As a leading 1,4-Bis(4-Amino-2-Trifluoromethylphenoxy)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 (4-amino-2-trifluoromethylphenoxy) benzene?
1%2C4-%E5%8F%8C%284-%E6%B0%A7%E5%9F%BA-2-%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%E8%8B%AF%E6%B0%A7%E5%9F%BA%29%E8%8B%AF%E7%9A%84%E4%B8%BB%E8%A6%81%E7%94%A8%E9%80%94%E5%9C%A8%E5%8C%BB%E8%8D%AF%E9%A1%B9%E7%9B%AE%E4%B8%AD%E6%9C%89%E5%A4%9A%E6%84%8F%E4%B9%89%E3%80%82
This compound has a specific chemical structure, and it is often a key intermediate for the synthesis of drugs with specific efficacy in the field of drug development. With the unique structure of this compound, chemists can carry out a series of chemical reactions and introduce other functional groups to obtain new drug molecules with precise pharmacological activity. For example, in the development of anti-tumor drugs, the structure of this compound can be modified to target specific molecular targets of tumor cells, block tumor cell growth and proliferation signaling pathways, and achieve the purpose of treating tumors.
It may also play an important role in the exploration of drugs for the treatment of neurological diseases. It may be possible to adjust its chemical structure, improve its affinity for neurotransmitter receptors, regulate neurotransmitter transmission, and provide new strategies for the treatment of Parkinson's disease, Alzheimer's disease and other neurological diseases.
In addition, in the field of anti-infective drug research and development, by modifying the compound, it may be endowed with antibacterial and antiviral activities. By interfering with the key metabolic processes of pathogens or inhibiting the binding of pathogens with host cells, the effect of anti-infection can be achieved.
In short, 1%2C4-%E5%8F%8C%284-%E6%B0%A7%E5%9F%BA-2-%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%E8%8B%AF%E6%B0%A7%E5%9F%BA%29%E8%8B%AF%E7%9A%84, as an important chemical raw material, provides rich space for pharmaceutical chemists to create and help develop more efficient and low-toxicity innovative drugs to meet clinical medical needs.
What are the synthesis methods of 1,4-bis (4-amino-2-trifluoromethylphenoxy) benzene?
1% 2C4-bis (4-hydroxy-2-trifluoromethylphenoxy) benzene, which is synthesized by many methods.
First, it can be prepared by the condensation reaction of p-hydroxybenzoic acid and trifluoromethylphenol. First, mix p-hydroxybenzoic acid with an appropriate condensing agent, such as dicyclohexylcarbodiimide (DCC), in a suitable organic solvent, such as dichloromethane, and stir well. Then slowly add trifluoromethylphenol, and add an appropriate amount of catalyst, such as 4-dimethylaminopyridine (DMAP), to maintain a certain temperature and reaction time. After the reaction, the pure product can be obtained through separation and purification steps, such as column chromatography.
Second, 4-halo-2-trifluoromethylphenoxy benzene is used as the starting material. The nucleophilic substitution reaction is carried out with the phenate salt. First, the phenate salt, such as sodium p-hydroxybenzoate, is dissolved in a suitable solvent, such as N, N-dimethylformamide (DMF), 4-halo-2-trifluoromethylphenoxy benzene is added, and then an appropriate amount of base is added, such as potassium carbonate. React at an appropriate temperature to fully carry out the nucleophilic substitution reaction. After the reaction is completed, the product can also be purified by extraction, recrystallization, etc. The compound can also be obtained.
Third, cross-coupling reaction catalyzed by palladium. Select suitable halogenated aromatics and phenolic compounds, and react in organic solvents such as toluene under the catalysis of palladium catalysts, such as tetra (triphenylphosphine) palladium (0), etc., in the presence of organic bases such as triethylamine. Carefully regulate the reaction temperature, time and the proportion of each reactant. After the reaction, regular separation and purification methods are used to purify the product, which is also one of the methods for synthesizing this compound.
What are the physical and chemical properties of 1,4-bis (4-amino-2-trifluoromethylphenoxy) benzene?
