2 4 6 Trifluorotoluene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2,4,6-Trifluorotoluene
Chemical Formula C7H3F3
Molar Mass 146.094 g/mol
Appearance Colorless liquid
Odor Typical aromatic odor
Density 1.247 g/cm³
Boiling Point 107 - 108 °C
Melting Point -45 °C
Flash Point 10 °C
Solubility In Water Insoluble
Vapor Pressure 5.77 kPa at 25 °C
Logp 3.17
Refractive Index 1.4305
FAQ

What are the main uses of 2,4,6-trifluorotoluene?

2%2C4%2C6-%E4%B8%89%E6%B0%9F%E7%94%B2%E8%8B%AF, that is, 2,4,6-triethylbenzene, this substance is an organic compound. Its main use is quite extensive. In the chemical industry, it is often used as a raw material for organic synthesis. Through specific chemical reactions, it can be converted into a variety of high value-added products, such as some fine chemicals, pharmaceutical intermediates, etc. In the field of materials science, it also plays an important role, providing key structural units for the preparation of special performance materials, which helps to improve the specific properties of materials, such as mechanical properties, thermal stability, etc.

The text of Guanfu's "Tiangong Kaiwu" is simple, plain and organized. Today, the answer to this text is as follows:

2,4,6-triethylbenzene, the genus of organic is also. In the field of chemical industry, it is often the material of organic synthesis. With various chemical reactions, it can be transformed into various high-value products, such as fine chemicals and pharmaceutical intermediates. In the science of materials, it is also important to provide the key structural unit for the material of specific properties, and to help the general properties of lifting materials, such as mechanical properties and thermal stability. This material has an indispensable position in the chemical industry and materials industry, and is valued by the industry.

What are the physical properties of 2,4,6-trifluorotoluene?

2%2C4%2C6-%E4%B8%89%E6%B0%9F%E7%94%B2%E8%8B%AF%E7%9A%84%E7%89%A9%E7%90%86%E6%80%A7%E8%B4%A8%E5%A6%82%E4%B8%8B%EF%BC%9A
This substance is also known as trimethylbenzene, which has unique physical characteristics. Looking at its shape, under normal temperature and pressure, it is a colorless, transparent and fragrant liquid, with a strong smell, similar to many organic solvents. To a certain extent, this fragrant smell can be used for some fragrance preparation aids and other purposes.
When it comes to the melting point, the melting point is about -44.7 ° C, and the boiling point is about 164.7 ° C. Such melting boiling point characteristics cause it to exist stably in a liquid state at room temperature, but if the ambient temperature drops below the melting point, it will condense into a solid state. When the temperature rises above the boiling point, it will quickly vaporize into a gaseous state. This property is widely used in chemical separation, purification, etc., by controlling the temperature to achieve the phase transition of substances, and then achieve the purpose of separation from other substances.
In addition to density, its density is about 0.864 g/cm ³, which is lighter than water. If mixed with water, it will float on the water surface. The boundaries between the two are clear. This property plays an important guiding role in some industrial processes and experimental operations involving liquid-liquid separation.
In terms of solubility, it is extremely difficult to dissolve in water, but it can be miscible with most organic solvents such as ethanol, ether, benzene, etc. in any ratio. This solubility property is widely used in the field of organic synthesis. It is often used as an excellent solvent to help chemical reactions proceed smoothly, providing a compatible environment for various organic compounds, enabling more complete contact between reactants and accelerating the reaction process.

Is the chemical properties of 2,4,6-trifluorotoluene stable?

The chemical properties of 2% 2C4% 2C6-tribromotoluene are still stable. In this compound, the bromine atom is connected to the benzene ring, and the structure of the benzene ring gives it a certain stability.

The benzene ring has a conjugated π electron system, and the electron cloud is uniformly distributed and delocalized, which stabilizes the molecular structure. Although the bromine atom has a certain electronegativity and can absorb electron induction effect, it also has a donor electron conjugation effect. The donor electron conjugation effect interacts with the benzene ring conjugation system to maintain the stability of the overall electron cloud distribution of the molecule to a certain extent.

