2 4 Ethoxy 2 3 Difluoro Phenyl 6 Fluoro Phenol
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-(4-ethoxy-2,3-difluoro-phenyl)-6-fluoro-phenol
Chemical Formula C14H11F3O2
Molar Mass 270.23 g/mol
Appearance Solid (presumably, based on similar compounds)
Physical State At Room Temperature Solid
Solubility In Water Low (due to non - polar aromatic structure)
Solubility In Organic Solvents Likely soluble in common organic solvents like ethanol, acetone
Chemical Formula C14H10F3O2
Molecular Weight 268.225
Appearance Solid (predicted)
Boiling Point 343.3±42.0 °C at 760 mmHg (predicted)
Melting Point 85.0 - 89.0 °C
Flash Point 161.4±27.9 °C (predicted)
Density 1.349±0.06 g/cm3 (predicted)
Logp 3.84 (predicted)
Solubility Soluble in organic solvents like DMSO, methanol (estimated)
Pka 9.83±0.20 (predicted)
FAQ

What are the main uses of 2- (4-ethoxy-2,3-difluoro-phenyl) -6-fluoro-phenol?

2-%284-ethoxy-2%2C3-difluoro-phenyl%29-6-fluoro-phenol is 2- (4-ethoxy-2,3-difluorophenyl) -6-fluorophenol, which has a wide range of uses.

First, in the field of medicinal chemistry, it is a key intermediate for the synthesis of many drugs. Because of its unique chemical structure, fluorine and ethoxy groups endow compounds with special physicochemical properties and biological activities. By chemical reaction, it can be connected to the drug molecular structure, which can significantly improve the lipid solubility, stability and bioavailability of drugs. For example, in the development of some antifungal and antiviral drugs, this compound will be used as a starting material to construct complex drug molecules through a series of reactions to achieve specific therapeutic effects.

Second, in the field of materials science, it plays a key role in the synthesis of organic optoelectronic materials. Because it contains fluorine atoms, it can improve the electron transport performance and stability of materials. Using this compound to prepare organic Light Emitting Diode (OLED) materials can improve the luminous efficiency and service life of OLED devices; for solar cell material synthesis, it can optimize the photoelectric conversion efficiency of batteries and promote the development of new energy materials.

Third, in agricultural chemistry, it can be used as an important part of the synthesis of new pesticides. With the biological activity of its special structure, high-efficiency, low-toxicity and environmentally friendly pesticides can be developed. Pesticides based on 2- (4-ethoxy-2,3-difluorophenyl) -6-fluorophenol, which target specific crop pests or pathogens, can precisely act on target organisms, reduce the impact on non-target organisms, and achieve sustainable agricultural development.

What are the synthesis methods of 2- (4-ethoxy-2,3-difluoro-phenyl) -6-fluoro-phenol?

To prepare 2- (4-ethoxy-2,3-difluorophenyl) -6-fluorophenol, the following method can be used.

First take appropriate starting materials, such as benzene derivatives containing ethoxy and difluoro substitution, and start with fluorine-containing phenol derivatives. The two can be connected by a nucleophilic substitution reaction. In the reaction system, add a suitable base to promote the reaction. The base can be selected from potassium carbonate, sodium carbonate, etc., which can enhance the nucleophilicity of the reactants and promote the reaction process.

The reaction solvent is also very important, and polar aprotic solvents can be selected, such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), etc. Such solvents have good solubility to the reactants, can stabilize the reaction intermediates, and improve the reaction efficiency.

It is also crucial to control the reaction temperature and time. Usually, the reaction is initiated at a low temperature, so that the reactants are fully mixed and interacted, and then gradually heated to a suitable temperature to make the reaction complete. The reaction time depends on the concentration of the reactants, the reactivity and other factors, and generally takes several hours to tens of hours.

After the reaction is completed, the separation and purification of the product is indispensable. The method of extraction can be used first, and the reaction solution can be extracted with an organic solvent such as ethyl acetate and dichloromethane, and the product can be transferred to the organic phase. After column chromatography, suitable stationary and mobile phases are selected to further purify the product to obtain high-purity 2- (4-ethoxy-2,3-difluorophenyl) -6-fluorophenol.

During the operation, safety should be paid attention to, avoid contact with harmful reagents, and ensure that the reaction environment is clean to prevent impurities from affecting the reaction and product quality. In this way, the target product can be prepared.

What are the physical properties of 2- (4-ethoxy-2,3-difluoro-phenyl) -6-fluoro-phenol?

2-%284-ethoxy-2%2C3-difluoro-phenyl%29-6-fluoro-phenol, this is an organic compound, which can be called 2- (4-ethoxy-2,3-difluorophenyl) -6-fluorophenol in Chinese. Its physical properties are quite important, and it is related to the performance and application of this compound in various scenarios.

First, the appearance of this compound is usually white to off-white solid. This appearance characteristic makes it easy to distinguish and observe it in actual operation. Looking at its texture, it is often a delicate powder, and the touch may be fine and smooth.

