2 4 5 6 Tetrafluorobenzene 1 3 Dicarbonitrile
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2,4,5,6-tetrafluorobenzene-1,3-dicarbonitrile
Chemical Formula C8H2F4N2
Molar Mass 202.109 g/mol
Appearance Solid (Typically)
Melting Point Data specific to this compound needed
Boiling Point Data specific to this compound needed
Density Data specific to this compound needed
Solubility In Water Low (Expected due to non - polar nature of benzene ring and hydrophobic fluorine groups)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (Expected based on structure)
Purity Varies by production method and grade
Flash Point Data specific to this compound needed
Refractive Index Data specific to this compound needed
Chemical Formula C8H2F4N2
Molar Mass 202.109 g/mol
Appearance Solid (usually white or off - white)
Melting Point Data specific to the compound (check relevant literature)
Boiling Point Data specific to the compound (check relevant literature)
Density Data specific to the compound (check relevant literature)
Solubility In Water Low (organic compound, non - polar nature)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Low (due to its solid state at room temperature)
Stability Stable under normal conditions, may react with strong oxidizing or reducing agents
Chemical Formula C8H2F4N2
Molar Mass 202.11 g/mol
Appearance Solid (likely white or off - white powder)
Physical State At Room Temperature Solid
Boiling Point Data may vary, but generally high due to strong intermolecular forces
Melting Point Specific value depends on purity, typically in a certain temperature range
Solubility In Water Low solubility, as it is a non - polar aromatic compound
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Density Density value would be determined experimentally and is characteristic of the compound
Odor May have a faint, characteristic odor
FAQ

What is the main use of 2,4,5,6 - tetrafluorobenzene - 1,3 - dicarbonitrile

2% 2C4% 2C5% 2C6 - tetrafluorobenzene - 1% 2C3 - dicarbonitrile, Chinese name 2,4,5,6 - tetrafluorobenzene, this substance is widely used.

In the field of material synthesis, its importance is significant. Because of its fluorine atom and cyanide group, it can be used as a key monomer to prepare high-performance polymers. Taking the preparation of fluorinated polyimide as an example, 2,4,5,6 - tetrafluorobenzene participates in the reaction, which can endow polyimide materials with excellent characteristics. The introduction of fluorine atoms can reduce the surface energy of the polymer and improve its chemical corrosion resistance and weather resistance; cyanide groups can participate in the crosslinking reaction to enhance the mechanical properties and thermal stability of the material. In the field of aerospace, this polymer can be used to make aircraft structural components. With its light weight, high strength and high stability, it can meet the strict requirements of aircraft. In the field of electronics, it can be used as an insulating material for printed circuit boards. Its good insulation and thermal stability ensure the stable operation of electronic equipment.

In organic synthetic chemistry, 2,4,5,6-tetrafluoroisophthalonitrile is an important intermediate. Cyanyl groups can be converted through a variety of chemical reactions, such as hydrolysis to form carboxyl groups, and then tetrafluoroisophthalic acid can be synthesized, which is widely used in the synthesis of medicine and pesticides. At the same time, cyanyl groups can also participate in reactions such as nucleophilic addition and cyclization to synthesize organic compounds with diverse structures, providing possibilities for the development of new drugs and functional materials.

In the field of dyes, 2,4,5,6-tetrafluoroisophthalonitrile also has application potential. Its unique molecular structure and fluorine atomic properties can be used to synthesize new fluorine-containing dyes. Fluorine-containing dyes usually have the advantages of bright color, good light resistance and washing resistance, and have broad application prospects in the textile printing and dyeing industry. They can be used for high-end textile dyeing to improve textile quality and added value.

What are the physical properties of 2,4,5,6 - tetrafluorobenzene - 1,3 - dicarbonitrile

2%2C4%2C5%2C6+-+tetrafluorobenzene+-+1%2C3+-+dicarbonitrile, the Chinese name may be 2,4,5,6-tetrafluorobenzene-1,3-dinitrile. The physical properties of this substance, let me tell you.

Looking at its appearance, under normal temperature and pressure, it is often in the state of white to light yellow crystalline powder. The characteristics of this color state may help to identify this substance among many things.

The melting point is about 115-119 ° C. When the ambient temperature rises to this value, the substance gradually melts from the solid state to the liquid state. The temperature of this phase transition is one of its important physical properties.

As for the boiling point, under specific pressure conditions, it can reach a certain value. However, due to the lack of precise external conditions, the exact boiling point is difficult to state. However, it can be seen that the boiling point is affected by pressure, and the boiling point varies depending on the pressure.

In terms of solubility, it has a certain solubility in organic solvents, such as common N, N-dimethylformamide (DMF), dichloromethane, etc. This characteristic makes it possible to dissolve it in these organic solvents in chemical synthesis or related experiments to participate in various reactions. In water, its solubility is very small, because water is a solvent with strong polarity, and the polarity of the substance is relatively weak, according to the principle of "similar miscibility", it is difficult to dissolve in water.

Density is also one of its physical properties. Although the exact value is not known in detail, its density may be different from that of common organic solvents. When it comes to mixing, separation and other operations, the density is also valuable to consider.

In addition, although the physical properties such as vapor pressure of the substance are not yet clear, in chemical production, storage and other links, vapor pressure is related to the degree of volatilization of the substance, which is also a factor that cannot be ignored.

The physical properties of
2,4,5,6-tetrafluorobenzene-1,3-dinitrile, such as appearance, melting point, solubility, etc., are of great significance in the research and production operations of chemical industry and materials, and can help practitioners to use this substance rationally and achieve the desired purpose.

