M Difluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
m-Difluorobenzene
Chemical Formula C6H4F2
Molar Mass 114.09 g/mol
Appearance Colorless liquid
Odor Aromatic odor
Density 1.157 g/cm³ at 20 °C
Boiling Point 112 - 114 °C
Melting Point -57 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in many organic solvents
Flash Point 12 °C
Vapor Pressure 5.33 kPa at 25.7 °C
Refractive Index 1.4586 at 20 °C
Chemical Formula C6H4F2
Molar Mass 114.09 g/mol
Appearance Colorless liquid
Odor Aromatic odor
Density 1.155 g/cm³ at 20 °C
Boiling Point 88 - 90 °C
Melting Point -57.4 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents
Flash Point -5 °C
Vapor Pressure 4.8 kPa at 25 °C
Refractive Index 1.454 at 20 °C
Chemical Formula C6H4F2
Molar Mass 114.09 g/mol
Appearance Colorless liquid
Odor Characteristic aromatic odor
Density 1.159 g/cm³ at 20 °C
Boiling Point 112 - 114 °C
Melting Point -57.3 °C
Solubility In Water Insoluble
Vapor Pressure 3.65 kPa at 25 °C
Flash Point 12 °C
FAQ

What are the main uses of m-Difluorobenzene?

M-difluorobenzene is an organic compound with a wide range of uses.

In the field of pharmaceutical synthesis, this is an important intermediate. The preparation of many drugs relies on it as a starting material, which is converted into substances with specific pharmacological activities through multi-step reactions. For example, some antidepressants and drugs for the treatment of cardiovascular diseases, m-difluorobenzene plays a key role in its synthesis route, which can endow drugs with specific spatial structures and chemical properties to meet the needs of human targets.

It is also an indispensable ingredient in the manufacture of pesticides. With its chemical properties, high-efficiency, low-toxicity and environmentally friendly pesticides can be synthesized. Such pesticides are highly lethal to pests, but less harmful to the environment and non-target organisms. For example, in the development of some new insecticides and fungicides, m-difluorobenzene is involved to optimize the performance of pesticides and improve the yield and quality of crops.

In the field of materials science, m-difluorobenzene also shows unique value. It can be used to prepare high-performance polymer materials, such as fluoropolymer materials. Such materials have excellent thermal stability, chemical stability and electrical properties, and are widely used in high-end fields such as electronics and aerospace. For example, in electronic chip packaging materials and structural components of aerospace devices, fluoropolymer materials rely on their excellent characteristics to ensure stable operation of equipment.

In addition, in the field of dye synthesis, m-difluorobenzene is used as a raw material to endow dyes with unique color and fastness. After a specific chemical reaction, it is introduced into the molecular structure of dyes to improve the affinity and dyeing effect of dyes to fibers, meeting the needs of high-quality dyes in textile, printing and dyeing industries.

What are the physical properties of m-Difluorobenzene?

M-difluorobenzene is an organic compound. It has special physical properties and is listed below:
- ** Properties **: Colorless and transparent liquid, clear in appearance, good light transmittance, and no impurities visible to the naked eye. At room temperature and pressure, maintain a liquid state, which is stable and easy to store and transport.
- ** Melting point **: about -57.3 ° C. When the temperature drops to this point, m-difluorobenzene gradually changes from liquid to solid state, and the molecular movement slows down, and the arrangement tends to be orderly.
- ** Boiling point **: about 88.6 ° C. When the temperature rises to the boiling point, m-difluorobenzene absorbs enough energy, and the molecules break free from the liquid phase and transition into a gaseous state to escape. < Br > - ** Density **: 1.129g/cm ³ (20 ° C), slightly heavier than water. If it is mixed with water, it will sink to the bottom of the water, which is of great significance in the separation and extraction process.
- ** Solubility **: It is difficult to dissolve in water, because it is a non-polar organic matter, and water is a polar solvent. According to the principle of "similar miscibility", the two have poor miscibility. However, m-difluorobenzene can be miscible with most organic solvents, such as ethanol, ether, acetone, etc., and is often used as a solvent in organic synthesis reactions.
- ** Vapor pressure **: At a specific temperature, when the steam of m-difluorobenzene reaches equilibrium with the liquid phase, the pressure of the steam is the vapor pressure. Vapor pressure is related to temperature. When temperature increases, vapor pressure increases, and volatility increases. When storing and using, pay attention to ventilation to prevent vapor accumulation.
- ** Refractive index **: about 1.446 (20 ° C), this parameter reflects the degree of refraction of light when passing through m-difluorobenzene, and can be used for identification and purity analysis.

What are the chemical properties of m-Difluorobenzene?

M-difluorobenzene is also an organic compound. Its molecule contains difluorine atoms connected to the interposition of the benzene ring. This substance has unique chemical properties and is widely used in organic synthesis and other fields.

