Chemical Formula | C6H5BF2O2 |
Molecular Weight | 155.91 |
Appearance | White to off - white solid |
Cas Number | 871332-60-8 |
Melting Point | 139 - 144 °C |
Solubility In Water | Slightly soluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, ethyl acetate |
Pka Value | Around 8 - 9 (approximate value for boronic acid group) |
Chemical Formula | C6H5BF2O2 |
Molar Mass | 155.91 g/mol |
Appearance | White to off - white solid |
Melting Point | 140 - 145 °C |
Solubility In Water | Slightly soluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
Pka | Around 8 - 9 |
Stability | Stable under normal conditions, but sensitive to moisture |
Cas Number | 219943-75-6 |
Boiling Point | Decomposes before boiling |
Chemical Formula | C6H5BF2O2 |
Molecular Weight | 157.91 |
Appearance | White to off - white solid |
Melting Point | 155 - 159 °C |
Solubility In Water | Slightly soluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
Pka | Around 8.5 - 9.5 (boronic acid group) |
Stability | Stable under normal conditions, but sensitive to strong oxidizing agents |
What are the main uses of 2,4-difluorophenylboronic acid?
2% 2C4-diethylbenzoic acid, although it has not been inked in ancient books such as Tiangong Kaiwu, it is widely used in the field of chemistry today.
First, in organic synthesis, it is often used as a key intermediate. If you want to make esters with specific structures, 2% 2C4-diethylbenzoic acid can be esterified with alcohols under acid catalysis to form corresponding esters. Such esters may have a special aroma and have a place in the fragrance industry; or in the synthesis of polymer materials, they can be used as monomers to participate in polymerization reactions, giving materials unique properties.
Second, in the field of medicinal chemistry, it is valuable. Because of its specific chemical structure, it may be modified to become a leading compound with biological activity. Medical researchers have used this as a basis to further explore its interaction with biological targets, and after multiple rounds of optimization, they may be able to develop new drugs for disease treatment.
Third, in the field of materials science, 2% 2C4-diethylbenzoic acid can be introduced into the material matrix after appropriate treatment to change the surface properties and crystallization behavior of the material. For example, adding it to some polymer materials can improve the thermal stability and mechanical properties of the material and broaden the application scenarios of the material.
In summary, although 2% 2C4-diethylbenzoic acid is not commonly found in traditional ancient books, it plays an important role in many aspects such as organic synthesis, pharmaceutical research and development, and material modification in the current chemical-related industries, promoting technological innovation and development in various fields.
What are the physical properties of 2,4-difluorophenylboronic acid?
2% 2C4-diethyladipic acid, this substance is an organic compound. Its physical properties are quite unique.
Looking at its appearance, it is often in the state of white crystalline powder, like fine salt particles, with fine texture. At room temperature, it exists stably without special state changes.
When it comes to the melting point, it is about 109-112 ° C. When the temperature gradually rises to this point, the original solid state of 2% 2C4-diethyladipic acid, like ice and snow in the warm sun, slowly melts into a liquid state, which is the key node of the state change.
Its boiling point is quite high, about 328 ° C. When the temperature approaches this value, the liquid 2% 2C4-diethyladipic acid will turn into a gaseous state and rush into space.
Solubility is also an important property. In water, its solubility is very small, like a solitary in water, and it is difficult to blend with water. However, in organic solvents, such as ethanol and ether, it can dissolve well, just like a fish entering water and blending freely.
The density is about 1.06 g/cm ³, which is slightly heavier than water. If placed in water, it will slowly sink.
The physical properties of 2% 2C4-diethyladipic acid are of great significance in many fields such as chemical industry. Due to its characteristics of melting point and boiling point, it can be used as a key reference in synthesis, separation and other processes; its solubility characteristics also have guiding value in solution preparation and reaction medium selection.
Is the chemical properties of 2,4-difluorophenylboronic acid stable?
The chemical properties of 2% 2C4-diethylbenzoic acid are quite stable. Among this compound, the structure of the benzene ring gives it a certain stability. The benzene ring is composed of a conjugated π electron system, and the conjugation effect makes the electron cloud distribution more uniform, which enhances the stability of the molecule.
Furthermore, the ethyl group in the molecule acts as a donor group, providing electrons to the benzene ring through induction effect, further stabilizing the electron cloud structure of the benzene ring. Although the carboxyl group has certain reactivity, under specific conditions, it interacts with other parts of the molecule, which also contributes to the stability of the overall structure.
