1 Difluoro Trifluoromethoxy Methoxy 1 2 2 Trifluoroethylene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-[difluoro(trifluoromethoxy)methoxy]-1,2,2-trifluoroethylene
Chemical Formula C3F7O2
Molecular Weight 210.02 g/mol
Physical State gas at standard conditions
Boiling Point Approx. -22 °C
Vapor Pressure Relatively high at room temperature
Density Higher than air density
Solubility In Water Low solubility
Flammability Non - flammable
Chemical Stability Stable under normal conditions
Reactivity Can react with strong bases or reducing agents
Chemical Formula C3HF5O2
Molar Mass 164.03 g/mol
Appearance Colorless gas
Boiling Point Around -10 °C
Vapor Pressure Relatively high as it's a gas at ambient
Solubility Low solubility in water, likely soluble in organic solvents
Flammability May be non - flammable or low flammability due to fluorine content
Reactivity Can react with strong nucleophiles or under certain reaction conditions
Chemical Formula C3HF5O2
Molecular Weight 178.03 g/mol
Vapor Pressure Expected to be relatively high as it's likely volatile
Solubility In Water Low solubility, as fluorinated ethers tend to be hydrophobic
Stability Stable under normal conditions, but may react with strong oxidants
Chemical Formula C3F7O2
Molecular Weight 200.02 g/mol
Physical State Gas at room temperature
Boiling Point approx. -20 °C
Melting Point approx. -140 °C
Density approx. 1.4 g/cm³ (gas density varies with conditions)
Vapor Pressure High (due to low boiling point)
Flammability Non - flammable
Solubility Low solubility in water, soluble in some organic solvents
Stability Stable under normal conditions
Odor Odorless or very faint odor
Refractive Index Data specific to conditions (no standard value provided without context)
FAQ

What is the main use of 1- [difluoro (trifluoromethoxy) methoxy] -1,2,2-trifluoroethylene?

Diethyl (triethylmethoxy) methoxy-1,2,2-triethylpropene, which has not been seen in the scope of "Tiangong Kaiji", but is discussed in general chemical theory. It is often used as a key intermediate in the field of organic synthesis. Due to its rich active groups in the molecular structure, it can be reacted with a variety of chemical reactions to build complex organic structures.

For example, in the formation of carbon-carbon bonds, with its methoxy and alkynyl activities, it can be coupled with many halogenated hydrocarbons or alkenyl halides under suitable catalyst and reaction conditions to extend the carbon chain and prepare organic compounds with special structures and properties. It is widely used in pharmaceutical chemistry, materials science and other fields.

In materials science, it can be used to participate in polymerization reactions, introduce unique functional groups to the main or side chains of polymers, and improve the physical and chemical properties of materials, such as improving the thermal stability, mechanical properties or imparting special optical and electrical properties of materials. In the drug synthesis path, as a key building block, the drug activity skeleton is built through multi-step reactions, providing an important raw material basis for innovative drug research and development.

What are the physical properties of 1- [difluoro (trifluoromethoxy) methoxy] -1,2,2-trifluoroethylene

"Tiangong Kaiwu" says: Diane (trimethoxy) methoxy-1,2,2-trimethylpropane is also an organic compound. Its physical properties are unique and valuable for investigation.

Looking at its properties, at room temperature, diane (trimethoxy) methoxy-1,2,2-trimethylpropane is mostly liquid, with a clear and transparent color, just like the purity of morning dew. Its smell is specific, although not pungent, it also has a unique smell, which is unforgettable, as if it reveals its unique chemical structure subtly.

When it comes to density, it is lighter than water, so if placed in water, it often floats on the water surface, just like oil and water, distinct. This property allows it to be used in many chemical operations. It can be separated and purified by the difference in density.

Furthermore, its boiling point is also one of the key physical properties. Moderate heating, to a specific temperature, diane (trimethoxy) methoxy-1,2,2-trialkylpropane will boil and vaporize. This temperature point provides accurate parameters for related industrial production and experimental operations. Knowing its boiling point can precisely control the temperature in distillation, fractionation and other processes to obtain pure products.

Solubility is also a property that cannot be ignored. In organic solvents, such as ethanol and ether, diane (trimethoxy) methoxy-1,2,2-trimethylpropane exhibits good solubility and can be miscible with it to form a uniform and stable mixed system. However, in water, the solubility is poor, which also affects its application in different fields.

In summary, the physical properties of diane (trimethoxy) methoxy-1,2,2-trimethylpropane, such as properties, density, boiling point, solubility, etc., are the cornerstones of its application in chemical industry, scientific research and other fields, helping our generation to better understand and use this compound.

What are the chemical properties of 1- [difluoro (trifluoromethoxy) methoxy] -1,2,2-trifluoroethylene?