Besides the melting point, the melting point of this substance is within a specific range. The determination of the melting point is crucial to determine the purity of the compound and the state change under different temperature conditions. By accurately measuring the melting point, it is possible to determine whether the compound is pure. If it contains impurities, the melting point often changes.

Solubility is also one of the key physical properties. This compound has a certain solubility in organic solvents such as ethanol and dichloromethane. This property makes it possible to choose a suitable solvent according to its solubility during chemical synthesis, separation and purification. When dissolved in ethanol, it may form a uniform solution, which is conducive to subsequent chemical reactions. In water, its solubility is poor. This limits its application in aqueous systems, but in the field of organic synthesis, the solubility of organic solvents provides the possibility for it to participate in many reactions.

In addition, its density also has a certain value. The physical property of density is of great significance when it comes to the measurement and mixing of substances. Knowing its density can precisely control the dosage of compounds to ensure the accuracy of experiments or production processes.

In summary, the physical properties of 2- (4-ethoxy-2,3-difluorophenyl) -6-fluorophenol, from appearance, melting point, solubility to density, play a decisive role in its application in chemical research, industrial production and many other fields. In practical applications, these physical properties need to be fully considered in order to achieve the effective utilization of this compound.

What are the chemical properties of 2- (4-ethoxy-2,3-difluoro-phenyl) -6-fluoro-phenol

2-%284-ethoxy-2%2C3-difluoro-phenyl%29-6-fluoro-phenol, the Chinese name or 2- (4-ethoxy-2,3-difluorophenyl) -6-fluorophenol. This substance has unique chemical properties and is not described in "Tiangong Kaiwu". Today, in ancient Chinese, it is said to show its properties.

This compound has phenolic hydroxyl group and is weakly acidic. The hydrogen of the phenolic hydroxyl group can be dissociated, and when it encounters a strong base, it can form a salt. In case of sodium hydroxide, phenolic hydroxyl hydrogen combines with hydroxide to form water, and the rest forms a sodium salt, which is a common acidity and alkalinity of phenols.

It contains fluorine atoms and ethoxy groups, which affect molecular polarity and spatial structure. Fluorine atoms have strong electronegativity, which changes the density of electron clouds at ortho sites, resulting in different chemical activities. The ethoxy group is the power supply group, which can increase the electron cloud density of the benzene ring and change the activity of the electrophilic substitution reaction of the benzene ring. In the electrophilic substitution, the ortho and para-sites of the ethoxy group are more easily attacked, such as halogenation and nitrification reactions, and the substituents can be introduced at the corresponding positions.

Furthermore, the structure contains two benzene rings, which have a certain conjugate system, which affects the physical and chemical properties of the compound. The conjugate system increases the stability of the molecule, and the spectral properties are also different. There may be characteristic absorption peaks in the ultraviolet spectrum, which can be used for identification.

And because of the heteroatoms such as fluorine and oxygen, hydrogen bonds can be formed. Intermolecular hydrogen bonds affect the melting boiling point and solubility. Such as in polar solvents, or due to hydrogen bonding and good solubility; and intermolecular hydrogen bonding can also increase the melting boiling point, because the destruction of hydrogen bonds requires energy. The chemical properties of this compound are determined by its functional groups and molecular structure, and may have potential applications in the fields of organic synthesis and medicinal chemistry.

What is the price of 2- (4-ethoxy-2,3-difluoro-phenyl) -6-fluoro-phenol in the market?

There is a question today, what is the market price of 2- (4-ethoxy-2,3-difluoro-phenyl) -6-fluoro-phenol. This is a specific organic compound in the field of fine chemicals, and its price is determined by many factors, just like the time of day, the location, and the change of people.

First, the cost of raw materials. The starting materials required to synthesize this compound, such as fluorine-containing and ethoxy-containing raw materials, are difficult to obtain and price fluctuations, all of which affect the whole body. If the raw materials are scarce or difficult to prepare, the price will be high; conversely, if the sources are extensive, the price may be close to the people. < Br >
Second, the simplicity of the preparation process. Complex synthesis routes require multi-step reactions and special reaction conditions, such as high temperature, high pressure, and the use of expensive catalysts, which all increase production costs and cause their prices to rise. If there is a simple and efficient process, the cost can be reduced, and the price may also be lowered.

Third, the state of market supply and demand. If the demand for this compound in the pharmaceutical, materials and other industries increases sharply, but the supply is limited, merchants will raise prices in pursuit of profit; if the market is saturated and the supply exceeds the demand, the price will automatically decline under pressure.

Fourth, the difference between quality grades. Those with high purity and few impurities are suitable for high-end fields, such as pharmaceutical research and development, and the price must be high; those with general purity are used in general industry, and the price is slightly lower.

After checking the past market conditions, there is no clear pricing of this compound. Because the price of chemical products changes rapidly, and the prices are different for different merchants, different batches, and different trading seasons. If you want to know the exact price, you must consult chemical product suppliers, distributors, or professional chemical product trading platforms and market survey reports to get accurate prices.