Chemical Formula | C6H4F2 |
Molecular Weight | 114.09 |
Appearance | Colorless liquid |
Odor | Aromatic odor |
Boiling Point | 88 - 89 °C |
Melting Point | -53.1 °C |
Density | 1.165 g/mL at 25 °C |
Solubility In Water | Insoluble |
Vapor Pressure | 14.6 mmHg at 25 °C |
Flash Point | -12 °C |
Refractive Index | 1.4256 at 20 °C |
Chemical Formula | C6H4F2 |
Molar Mass | 114.092 g/mol |
Appearance | Colorless liquid |
Odor | Aromatic odor |
Density | 1.163 g/cm³ at 20 °C |
Boiling Point | 88 - 90 °C |
Melting Point | -24 °C |
Solubility In Water | Insoluble |
Vapor Pressure | 13.3 kPa at 22.5 °C |
Flash Point | -12 °C |
Chemical Formula | C6H4F2 |
Molar Mass | 114.09 g/mol |
Appearance | Colorless liquid |
Odor | Characteristic aromatic odor |
Density | 1.165 g/cm³ (at 20 °C) |
Boiling Point | 88 - 89 °C |
Melting Point | -53.1 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in many organic solvents |
Vapor Pressure | 10.7 kPa at 25 °C |
Flash Point | -12 °C |
Refractive Index | 1.429 (at 20 °C) |
What are the main uses of p-Difluorobenzene?
P-difluorobenzene is also an organic compound. It has a wide range of uses and has important applications in various fields of chemical industry.
First, it is often a key intermediate in the synthesis of medicine. Pharmaceutical developers rely on its special chemical structure to build complex drug molecules. Because it can give drugs specific properties, such as improving the solubility, stability and biological activity of drugs. For example, when synthesizing some new antibacterial drugs, p-difluorobenzene participates in the reaction, helping to form a drug structure with a unique antibacterial mechanism, adding a weapon for human beings to fight diseases.
Second, in the field of materials science, it also has important functions. Can be used to prepare high-performance polymer materials. By polymerizing with other monomers, the heat resistance, chemical corrosion resistance and mechanical properties of the polymer can be improved. For example, the addition of p-difluorobenzene to special plastics required in the manufacturing of aerospace fields enables the material to adapt to extreme environments and ensure the safe and stable operation of aircraft.
Third, in electronic chemicals, p-difluorobenzene is also indispensable. In the semiconductor manufacturing process, some photoresists and electronic packaging materials need to be prepared as raw materials. Because it helps to improve the performance and reliability of electronic components, meet the increasingly advanced needs of electronic products, and promote the rapid development of electronic technology.
In conclusion, although p-difluorobenzene is an organic compound, it plays a pivotal role in many key fields such as medicine, materials, and electronics, and has made significant contributions to human life and technological progress.
What are the physical properties of p-Difluorobenzene?
P-difluorobenzene is also an organic compound. Its physical properties are unique, let me explain in detail for you.
First of all, at room temperature, p-difluorobenzene is in the state of a colorless liquid, clear and transparent, like a clear spring, giving people a sense of purity.
As for its smell, it has an aromatic smell. However, this fragrance is not an ordinary rich fragrance, but a unique and elegant fragrance, which is unique in smell.
The boiling point is about 83 ° C. The value of this boiling point determines that it can be converted from liquid to gas at a certain temperature. When the temperature gradually rises to about 83 ° C, p-difluorobenzene molecules obtain enough energy to break free from the attractive force between them and dissipate into gaseous state.
Its melting point is -13.2 ° C. At lower temperatures, p-difluorobenzene will solidify into a solid state, and the molecular arrangement is more orderly, showing the characteristics of a solid state.
p-difluorobenzene has a slightly smaller density than water, about 1.15g/cm ³. If it is placed in one place with water, it can be seen that it floats on the water surface, like a light boat floating in blue waves.
In terms of solubility, p-difluorobenzene is insoluble in water. The polarity of water is significantly different from the non-polar structure of p-difluorobenzene. According to the principle of "similarity and miscibility", the two are difficult to dissolve with each other. However, it is soluble in many organic solvents, such as ethanol and ether, which can be uniformly dispersed to form a uniform solution system.