Dichloro (trichloromethyl) methoxy methane, also known as 1,2,2-trichloroethyl chloroformate, is an organic compound. Its chemical properties are quite active and have strong reactivity.

First, its hydrolysis is significant. When exposed to water, it is prone to hydrolysis to generate corresponding acids and alcohols. This hydrolysis process may be affected by the pH of the environment. In an alkaline environment, the hydrolysis rate is often accelerated, because hydroxide ions can promote the reaction.

Second, it has the ability to esterify. Esterification can occur with alcohols to form new ester compounds. This reaction usually requires the presence of a specific catalyst, and under the conditions of suitable temperature and reaction time, it can be successfully achieved.

Furthermore, in view of its chlorine atoms, in some reactions, chlorine atoms can be replaced by nucleophiles to generate different replacement products. This property makes it quite valuable in the field of organic synthesis, and can be used as an intermediate to participate in the synthesis of many complex organic compounds.

However, special attention should be paid to the fact that 1,2,2-trichloroethyl chloroformate is toxic and corrosive. When operating, strict protective measures must be taken to avoid damage to the human body. At the same time, because of its chemical activity, storage and transportation also need to follow specific specifications to ensure safety.

What is the preparation method of 1- [difluoro (trifluoromethoxy) methoxy] -1,2,2-trifluoroethylene?

The method for making diethyl ether (triethyl ether methoxy) methoxy-1,2,2-triethylunitary alkyne is as follows:

First take an appropriate amount of alcohol, such as ethanol, in the reactor. Prepare concentrated sulfuric acid and slowly add it to the alcohol. This process needs to be cautious. Because it is highly corrosive and generates heat during mixing, it must be constantly stirred to dissipate heat and prevent local overheating. The ratio of sulfuric acid to alcohol needs to be precisely controlled, usually according to specific reaction requirements.

Heat the mixture and maintain the appropriate temperature, usually between 140 and 170 degrees Celsius. The temperature is very critical. If it is too low, the reaction rate will be slow; if it is too high, it will easily cause side reactions and form impurities such as ethylene. During the reaction, pay close attention to the temperature and reaction phenomena.

After the reaction is completed, the product contains diethyl ether (triethyl ether methoxy) methoxy-1,2,2-triethylunitary alkyne and unreacted raw materials, by-products, etc. First, it is simply distilled to separate the components with large differences in boiling points. Then use a suitable desiccant, such as anhydrous calcium chloride, to remove the residual water. Then through distillation operation, according to the subtle differences in the boiling points of each component, fine separation, to obtain a pure target product.

During the operation, strict safety procedures are followed. Because the reagents used are flammable and corrosive, protective measures are taken to ensure the safety of the experiment.

1- [Difluoro (trifluoromethoxy) methoxy] -1,2,2-trifluoroethylene What are the precautions during use?

2 - (trichloroacetoxy) acetoxy - 1,2,2 - trichloroethane, also known as trichloroethyl phosphate, has the following precautions during use:

First, this substance is toxic and is related to personal safety. Its toxicity can invade the human body through respiratory tract, skin contact and accidental ingestion, and damage the nervous system, liver and other organs. Therefore, strict protective measures must be taken when using it, such as wearing a gas mask to prevent harmful gases from being inhaled; wearing protective clothing to avoid skin contact with it; washing hands and body thoroughly after operation to prevent residual poisons from endangering health.

Second, it is a flammable substance and has a high safety risk. In case of open flames, hot topics are very easy to burn, and even cause explosions. Therefore, in storage and use places, open flames and smoking behavior are strictly prohibited. Electrical equipment needs to meet explosion-proof standards, and complete fire extinguishing equipment, such as dry powder fire extinguishers, carbon dioxide fire extinguishers, etc., should be equipped for emergencies.

Third, its chemical properties are lively and easy to react with many substances. Do not store or mix with strong oxidants, strong acids, strong alkalis, etc., otherwise it may cause violent reactions and lead to dangerous situations. Before mixing with other chemical substances, be sure to understand the compatibility of the two in detail. If necessary, conduct a small test to confirm that it is safe before large-scale operation.

Fourth, storage conditions are also very important. Store in a cool and well-ventilated place, away from fire and heat sources. Storage containers must be tightly sealed to prevent leakage. At the same time, regular inspections of the storage area should be carried out to check for signs of leakage. Once problems are detected, immediate countermeasures should be taken, such as evacuating personnel, sealing the scene, and promptly starting leakage treatment work.

In short, when using 2 - (trichloroacetoxy) acetoxy - 1,2,2 - trichloroethane, the above precautions should be taken very seriously and operated in strict accordance with regulations to ensure the safety of personnel and the environment.