What is the synthesis method of 2,4,5,6 - tetrafluorobenzene - 1,3 - dicarbonitrile

2% 2C4% 2C5% 2C6 - tetrafluorobenzene - 1% 2C3 - dicarbonitrile, that is, 2,4,5,6 - tetrafluoro-isophthalonitrile, is synthesized as follows:

To prepare 2,4,5,6 - tetrafluoro-isophthalonitrile, it can be achieved by a suitable starting material through several steps of reaction. Usually starting with a compound containing a benzene ring and a suitable substituent.

One method can first take a benzene derivative containing a specific substituent and react with a reagent capable of introducing a cyanyl group to obtain a benzene compound containing a cyanide group. In this process, suitable reaction conditions, such as specific temperature, pressure and catalyst, need to be selected to promote the effective introduction of cyanide groups. For example, with a halogenated benzene derivative and a cyanide reagent, under the action of an appropriate organic solvent and catalyst, the reaction is heated, and the halogen atom is replaced by a cyanide group through nucleophilic substitution.

Then, the obtained cyanide-containing benzene compound is introduced into the fluorine atom. In this step, fluorination reagents are commonly used, and under specific reaction conditions, fluorine atoms are substituted for hydrogen atoms at specific positions on the benzene ring. The fluorination reaction needs to be finely regulated. Due to the special reactivity of fluorine atoms, improper reaction conditions can easily lead to side reactions. For example, a suitable fluorinating agent is selected, and under low temperature or mild heating conditions, the reaction process is controlled, and gradually the four hydrogen atoms on the benzene ring are replaced by fluorine atoms, and finally 2,4,5,6-tetrafluoro-isophthalonitrile is obtained. < Br >
Or first fluorinate the benzene ring to obtain fluorobenzene derivatives, and then introduce cyanide groups through cyanidation. This path also requires careful selection of reaction conditions at each step to ensure that the reaction proceeds in the predetermined direction and improves the yield and purity of the product. In short, the key to synthesizing this compound lies in the precise control of the reaction conditions at each step and the rational design of the reaction path.

2,4,5,6 - tetrafluorobenzene - 1,3 - dicarbonitrile What are the precautions in storage and transportation

2% 2C4% 2C5% 2C6 - tetrafluorobenzene - 1% 2C3 - dicarbonitrile is 2,4,5,6 - tetrafluoroisophthalonitrile. When storing and transporting this substance, all precautions should not be ignored.

Its properties are chemical substances. When storing, the first environment is dry and cool. Do not expose to direct sunlight, nor near fire and heat sources to prevent it from being unstable due to changes in temperature. High temperature can easily lead to chemical reactions, or increase the internal pressure of the packaging container, causing the risk of rupture.

Furthermore, the storage place must be well ventilated. Good ventilation can prevent the accumulation of harmful gases and ensure environmental safety. And should be placed separately from oxidizing agents, acids, alkalis and other substances. Due to its active chemical properties, contact with other substances, or violent reaction, causing danger.

As for transportation, it must be strictly implemented in accordance with relevant laws and regulations. The selected means of transportation should be clean and free of other chemicals to avoid cross-contamination. During transportation, the escort must strictly guard the post and pay close attention to the condition of the goods. In case of bumps, collisions, etc., dispose of it in time to avoid package damage and material leakage.

If the package is accidentally damaged, emergency measures should be taken immediately. Evacuate the surrounding crowd, isolate the contaminated area, and do not let unrelated people approach. Emergency personnel must wear professional protective equipment, properly collect leaked materials, and dispose of them in accordance with relevant regulations to prevent them from entering the environment and harming the ecology. In this way, 2,4,5,6-tetrafluoroisophthalonitrile is guaranteed to be safe during storage and transportation.

2,4,5,6 - tetrafluorobenzene - 1,3 - what is the market outlook for dicarbonitrile

2%2C4%2C5%2C6+-+tetrafluorobenzene+-+1%2C3+-+dicarbonitrile is 2,4,5,6-tetrafluorobenzene-1,3-dinitrile, which has its specific market prospect in the field of chemical materials.

The market of Guanfu 2,4,5,6-tetrafluorobenzene-1,3-dinitrile has a promising future. In the field of electronic materials, with the development of electronic devices to be light, short, and high-performance, the demand for special functional materials is increasing. This compound can be used to prepare high-performance electronic packaging materials, liquid crystal display materials, etc. because of its unique molecular structure and properties. Today's electronics industry is booming, and there is a constant need for new materials. Therefore, it must have a place in the electronic materials market and is expected to expand its application with the development of the industry.

Furthermore, in the field of pharmaceutical and chemical industry, it may be a key intermediate for the synthesis of new drugs. Pharmaceutical research and development is constantly pursuing new targets and new structural drugs. The special structure of 2,4,5,6-tetrafluorobenzene-1,3-dinitrile may provide pharmaceutical chemists with novel synthesis ideas and structural templates. Nowadays, the pharmaceutical market is huge and continues to grow, and the demand for characteristic intermediates is also rising. This compound also has potential opportunities in the pharmaceutical and chemical market.

However, its market development is not smooth. The process of synthesizing this compound may be complicated and costly. If it is to be widely used, it is necessary to optimize the synthesis route and reduce production costs. And the market competition is fierce, and similar or alternative materials also pose challenges. Only by continuously improving technology and improving product quality and cost performance can we stand out in the market and enjoy the benefits of the future.