In addition, the vapor pressure of p-difluorobenzene also has a certain value at a specific temperature, which is related to its equilibrium state between the gas phase and the liquid phase, and affects its volatilization degree in practical application scenarios. Its vapor density is greater than that of air. If it evaporates in an open environment, the steam will spread close to the ground. Please pay attention to relevant safety matters. All these physical properties play a key role in the application of chemical engineering, medicine and many other fields, laying the foundation for their participation in various reactions and specific effects.
Is p-Difluorobenzene chemically stable?
The chemical properties of p-difluorobenzene are quite stable. The reason is that its molecular structure is unique. The benzene ring is a conjugated system with high stability, the electron cloud is evenly distributed, and it is not easy to be attacked by external reagents. The fluorine atom is connected to the benzene ring. Although the fluorine electronegativity is extremely high and has a strong electron-absorbing induction effect, the p-π conjugation effect formed by it and the benzene ring cancels part of the electron-absorbing effect to a certain extent, so that the electron cloud density of the benzene ring does not decrease excessively.
The existence of this conjugated system makes p-difluorobenzene less prone to electrophilic substitution reactions. To make such reactions occur, more severe conditions are required, such as high temperature and catalysts. And even if it reacts, its reactivity is lower than that of benzene.
Furthermore, the carbon-fluorine bond in p-difluorobenzene has a high bond energy. The radius of the fluorine atom is small, and the covalent bond formed with the carbon atom is short and strong, which is difficult to break. This is also an important factor for its chemical stability. Even in the face of common oxidizing and reducing agents, it is difficult for p-difluorobenzene to react significantly with it without specific conditions.
In summary, the properties of the conjugated structure of the p-difluorobenzene benzene ring and the carbon-fluorine bond are relatively stable, and it is not easy to participate in various chemical reactions under common conditions.
What are the preparation methods of p-Difluorobenzene?
P-dichlorobenzene is also an organic compound. The method of its preparation used to follow various paths in the past.
First, it can be started from p-dichlorobenzene. Under specific reaction conditions, p-dichlorobenzene and potassium fluoride can undergo a halogen exchange reaction. This reaction often needs to be carried out in an organic solvent and accompanied by an appropriate catalyst, such as crown ethers. Crown ethers can increase the solubility of potassium fluoride in organic solvents, making the reaction easier to occur. During the reaction, temperature is also a key factor. Generally, it needs to be maintained at a certain high temperature range, so that the chlorine atoms of p-dichlorobenzene are gradually replaced by fluorine atoms, so that p-dichlorobenzene can be prepared.
Second, benzene is used as the starting material. First, benzene is nitrified to obtain nitrobenzene. Nitrobenzene can be converted into aniline after reduction. Aniline interacts with sodium nitrite and hydrofluoric acid to form diazonium salts, which are thermally decomposed, and fluorine atoms replace amino groups to obtain fluorobenzene derivatives. After further reaction and purification, p-difluorobenzene can also be obtained. Although this process is slightly complicated, it is a commonly used method in organic synthesis strategies.
Third, it is prepared from corresponding phenolic compounds. Phenolic compounds are halogenated, halogen atoms are introduced, and then fluorinated, and fluorine atoms are replaced by halogen atoms, thus achieving the purpose of preparing p-difluorobenzene. This approach requires attention to the control of reaction conditions. Due to the high activity of phenolic compounds, the reaction is prone to side reactions. Therefore, in each step of the reaction, fine regulation is required to ensure the purity and yield of the product.
What is the price range of p-Difluorobenzene in the market?
In today's world, business conditions are ever-changing, and the price of p-difluorobenzene in the market also fluctuates for many reasons, making it difficult to determine. Its price often changes due to the abundance of raw materials, the situation of supply and demand, the difficulty of craftsmanship, and the guidance of government orders.
Looking at the past, if raw materials are widely available and easy to obtain, the process is becoming simpler, resulting in an increase in output, and the price may decline; however, if raw materials are scarce, the demand is too high for supply, and the price must rise. And the regulations of the government have a great impact, or the promotion of production, or the restriction of production, all make the price change differently.
If you want to know the exact price, you should ask the platform for chemical product trading, the broker in the industry, and the merchant specializing in it. They have the latest business information and can tell the current price. Or based on recent market conditions, the rough estimate of the price is between [X1] yuan and [X2] yuan per kilogram, but this is only speculation, and the truth must be subject to real-time.