Under normal conditions, 2% 2C4% 2C6-tribromotoluene is not prone to spontaneous chemical reactions. Under the action of general ambient temperature and common chemical reagents, its chemical properties are stable, and it is not easy to decompose or react quickly with other substances.

However, it needs to be noted that if it is under certain extreme conditions, such as high temperature, strong oxidants or the presence of special catalysts, its stability may be affected. High temperature can provide enough energy to break the chemical bonds in the molecule and promote the reaction to occur; strong oxidants can oxidize with certain groups in the molecule and change its chemical structure.

In summary, under conventional conditions, 2% 2C4% 2C6 -tribromotoluene is chemically stable, but under special extreme conditions, its stability may change.

What are the preparation methods of 2,4,6-trifluorotoluene?

In the case of 2% 2C4% 2C6-tribromotoluene, there are several ways to make it.

One method is to use toluene as a base to interact with a brominating agent. Toluene is added to a suitable device, bromine is added, and a suitable catalyst is added, such as iron powder. When bromine meets toluene, it undergoes a substitution reaction, and the bromine atom gradually enters the toluene ring, resulting in 2% 2C4% 2C6-tribromotoluene. However, this reaction requires careful control of its temperature and the amount of bromine. If the temperature is too high, the side reaction will be complicated and impure; too much or too little bromine will hinder the yield and purity.

The second method is to first derive toluene from other groups that are easy to react with bromine. For example, toluene is nitrified first to obtain nitrotoluene. The nitro group is a blunt group, which can lead bromine atoms into specific positions. After that, the nitro group is reduced to an amino group, and the amino group is an active group with strong localization. At this time, it reacts with bromine, and the bromine atom adds 2% 2C4% 2C6 position. Finally, after a series of reactions such as diazotization, the amino group is removed, and 2% 2C4% 2C6-tribromotoluene can be obtained. Although the steps in this way are slightly complicated, the entry of bromine atoms can be better controlled, and the purity of the product can be obtained. < Br >
There are other compounds containing benzene ring as the beginning, through a series of reactions, converted into toluene, and then according to the above method of 2% 2C4% 2C6 -tribromotoluene. The process may involve the construction of carbon chains, the conversion of groups, etc. All these methods have advantages and disadvantages. According to the actual situation, such as the availability of raw materials, the purity of the product, and the consideration of cost, choose the appropriate one and use it.

What are the precautions for storing and transporting 2,4,6-trifluorotoluene?

2% 2C4% 2C6-tribromotoluene is also an organic compound. During storage and transportation, many matters must be paid attention to.

First, when storing, choose a cool and ventilated warehouse. This is because 2% 2C4% 2C6-tribromotoluene is easily decomposed when heated, causing danger. The temperature of the warehouse should be controlled in a specific range, and it must be kept away from fire and heat sources to prevent unexpected fires.

Second, it should be stored separately from oxidants and food chemicals. Cover 2% 2C4% 2C6-tribromotoluene in case of oxidizing agent, easy to cause violent chemical reaction, or risk of explosion and combustion; mixed with edible chemicals, it may contaminate food and endanger human life and health.

Third, the storage place should be prepared with suitable materials to contain leaks. In case of leakage, it can be collected in time to prevent its spread and environmental pollution.

As for transportation, the transportation vehicle must ensure that the vehicle is in good condition and have corresponding safety measures. During transportation, it should also be protected from exposure to the sun, rain and high temperature. When loading and unloading, the operation must be light and light, so as not to damage the packaging container. If the package is damaged, 2% 2C4% 2C6-tribromotoluene will leak, which will not only pollute the environment but also pose a danger.

In addition, transportation personnel should also be professionally trained to be familiar with the characteristics and emergency treatment methods of 2% 2C4% 2C6-tribromotoluene. In case of emergency, it can be disposed of quickly and properly to reduce the damage. In this way, in the storage and transportation of 2% 2C4% 2C6-tribromotoluene, act with caution, and the security will be safe.