Chemical Formula | C8H4F4O |
Molecular Weight | 192.11 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 175 - 177 °C |
Density | 1.38 g/cm³ |
Solubility | Soluble in organic solvents |
Flash Point | 65 °C |
Refractive Index | 1.438 |
Chemical Formula | C8H4F4O |
Molecular Weight | 192.11 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 172 - 174 °C |
Melting Point | N/A |
Density | 1.378 g/cm³ |
Solubility | Soluble in organic solvents |
Flash Point | 60 °C |
Vapor Pressure | N/A |
Refractive Index | 1.441 |
Chemical Formula | C8H4F4O |
Molar Mass | 192.11 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 167 - 169 °C |
Melting Point | N/A |
Density | 1.374 g/cm³ |
Solubility In Water | Reacts with water |
Solubility In Organic Solvents | Soluble in common organic solvents |
Vapor Pressure | N/A |
Flash Point | 59.4 °C |
Pungency | Pungent odor |
Chemical Formula | C8H4F4O |
Molecular Weight | 192.11 |
Appearance | Colorless to light yellow liquid |
Boiling Point | Around 182 - 184 °C |
Density | Approx. 1.40 g/cm³ |
Vapor Pressure | Low at room temperature |
Solubility | Soluble in organic solvents like dichloromethane, insoluble in water |
Flash Point | Relatively high, above 65 °C |
Refractive Index | Typically around 1.43 - 1.45 |
What are the main uses of 3- (trifluoromethyl) benzoyl fluoride?
Tris (trimethylphenyl) silyl ethyl ether, which is a useful compound in the field of organic synthesis. Its main uses are widely described as follows:
First, in organic synthesis reactions, it often acts as a hydroxyl protecting group. Hydroxyl groups are highly active in many chemical reactions and are prone to unnecessary side reactions. Tris (trimethylphenyl) silyl ethyl ether can react with hydroxyl groups to form a stable silicon ether structure, which effectively protects hydroxyl groups. After the reaction is completed, the silicon ether bond can be broken under specific conditions, and the hydroxyl group can be accurately reduced. In this way, the selectivity and efficiency of the synthesis reaction can be greatly improved, which helps chemists to construct complex organic molecular structures more accurately.
Second, it also has important applications in the field of materials science. Because of its specific chemical structure and physical properties, it can be used to prepare materials with special properties. For example, introducing it into polymer systems can change the solubility, thermal stability and surface properties of materials, and then lay the foundation for the development of new high-performance materials.
Third, in pharmaceutical chemistry research, tris (trimethylphenyl) silyl ethyl ether can be used as a key intermediate for the synthesis of drug molecules with specific biological activities. Through structural modification and derivatization, the activity, selectivity and pharmacokinetic properties of drug molecules can be explored and optimized, providing strong support and guarantee for the development of new drugs.
In conclusion, tris (trimethylphenyl) silyl ethyl ether, with its unique chemical properties, plays an indispensable and important role in many fields such as organic synthesis, materials science, and medicinal chemistry, promoting the sustainable development and progress of various fields.
What are the physical properties of 3- (trifluoromethyl) benzoyl fluoride?
Tris (ethyl) benzyl ammonium chloride is a very important organic compound. Its physical properties are as follows:
Looking at its appearance, under room temperature and pressure, it often appears as a white crystalline powder with a fine texture, which is visually visible to the naked eye.
As for solubility, this substance is easily soluble in water and can be quickly dispersed and dissolved in water to form a uniform solution. This property makes it convenient to participate in reactions in many chemical reactions or industrial processes involving the aqueous phase. And it can also be soluble in some polar organic solvents, such as methanol, ethanol, etc. However, in non-polar organic solvents, such as n-hexane, benzene, etc., the solubility is poor.
When it comes to melting point, tri (ethyl) benzyl ammonium chloride has a certain melting point, and this melting point temperature is a key indicator of the mutual transformation of its solid and liquid states. Its melting point is relatively high, which indicates that the substance has strong intermolecular forces and relatively stable structures. It requires a certain amount of heat from the outside world to break the intermolecular bonds and realize the transition from solid to liquid.
In addition, the substance has a certain degree of hygroscopicity. In a humid environment, it is easy to absorb moisture in the air, causing its own deliquescence. This property should be paid attention to during storage and use, and should be properly sealed to prevent moisture absorption from affecting its quality and performance. < Br >
In aqueous solution, tri (ethyl) benzyl ammonium chloride can be ionized to produce corresponding ions, showing good conductivity. This conductivity may have certain applications in some electrochemical fields or related research.
The above are the main physical properties of tri (ethyl) benzyl ammonium chloride.
What are the chemical properties of 3- (trifluoromethyl) benzoyl fluoride?
