Chemical Formula | C18H6F6O5 |
Molecular Weight | 438.23 |
Appearance | Typically a solid |
Physical State At Room Temperature | Solid |
Melting Point | Specific value would require experimental data |
Boiling Point | Specific value would require experimental data |
Solubility In Common Solvents | Data needed on solubility in solvents like dichloromethane, toluene etc. |
Density | Experimental value needed |
Vapor Pressure | Experimental value required |
Stability | Stable under normal conditions if stored properly |
Chemical Formula | C18H6F6O5 |
Molecular Weight | 438.23 |
Appearance | Typically a solid (description may vary based on purity and conditions) |
Physical State At Room Temperature | Solid |
Solubility In Common Solvents | Solubility characteristics would depend on the solvent; likely has some solubility in polar organic solvents |
Melting Point | Data would need to be sourced from experimental studies |
Boiling Point | Boiling point data requires experimental determination |
Density | Specific density value would need to be measured experimentally |
Vapor Pressure | Vapor pressure would be low as it's a solid at room temperature; exact value needs measurement |
Thermal Stability | Information on decomposition temperature and stability under heat would need experimental verification |
Chemical Formula | C16H5F6O5 |
Molecular Weight | 408.2 |
Appearance | Typically a solid |
Melting Point | Data needed |
Boiling Point | Data needed |
Solubility In Common Solvents | Data needed |
Density | Data needed |
Vapor Pressure | Data needed |
Stability | Data needed |
Reactivity | Reacts with nucleophiles |
Chemical Formula | C18H6F6O5 |
Molar Mass | 432.23 g/mol |
Appearance | Solid |
Physical State At Room Temp | Solid |
Melting Point | Specific value needed from literature |
Boiling Point | Specific value needed from literature |
Solubility In Water | Low (expected due to structure) |
Solubility In Organic Solvents | Soluble in some common organic solvents like dichloromethane |
Density | Specific value needed from literature |
Stability | Stable under normal conditions, may react with strong bases and reducing agents |
What are the main uses of 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] diphthalic anhydride?
4%2C4%27-%5B2%2C2%2C2-%E4%B8%89%E6%B0%9F-1-%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E4%BA%9A%E4%B9%99%E5%9F%BA%5D%E4%BA%8C%E9%82%BB%E8%8B%AF%E4%BA%8C%E7%94%B2%E9%85%B8%E9%85%90%E7%9A%84%E4%B8%BB%E8%A6%81%E7%94%A8%E9%80%94%E6%98%AF%E4%BB%80%E4%B9%88%EF%BC%9F
This is the use of a chemical compound. 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethyl] diphenyldiacetic anhydride, its use.
First, in the field of polymer materials, it is often used for polymerization or addition. Because of its special properties, fluorine-containing groups can be used to improve the weather resistance and chemical resistance of polymer materials. Taking plastic materials as an example, the addition of this material can make plastic materials in poor environments, such as high-quality, high-quality and chemical-resistant materials, still maintain good physical properties, not easy to shape and age, and delay the use of materials.
Second, in terms of chemical reactions, it may be used for the synthesis of chemical compounds. Fluorine-containing compounds often have special biological activities, which can change the lipid solubility and replacement of chemical molecules. Taking some antibacterial compounds as examples, the introduction of fragments of this compound can increase the strength of the bacterial membrane of the compound and improve the antibacterial effect.
Third, in the field of optical materials, it can be used in devices such as optical diodes (OLEDs). Because it can improve the performance of the material, improve the optical properties of the material, improve the optical efficiency of the OLED device, improve the color of the light, and improve the display effect. It plays an important role in high-end display technology.
Therefore, 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethyl] diphenyldiacetic anhydride is indispensable in many important fields due to its own special chemical properties, promoting the development of phase development.
What are the synthesis methods of 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] diphthalic anhydride?
The synthesis method of 4,4 '- [2,2,2-trichloro-1- (trichloromethyl) ethylene] diphenol diacetate is related to the technology in the field of organic synthesis. This compound has important uses in materials science, medical chemistry and many other aspects, so it is crucial to explore its efficient synthesis method.
To synthesize this compound, the following paths can be considered. First, using phenolic compounds as starting materials, halogen atoms are introduced into the phenol ring through halogenation reaction, and then nucleophilic substitution reactions occur with halogenated hydrocarbons containing specific structures to form intermediates containing key linkage structures. Subsequently, the intermediates are acetylated and modified, and acetate groups are added to obtain the final target product. This path requires precise control of the reaction conditions, such as temperature, reaction time, and the proportion of reactants. During halogenation, too high temperature can easily cause excessive halogenation, and too low temperature will cause slow reaction and low yield.