Under common chemical reaction conditions, if there is a lack of specific reagents and suitable reaction environment, 2% 2C4-diethylbenzoic acid is difficult to undergo significant chemical changes. For example, under extreme conditions such as room temperature and pressure, no strong oxidants, strong acids, and strong bases, it can maintain its own structural integrity.
However, it should be noted that if placed in special environments such as high temperature, strong oxidation or strong reduction, its stability may be affected. High temperature may cause the vibration of chemical bonds in the molecule to intensify. When the energy is sufficient, the chemical bonds may break; strong oxidants can attack benzene rings or carboxyl groups, causing oxidation reactions; strong reducing agents may also change some chemical bond states in the molecule. However, in general, the chemical properties of 2% 2C4-diethylbenzoic acid are relatively stable.
What are the synthesis methods of 2,4-difluorophenylboronic acid?
The synthesis method of 2% 2C4-diethylbenzoic acid is an important topic in the field of organic synthesis. In terms of ancient methods, there are three methods.
First, benzoic acid is used as the starting material to carry out nucleophilic substitution reaction with halogenated ethane under the catalysis of base. In this reaction, the role of base is crucial, which can capture the carboxyl hydrogen of benzoic acid to form benzoate negative ions. This negative ion has strong nucleophilicity and can attack the alpha-carbon of halogenated ethane to form a carbon-carbon bond, resulting in 2% 2C4-diethylbenzoic acid. However, the activity of halogenated ethane must be suitable. If the activity is too high, the side reactions will increase; if the activity is too low, the reaction rate will be delayed. The reaction conditions need to be precisely controlled, and the temperature, time, and amount of alkali will all affect the yield and purity.
Second, through the Fu-gram alkylation reaction. Benzoyl chloride is used as a raw material to first react with Lewis acids such as anhydrous aluminum trichloride to form acyl positive ions, and then alkylate with ethane. In this process, the selection and amount of Lewis acid are crucial, which not only affects the initiation of the reaction, but also affects the selectivity of the reaction. However, the Fu-gram alkylation reaction is prone to polyalkylation side reactions, so measures need to be taken to inhibit it, such as controlling the proportion of reactants, reaction temperature and reaction time, etc., to improve the selectivity of the target product.
Third, with the corresponding phenolic compound as the starting material, the phenolic hydroxyl group is first protected, and then the ethyl group is introduced by the reaction with halogenated ethane, and then the protection is deprotected, and it is converted into benzoic acid through oxidation and other steps. Although this route is slightly complicated, the reaction selectivity of each step is higher, which can effectively avoid the occurrence of side reactions. The protective group of the phenolic hydroxyl group needs to be properly selected, which not only does not affect the subsequent alkylation reaction, but also is easy to remove under suitable conditions. The oxidation step also needs to be careful, and the appropriate oxidant and reaction conditions should be selected to obtain the target product 2% 2C4-diethylbenzoic acid smoothly.
What are the precautions for storing and transporting 2,4-difluorophenylboronic acid?
2% 2C4-diethylbenzoic acid, during storage and transportation, all kinds of precautions are crucial.
First, the control of temperature and humidity is of paramount importance. The nature of this acid is afraid of qualitative change in the presence of high temperature or high humidity. When storing in a cool and dry place, if it is placed in a humid and hot place, it may cause it to decompose and deteriorate, damaging its quality. Therefore, in the warehouse, it is advisable to set up temperature-controlled and moisture-controlled equipment to keep its temperature and humidity in a suitable area.
Second, the packaging must be solid and tight. Because it is corrosive to a certain extent, if the packaging leaks, it will not only damage its own quality, but also endanger the surrounding things and even hurt people. When packaging with corrosion-resistant materials and sealing, it must be tight to prevent leakage. During transportation, attention should also be paid to shock-proof, anti-collision, and packaging damage.
Third, isolated storage, keep in mind. Do not mix with oxidants, strong alkalis and other substances. This acid meets with oxidants, or has a violent chemical reaction, causing the risk of explosion; mixing with strong alkalis can also trigger a reaction and change the properties of the acid. Therefore, in the warehouse, different types of chemicals should be stored in sections with clear labels.
Fourth, fireproof and explosion-proof, should not be ignored. Although this acid is not very flammable and explosive, it still has this risk under specific conditions. In the place of storage and transportation, fireworks are strictly prohibited, and complete fire protection facilities and equipment should be prepared. Personnel should also be familiar with fire protection methods, just in case.
Fifth, the operation norms should not be slack. Whether it is handling, stacking, or loading and unloading during transportation, operators must follow the norms. Wear protective gear, such as gloves, protective clothing, protective glasses, etc., to avoid direct contact and ensure personal safety.