Tris (ethyl) benzyl ammonium chloride, which is a common quaternary ammonium salt compound. Its properties are as follows:
Under normal temperature, it is mostly white or slightly yellow crystalline powder, which is very soluble in water. It can ionize quaternary ammonium cations and chloride ions in water, and the solution is clear and transparent. Because of its good water solubility, it can be easily dispersed and dissolved in many aqueous systems, laying the foundation for its wide application.
When it comes to chemical properties, the chemical properties of this substance are relatively stable. However, due to the presence of quaternary ammonium cations in its molecular structure, it has a certain surface activity. This surface activity allows it to significantly reduce the surface tension in solution, thus exhibiting properties such as emulsification, dispersion, solubilization, and foaming. During the emulsification process, it can promote the formation of a relatively stable emulsion system between the immiscible oil and water phases; during the dispersion process, the solid particles can be uniformly dispersed in the liquid medium to prevent the particles from agglomerating.
Furthermore, tri (ethyl) benzyl ammonium chloride also has certain bactericidal and bacteriostatic properties. This property is derived from the ability of quaternary ammonium cations to adsorb on the surface of the cell wall of bacteria, changing the permeability of the cell wall, and then causing the material in the bacterial body to seep out, eventually causing the bacteria to die. Therefore, in many fields, such as medical and health, water treatment and food processing industries, it is often used as a fungicide and preservative to ensure environmental hygiene and product quality and safety.
In addition, in some organic synthesis reactions, it can play a role as a phase transfer catalyst. It can promote the smooth progress of the reaction between two-phase systems that are insoluble with each other (such as aqueous and organic phases), greatly improving the reaction rate and yield. This is because its cationic part can not only dissolve in the aqueous phase, but also interact with the reactants in the organic phase, so as to achieve effective transfer of the reactants between the two phases, so that the reactants that were originally difficult to contact can react smoothly.
What is the preparation method of 3- (trifluoromethyl) benzoyl fluoride?
To make tris (ethyl) benzyl ether, the method is as follows:
First take an appropriate amount of benzyl alcohol and place it in a clean reactor. For benzyl alcohol, a colorless liquid with aromatic gas is also available. The kettle is equipped with stirring, temperature control and other devices to ensure a smooth and orderly reaction.
Slowly add concentrated sulfuric acid, which is a catalyst and can promote the reaction. Sulfuric acid is strong, and caution is required when adding time to prevent it from splashing and hurting people.
Then, slowly drop in anhydrous ethanol, which is a common alcohol and a key raw material for the reaction. When dripping, control the speed to make the two fully mixed. At the same time, pay close attention to the reaction temperature. You can use a cooling device or temperature control equipment to maintain the temperature within a suitable range to prevent side reactions.
After the ethanol is added dropwise, continue to stir to make the reaction fully occur. During this reaction process, the hydroxyl group of benzyl alcohol interacts with the ethoxy group of ethanol to gradually generate tri (ethyl) benzyl ether.
After the reaction is completed, pour the reaction solution into the separation funnel and wash it with an appropriate amount of water to remove some impurities dissolved in water. Separate the organic phase and dry it with anhydrous magnesium sulfate to remove the remaining water.
Finally, the product is purified by distillation. According to the boiling point characteristics of tris (ethyl) benzyl ether, the fractions in the corresponding temperature range are collected, which is the pure tris (ethyl) benzyl ether. This process requires fine operation to obtain high-purity products.
What should be paid attention to when storing and transporting 3- (trifluoromethyl) benzoyl fluoride?
Tri (triethyl) silicoethyl ether requires attention to a number of key points when storing and transporting.
First, in terms of storage, it should be found in a cool, dry and well-ventilated place. This is because the substance may be sensitive to humidity and temperature, and high temperature or humid environment may cause it to chemically react, which in turn affects the quality. Be sure to keep away from fire and heat sources to prevent hazards such as fire or explosion. And it needs to be stored separately from oxidants, acids, alkalis, etc. Because of its active chemical properties, it is easy to react with these substances. The storage area should be equipped with suitable materials to contain leaks to prevent accidental leaks from being properly handled in a timely manner.
Second, in terms of transportation, it is necessary to ensure that the packaging is complete and sealed before transportation. Packaging materials need to be able to effectively resist external shocks and environmental influences to prevent product leakage. During transportation, it is necessary to strictly follow the relevant regulations on the transportation of hazardous chemicals and select transportation enterprises and vehicles with corresponding qualifications. Drivers and escorts should be familiar with the characteristics of the substance and emergency treatment methods. Transportation vehicles need to be equipped with fire extinguisher materials and leakage emergency treatment equipment. If there is an emergency situation on the way, they can respond quickly. It is necessary to avoid transportation vehicles staying in high temperature periods or densely populated areas for a long time to reduce latent risk. Therefore, when storing and transporting tri (triethyl) silicoethyl ether, comprehensive attention should be paid to the above points to ensure its safety and stability and avoid accidents.