Second, with a benzene ring derivative containing an appropriate substituent as the starting material, through a multi-step reaction, the key connection structure of 2,2,2-trichloro-1- (trichloromethyl) ethylene is first constructed, and then phenolic hydroxyl is introduced, and finally acetylation is carried out. The key to this strategy lies in the sequence and selectivity of each step of the reaction, and the protective group strategy needs to be used skillfully to avoid unnecessary side reactions. For example, when introducing certain groups, phenolic hydroxyl groups need to be protected, and then de-protected at an appropriate stage to ensure that the reaction proceeds in the predetermined direction.
Third, you can also try to use transition metal catalysis to improve the reaction efficiency and selectivity. For example, through a palladium-catalyzed coupling reaction, different fragments are connected to construct a target molecular skeleton. Although this method can effectively construct complex structures, it requires harsh reaction conditions, and the choice and dosage of catalysts will also significantly affect the reaction results.
There are many methods for synthesizing 4,4 '- [2,2,2-trichloro-1 - (trichloromethyl) ethylene] diphenol diacetate, each with its own advantages and disadvantages. In practice, it is necessary to choose the optimal method according to the availability of starting materials, reaction equipment and conditions, so as to achieve the goal of high-efficiency and high-purity synthesis.
What are the physicochemical properties of 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] diphthalic anhydride?
4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] diethyl benzoate, the physical properties are as follows:
Its appearance is mostly white to light yellow crystalline powder, with certain stability, and it is difficult to decompose or deteriorate on its own under normal conditions.
The melting point is in a specific range, about [X] ° C to [X] ° C. The melting point characteristics play a key role in its phase change at a specific temperature environment. It exists stably in solid form below the melting point. When the temperature rises above the melting point, it will gradually melt into a liquid state. < Br >
In terms of solubility, it shows good solubility in common organic solvents such as toluene and dichloromethane, and can form a uniform and stable solution system with these solvents; however, the solubility in water is extremely poor, almost insoluble, which is mainly due to the hydrophobicity of its molecular structure.
Density is also one of its important physical properties, about [X] g/cm ³, which determines its sedimentation and delamination behavior when mixed with other substances or performing related process operations.
In addition, it also has a certain degree of thermal stability, and within a specific temperature range, it will not undergo significant chemical structure changes or decomposition due to moderate fluctuations in temperature, which allows it to maintain relatively stable chemical properties in some industrial production processes involving heating or high temperature treatment.
What is the price range of 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] diphthalic anhydride in the market?
I don't know what you mean by "4%2C4%27-%5B2%2C2%2C2-%E4%B8%89%E6%B0%9F-1-%28%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%29%E4%BA%9A%E4%B9%99%E5%9F%BA%5D%E4%BA%8C%E9%82%BB%E8%8B%AF%E4%BA%8C%E7%94%B2%E9%85%B8%E9%85%90", is this a very obscure chemical name? Market prices often change from time to time and vary from situation to situation, and I have never heard of the price of this rare thing circulating in the market.
However, if you want to know its price, you should follow various channels. Or ask the experts who are good at chemistry, they may know the difficulty of preparing this thing, the cost of materials, so as to estimate its approximate price; or visit the trade name specializing in chemical reagents, where this thing may be sold, you can directly inquire about its price.
Or in various academic exchange places and professional forums, post to ask, gather everyone's wisdom, or get its price range. It is a pity that I cannot confirm the geometry of its price today. I hope you can follow these paths, or you can solve your confusion.
What are the manufacturers of 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] diphthalic anhydride?
There are many manufacturers of 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] dimethyl benzoate, which are scattered all over the world.
Toyo Caoda Co., Ltd., which is a leader in the industry. With its exquisite skills and profound heritage, its products are of high quality and have been praised in the global market. He has been working in the chemical industry for many years, has meticulous control over the production process, and strictly adheres to the quality. The 4,4' - [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] dimethyl benzoate produced is often trusted and selected by all parties.
A domestic chemical company in Jiangsu is also listed here. It constantly researches new technologies, actively introduces advanced equipment, and strives to improve the quality of its products. With its local advantages, it can respond to market needs in a timely manner and supply this product to many customers, gaining a place in the domestic market.
Another American chemical giant, driven by innovation and research and development, produces 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] dimethyl benzoate, which is unique in performance and is widely used in high-end fields. Its R & D team continues to explore and is committed to optimizing product characteristics to meet the stringent requirements of different customers.
In Europe, there are also chemical companies involved in the production of this product. They adhere to a rigorous attitude and follow high standards of production practices. The products are not only supplied in Europe, but also exported to all parts of the world.
All of these companies are important manufacturers of 4,4 '- [2,2,2-trifluoro-1- (trifluoromethyl) ethylene] dimethyl benzoate, each of which uses its own capabilities to promote the circulation and application of this product in the market.