As a leading 1,4-Bis[1-[(4-Ethenylphenyl)Methoxy]-2,2,2-Trifluoro-1-(Trifluoromethyl)Ethyl] Benzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the main uses of 1,4-Bis [1- [ (4-Ethenylphenyl) Methoxy] -2,2,2-Trifluoro-1- (Trifluoromethyl) Ethyl] Benzene?
1% 2C4 - Bis% 5B1 -% 5B% 284 - Ethenylphenyl%29Methoxy%5D - 2% 2C2% 2C2 - Trifluoro - 1 - %28Trifluoromethyl%29Ethyl%5D + Benzene is an organic compound with a long and complex name and contains a lot of chemical group information. This compound may have important uses in the chemical industry, materials science and other fields.
In the chemical industry, or as a key intermediate. It can be combined with other compounds through specific chemical reactions to participate in the construction of more complex organic molecules. This process is similar to the ancient skilled craftsmen who built exquisite castles with basic components. Each step needs to be precisely controlled to create the desired product. With its unique chemical structure, it can endow the final product with specific properties, such as improved solubility and stability, etc., as if it is a strong and practical "coat" for the product.
In the field of materials science, or as a raw material for the preparation of new functional materials. With the development of science and technology, the requirements for material properties are increasingly stringent. The special groups contained in this compound may endow the material with excellent optical and electrical properties, or excellent chemical resistance. For example, in the preparation of high-performance optical materials, their structural properties may give the material unique light refraction and absorption characteristics, which is like injecting a unique "visual ability" into the material, making it stand out in the field of optical devices; in the preparation of corrosion-resistant materials, it can rely on its fluorine-containing group properties to enhance the material's resistance to chemical attack, just like casting an indestructible "armor" for the material.
In short, 1% 2C4 - Bis% 5B1 -% 5B% 284 - Ethenylphenyl%29Methoxy%5D - 2% 2C2% 2C2 - Trifluoro - 1 - %28Trifluoromethyl%29Ethyl%5D + Benzene, although the name is obscure, is like a key role hidden behind the scenes in the field of chemical and materials science involved in the development of modern science and technology, silently promoting the birth of many innovative achievements.
What are the physical properties of 1,4-Bis [1- [ (4-Ethenylphenyl) Methoxy] -2,2,2-Trifluoro-1- (Trifluoromethyl) Ethyl] Benzene?
1% 2C4 - Bis% 5B1 -% 5B% 284 - Ethenylphenyl%29Methoxy%5D - 2% 2C2% 2C2 - Trifluoro - 1 - %28Trifluoromethyl%29Ethyl%5D + Benzene, this is an organic compound, its physical properties are as follows:
In terms of view, it is either a solid state or a liquid state, but the exact state depends on the ambient temperature and pressure. The melting point of this compound is related to the strength of the intermolecular force. The stronger the intermolecular force, the higher the melting point. It contains many fluorine atoms. Due to the extremely high electronegativity of fluorine atoms, or the formation of strong intermolecular forces, the melting point is increased.
In terms of boiling point, the compound needs to overcome the intermolecular force if it wants to boil. In view of the fact that its molecular structure contains many fluorine atoms, and the structure is relatively complex, the intermolecular force is quite large, so the boiling point may be higher.
In terms of solubility, because the molecule contains both fluorine-containing hydrophobic parts and benzene-containing ring structural parts. According to the principle of similar phase solubility, it may have certain solubility in polar organic solvents such as acetone and acetonitrile, but in water, due to the large number of hydrophobic groups, the solubility may be poor.
Density is also an important physical property. The fluorine atoms in the molecule have a large relative mass, and the compound has a certain compactness, so that its density may be greater than that of common organic solvents or similar to that of some halogenated hydrocarbons.
In addition, the refractive index of the compound is also closely related to the molecular structure. The structures of benzene ring, carbon-carbon double bond and many fluorine atoms in the molecule will affect the speed and direction of light propagation, and then affect the refractive index. Due to the specific numerical fertilization to determine the molecular structure and measurement conditions, the exact refractive index needs to be determined accurately by experiments.
What are the chemical properties of 1,4-Bis [1- [ (4-Ethenylphenyl) Methoxy] -2,2,2-Trifluoro-1- (Trifluoromethyl) Ethyl] Benzene?
1% 2C4 - Bis% 5B1 -% 5B% 284 - Ethenylphenyl%29Methoxy%5D - 2% 2C2% 2C2 - Trifluoro - 1 - %28Trifluoromethyl%29Ethyl%5D + Benzene, this is an organic compound, which is composed of complex atomic combinations to construct its structure. Looking at its structure, the benzene ring is based, and specific groups are connected on both sides. It contains fluorine atoms, vinyl phenyl groups and methoxy groups. This unique structure endows it with diverse chemical properties.
In terms of stability, due to the presence of multiple fluorine atoms, fluorine atoms have strong electronegativity and high C-F bond energy, which can enhance molecular stability. It is more difficult to react in many environments, and has good chemical resistance and thermal stability.
