage and reaction conditions is essential. Due to its unique reactivity, factors such as dosage, reaction temperature, pressure and time have a profound impact on the reaction results. Therefore, it is necessary to rely on precise experimental design and operation to strictly control each parameter to ensure that the reaction proceeds in the expected direction and avoid the occurrence of unexpected side reactions.

In addition, in-depth understanding of its chemical properties is also key. Familiar with its reaction characteristics under different conditions, in order to cope with the use of freely, in advance to prepare risk anticipation and response strategies.

In short, the use of trifluoromethoxy ethylene, need to be scientific and rigorous attitude, comprehensive consideration of safety, storage, operation and many other links, to ensure the smooth and orderly process, to avoid accidents.