Looking at its physical properties, m-difluorobenzene is a colorless and transparent liquid with a fragrant odor at room temperature and pressure. Its boiling point is about 112-113 ° C, the melting point is -57.4 ° C, and its density is lighter than water, about 1.116 g/cm ³. It is insoluble in water and can be miscible with organic solvents such as ethanol and ether.

In terms of its chemical properties, the conjugated system of the benzene ring gives it stability, but the introduction of fluorine atoms makes it have special activity. Fluorine atoms have strong electronegativity, which can change the electron cloud density of the benzene ring and affect the electrophilic substitution reaction.

In the electrophilic substitution reaction, the electron cloud density of the benzene ring decreases due to the electron-absorbing induction effect of the fluorine atom, and the reactivity is slightly lower than that of benzene. However, the electron cloud density of the ortho and para-position is slightly higher than that of the relative meta-position, and the electrophilic reagents are more likely to attack the ortho and para-position. However, due to the combined effect of steric resistance and electronic effect, the meta-substitution products can also be obtained.

m-difluorobenzene can also participate in the coupling reaction catalyzed by metals. Under the action of metal catalysts such as palladium and nickel, the fluorine atoms can be coupled with nucleophiles containing carbon, nitrogen, and oxygen to form carbon-carbon and carbon-heteroatom bonds, which is of great significance in the fields of drug synthesis and material preparation.

And because of its fluorine content, m-difluorobenzene exhibits certain chemical stability and biological activity. In pharmaceutical chemistry, fluorine-containing groups are often introduced to change the lipophilicity, metabolic stability and biological activity of compounds, so m-difluorobenzene is an important intermediate in drug synthesis.

What is the production method of m-Difluorobenzene?

M-difluorobenzene is also an organic compound. There are several common methods for its preparation.

First, m-phenylenediamine is used as the starting material. First, m-phenylenediamine reacts with hydrofluoric acid and sodium nitrite, and conducts a diazotization reaction. In the meantime, sodium nitrite reacts with hydrofluoric acid to form nitrous acid, and nitrous acid reacts with the amino group in m-phenylenediamine to form a diazo salt. This diazo salt is unstable. When heated or in contact with appropriate reagents, fluorine ions replace the diazo group, and m-difluorobenzene is obtained. This way, attention should be paid to the control of reaction conditions. Temperature and pH are both critical. If the temperature is too high, the diazo salt is easy to decompose, resulting in impure products; if the pH is not suitable, the < Br >
Second, starting from m-bromofluorobenzene. M-bromofluorobenzene interacts with metal magnesium to form Grignard's reagent. After reacting with fluorinated reagents, such as boron trifluoride ether complexes, the bromine atom is replaced by a fluorine atom to obtain m-difluorobenzene. In this process, the preparation of Grignard's reagent requires an anhydrous environment, otherwise the Grignard's reagent is prone to hydrolysis and failure. And when reacting with fluorinated reagents later, it is also necessary to pay attention to the reaction time and temperature to promote the reaction to generate m-difluorobenzene.

Third, m-dichlorobenzene is used as the raw material. In the presence of specific solvents and catalysts, m-dichlorobenzene and potassium fluoride undergo halogen exchange The choice of solvent is important, and it needs to be able to dissolve the reactants without adverse effects on the reaction, such as N-methylpyrrolidone. Catalysts can speed up the reaction rate, and copper salts are commonly used. This reaction condition is more harsh, and high temperature and high pressure are required to make the reaction fully occur to obtain the target product m-difluorobenzene.

What should be paid attention to when storing and transporting m-Difluorobenzene?

M-difluorobenzene is also an organic compound. It is necessary to be careful when storing and transporting it.

When hiding, the first environment. It should be placed in a cool and ventilated storage. Keep away from fire and heat sources, and the storage temperature should not exceed 37 ° C. Because of its flammability, it can be burned in case of open flames and hot topics, so fire prevention is essential. In addition, it should be stored in separate stores with oxidants and acids. Do not mix storage to prevent their interaction and danger. The storage area should be equipped with suitable materials to contain leaks.

When transporting, pay more attention. Vehicles need to be equipped with corresponding varieties and quantities of fire equipment and leakage emergency treatment equipment. It is best to transport in the morning and evening in summer to avoid high temperature periods. The trough (tank) car used during transportation should have a grounding chain, and holes can be set in the trough to baffle to reduce shock and generate static electricity. Mixed transportation with oxidants, acids, etc. is strictly prohibited. During transportation, it should be protected from exposure to the sun, rain, and high temperature. During stopovers, it should be kept away from fires, heat sources, and high temperature areas. Vehicle exhaust pipes must be equipped with fire retardant devices, and it is forbidden to use mechanical equipment and tools that are prone to sparks for loading and unloading. Highway transportation should be carried on the prescribed route, and do not stop in residential areas and densely populated areas. It is forbidden to slip during railway transportation.

In this way, the possession and transportation of m-difluorobenzene will be safe