In terms of solubility, because its molecule contains fluoroalkyl groups, it has certain hydrophobicity, and its solubility in polar solvents is not good; while in non-polar or weakly polar organic solvents, such as toluene and dichloromethane, it may have good solubility.
In terms of reactivity, the presence of vinyl is the key. Vinyl is unsaturated and can undergo addition reactions, such as with halogens, hydrogen halides and other electrophilic reagents. Under appropriate conditions, double bonds can be opened and added. It can also participate in polymerization reactions. Under the action of initiators, multiple vinyl groups of this molecule are connected to each other to form polymer, expanding its application range.
In addition, although the benzene ring is stable, the electron cloud density distribution of the benzene ring changes due to the influence of the substituent, which makes the electrophilic substitution reaction activity on the benzene ring different from that of benzene. Methoxy group is the power supplier group, or the electron cloud density of the adjacent and para-sites of the benzene ring increases, and the electrophilic substitution reaction is more likely to occur at these locations.
What is the production method of 1,4-Bis [1- [ (4-Ethenylphenyl) Methoxy] -2,2,2-Trifluoro-1- (Trifluoromethyl) Ethyl] Benzene?
1% 2C4 - Bis% 5B1 -% 5B% 284 - Ethenylphenyl%29Methoxy%5D - 2% 2C2% 2C2 - Trifluoro - 1 - %28Trifluoromethyl%29Ethyl%5D + Benzene, this is an organic compound. The preparation method often involves several steps of reaction, let me go through it in detail.
The choice of starting materials is related to the success or failure of the synthesis. Compounds containing benzene rings, alkenyl groups, and fluoroalkyl groups are commonly used as the starting point. One method can be as follows: First take the halogenate containing the benzene ring, make it and the alcohol containing alkenyl groups, store it in the base and phase transfer catalyst, and carry out nucleophilic substitution reaction. Bases such as potassium carbonate and phase transfer catalysts such as tetrabutylammonium bromide can promote the reaction, so that the halogen atom is replaced by alkenyl oxide to obtain an intermediate.
In the next step, reagents containing trifluoromethyl and difluoride are used to react with the above intermediates. This reaction requires a specific catalyst and reaction conditions, or a metal catalyst, such as palladium catalyst, can help it form a carbon-carbon bond or a carbon-heteroatomic bond, and trifluoromethyl and difluoroethyl are introduced into the molecule to obtain the final target product 1% 2C4 - Bis% 5B1 -% 5B% 284 - Ethenylphenyl%29Methoxy%5D - 2% 2C2% 2C2 - Trifluoro - 1 - %28Trifluoromethyl%29Ethyl%5D + Benzene.
However, the synthesis path is not limited to one end. Different starting materials and reaction conditions can cause different synthesis paths. In practice, it is necessary to consider many factors such as the availability of raw materials, the difficulty of reaction, yield and purity, and carefully design and optimize the synthesis route to achieve the purpose of efficient preparation.
What is the market outlook for 1,4-Bis [1- [ (4-Ethenylphenyl) Methoxy] -2,2,2-Trifluoro-1- (Trifluoromethyl) Ethyl] Benzene?
1% 2C4 - Bis% 5B1 -% 5B% 284 - Ethenylphenyl%29Methoxy%5D - 2% 2C2% 2C2 - Trifluoro - 1 - %28Trifluoromethyl%29Ethyl%5D + Benzene, this is an organic compound. The analysis of its market prospects should be viewed from various perspectives.
From the field of materials science, today, with the rapid development of science and technology, the demand for high-performance materials is increasing. This compound has a unique chemical structure, or it has emerged in the creation of new polymer materials. For example, due to the presence of fluorine-containing groups, it may endow materials with excellent chemical stability, low surface energy and good weather resistance. In the field of aerospace, aircraft require materials that can withstand extreme environments. This compound may be developed into an ideal material for aircraft shells and internal components, with promising prospects.
In the field of electronics, electronic devices continue to evolve towards miniaturization and high performance. The compound may be an alternative material for new electronic components due to its unique electrical properties. For example, in the field of organic semiconductor materials, its structure may endow the material with good carrier transport properties, and it is expected to be applied to the manufacture of organic Light Emitting Diodes (OLEDs), organic field effect transistors (OFETs) and other devices, with great market potential.
However, looking at its marketing activities, there are also challenges. First, the synthesis of this compound or process is complicated and expensive, resulting in high product prices, limiting its large-scale application. Second, when new compounds are put into the market, they need to undergo strict security evaluation and regulatory approval. This process is time-consuming and laborious, delaying their commercialization process.
But overall, with technological progress, the demand for materials with unique properties will increase day by day. If the synthesis cost problem can be overcome, through security evaluation, 1% 2C4 - Bis% 5B1 -% 5B% 284 - Ethenylphenyl%29Methoxy%5D - 2% 2C2% 2C2 - Trifluoro - 1 - %28Trifluoromethyl%29Ethyl%5D + Benzene will usher in broad market prospects in materials, electronics and other fields, becoming a new force to promote the development of related industries.