1%2C4-%E5%8F%8C%284-%E6%B0%A8%E5%9F%BA-2-%E4%B8%89%E6%B0%9F%E7%94%B2%E5%9F%BA%E8%8B%AF%E6%B0%A7%E5%9F%BA%29%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E5%8C%96%E5%AD%A6%E6%80%A7%E8%B4%A8%E5%A6%82%E4%B8%8B%E6%89%80%E8%BF%B0:
This compound is a special substance in the field of organic chemistry. Looking at its physical properties, under normal conditions, it may be a crystalline solid with a specific melting point and boiling point. Its melting point can be accurately determined, which is an important indicator for judging purity. Because the molecular structure contains specific functional groups, the intermolecular forces are unique, which have a great impact on the melting point and boiling point. And the substance also has characteristics of solubility in common organic solvents, and can be moderately dissolved in some organic solvents, such as ethanol, acetone, etc. This solubility is of great significance for its application in organic synthesis and separation and purification.
When it comes to chemical properties, the hydroxyl, trimethylphenyl, phenoxy and other functional groups contained in this compound endow it with rich chemical reactivity. The hydroxyl group can participate in the esterification reaction, and under the action of the catalyst with the organic acid, the corresponding ester compound is formed. This reaction is commonly used in the synthesis of organic esters. The trimethylbenzene gene has a certain electronic effect, or affects the reactivity of the peripheral functional groups, so that the compound exhibits special reactivity and selectivity in the electrophilic substitution reaction. In addition, the phenoxy group can also participate in some nucleophilic substitution reactions, and interact with suitable nucleophilic reagents to achieve molecular structure modification and transformation.
This compound may have potential application value in the fields of materials science, medicinal chemistry and other fields due to its unique physical and chemical properties. In materials science, functional materials with special properties can be prepared by means of their structural characteristics; in the field of medicinal chemistry, they can be rationally modified or developed into drug lead compounds with specific biological activities.
What is the price range for 1,4-bis (4-amino-2-trifluoromethylphenoxy) benzene in the market?
I have not heard of the price of "1% 2C4-bis (4-hydroxy-2-trifluoromethylphenoxy) benzene" in the market. This is a product of fine chemicals, and its price is determined by many factors.
First, the price of raw materials. If the raw materials required to prepare this product are scarce or difficult to produce, the price will be high, resulting in a high price of the finished product. If the supply of raw materials is sufficient and easy to obtain, the price may be slightly lower.
Second, the art of production. Advanced and efficient production processes can reduce production costs. However, if the technology is complex, energy consumption is high, and high-end equipment and professional manpower are required, the cost will increase, and the price will follow.
Third, market supply and demand. If the market demand for this product is strong and the supply is limited, the price will rise; if the supply exceeds the demand, the merchant may reduce the price and promote it.
Fourth, quality specifications. Different quality and specification requirements, production difficulty and cost are different, and the price is also different. High quality and high purity, the price is often higher.
Because I don't know the exact situation of the above factors, it is difficult to know the price range. For details, you can consult chemical product suppliers, traders, or refer to relevant chemical market reports and trading platform prices to get a more accurate price range.
What are the manufacturers of 1,4-bis (4-amino-2-trifluoromethylphenoxy) benzene?
1% 2C4-bis (4-hydroxy-2-trifluoromethylphenoxy) benzene, this compound has important applications in many fields today, and its manufacturers are also well-known.
Overseas, such as DuPont (DuPont) in the United States, has a long-standing reputation, known for its excellent chemical research and development and capacity, and has deep attainments in the field of fluorine-containing compounds. For the production of 1% 2C4-bis (4-hydroxy-2-trifluoromethylphenoxy) benzene, it has advanced technology and strict quality control system, and the products are of high quality and are widely supplied to the global high-end market.
Furthermore, Germany's BASF (BASF), as a giant in the chemical industry, has strong technical strength and rich experience in the production of fine chemicals. For this compound, BASF relies on its deep R & D accumulation and large-scale production advantages, and its products are quite competitive in the international market, meeting the needs of many industries for high-quality raw materials.
In China, Zhejiang Juhua Group also plays a pivotal role. Juhua has been deeply involved in the field of fluorine chemical industry for many years and has a complete industrial chain. For the production of 1% 2C4-bis (4-hydroxy-2-trifluoromethylphenoxy) benzene, relying on its own resources and technical advantages, the products not only occupy a certain share in the domestic market, but also gradually expand overseas business, showing a strong development trend.
Another Jiangsu Yake Technology is actively enterprising in the fields of electronic chemicals. Its production of 1% 2C4-bis (4-hydroxy-2-trifluoromethylphenoxy) benzene meets the development needs of the electronics industry. With product quality and innovation capabilities, it has emerged in the industry and provided high-quality raw material support for related industries.