1 Bromo 2 Chloro 3 4 Difluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-Bromo-2-chloro-3,4-difluorobenzene
Chemical Formula C6H2BrClF2
Appearance Liquid (usually)
Physical State At Room Temperature Liquid
Boiling Point Data needed
Melting Point Data needed
Density Data needed
Solubility In Water Low solubility
Solubility In Organic Solvents Soluble in common organic solvents
Vapor Pressure Data needed
Flash Point Data needed
Odor Characteristic aromatic odor (presumed)
Chemical Formula C6H2BrClF2
Appearance Colorless to light yellow liquid
Boiling Point Approximately 195 - 200 °C
Density Around 1.8 g/cm³ (estimated)
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Vapor Pressure Low at room temperature
Chemical Formula C6H2BrClF2
Molecular Weight 229.43
Appearance Colorless to light yellow liquid
Boiling Point 185 - 187 °C
Melting Point N/A
Density 1.77 g/cm³
Solubility Insoluble in water, soluble in organic solvents
Vapor Pressure Low
Flash Point 78 °C
Refractive Index 1.535 - 1.537
FAQ

What are the main uses of 1-Bromo-2-chloro-3,4-difluorobenzene?

1-Bromo-2-chloro-3,4-difluorobenzene is a kind of organic compound. Its main use involves the field of organic synthesis.

In the synthesis of medicine, this compound is often a key intermediate. Because of its halogen atoms, it can introduce other functional groups through various reactions such as nucleophilic substitution, and then build complex drug molecules. For example, it can be used to synthesize anti-infective drugs with specific physiological activities. By virtue of its structural properties, it can be combined with specific targets of pathogens to achieve therapeutic effect.

In the process of pesticide creation, 1-bromo-2-chloro-3,4-difluorobenzene is also indispensable. It can be made into highly efficient and low-toxic pesticides through a series of chemical transformations. Its special molecular structure may give pesticides excellent insecticidal, bactericidal or weeding properties, and has little impact on the environment, which is in line with the current needs of green agriculture development.

Furthermore, in the field of materials science, it can also be seen. Or it can be used to synthesize special polymer materials, such as polymers with special electrical and optical properties. Through the reaction caused by its halogen atoms, the molecular structure and properties of polymers can be precisely regulated to meet the needs of specific fields such as electronic devices and optical materials.

In summary, 1-bromo-2-chloro-3,4-difluorobenzene, with its unique chemical structure, has shown important uses in many fields such as medicine, pesticides and materials, promoting the sustainable development and progress of related industries.

What are the physical properties of 1-Bromo-2-chloro-3,4-difluorobenzene?

1-Bromo-2-chloro-3,4-difluorobenzene is one of the organic compounds. Its physical properties are well-researched.

When it comes to appearance, under room temperature and pressure, it often takes the form of a colorless to light yellow liquid. It is quite fluid in appearance, with a warm luster and a clear oily liquid.

As for the smell, it often emits a special aromatic smell, but this smell is by no means pleasant. The smell is pungent and has a significant stimulation to the olfactory nerve. If people are close to it, it is very easy to detect its strong smell.

Its boiling point is also an important physical property. In a specific pressure environment, 1-bromo-2-chloro-3,4-difluorobenzene has a fixed boiling point. This boiling point value varies slightly depending on the external pressure, but the approximate range can be found. It usually boils within a certain temperature range. This characteristic is crucial in the process of separation and purification.

Melting point cannot be ignored. During the cooling process, the substance gradually turns from liquid to solid state, and 1-bromo-2-chloro-3,4-difluorobenzene realizes this phase transition at a certain temperature. This melting point is its inherent property and can be used to identify the substance.

In terms of solubility, the solubility of this compound in water is very small. If the two are mixed, the appearance of stratification can be observed. 1-Bromo-2-chloro-3,4-difluorobenzene floats on water, like oil and water, distinct. However, it has good solubility in organic solvents, such as common ethanol, ether, acetone, etc., and can be miscible with these organic solvents to form a uniform solution system.

Density, 1-bromo-2-chloro-3,4-difluorobenzene has a higher density than water, so when mixed with water, it sinks underwater. This density property has practical value in many chemical operations, material separation, etc.

The above are all important physical properties of 1-bromo-2-chloro-3,4-difluorobenzene, which are indispensable factors in chemical production, scientific research and other fields.

What is the chemical synthesis method of 1-Bromo-2-chloro-3,4-difluorobenzene?

The chemical synthesis of 1-bromo-2-chloro-3,4-difluorobenzene follows the techniques and principles of organic synthesis. The following is a possible way to synthesize this compound:

Starting material, optionally based on o-difluorobenzene. The capped o-difluorobenzene has a specific electron cloud distribution and reactivity, which is conducive to the development of subsequent reactions.

The first step can halogenate o-difluorobenzene with a chlorine source. Commonly used chlorine sources, such as chlorine gas ($Cl_2 $), in the presence of suitable catalysts, such as ferric chloride ($FeCl_3 $), will introduce chlorine atoms into the benzene ring of o-difluorobenzene. This reaction follows the mechanism of electrophilic substitution reaction. Due to the electron-rich properties of the benzene ring, it is susceptible to attack by electrophilic reagents. Under the action of ferric chloride, chlorine generates a cation of chlorine ($Cl ^ + $), which attacks the o-difluorobenzene ring. After the intermediate transition, 2-chloro-1,3-difluorobenzene is finally formed.

In the second step, the resulting 2-chloro-1,3-difluorobenzene is reacted with a bromine source to introduce bromine atoms. The commonly used bromine source is bromine ($Br_2 $), which is also carried out under the catalysis of catalysts such as iron powder ($Fe $). Iron powder first reacts with bromine to form iron bromide ($FeBr_3 $), which catalyzes bromine to form bromine cations ($Br ^ + $). Bromine cations attack 2-chloro-1,3-difluorobenzene ring, and bromine atoms are introduced into the appropriate position through electrophilic substitution reaction to obtain 1-bromo-2-chloro-3,4-difluorobenzene.

During the reaction process, attention should be paid to the precise control of the reaction conditions. Temperature, reaction time, and the proportion of reactants all have significant effects on the process of the reaction and the purity of the product. If the halogenation reaction temperature is too high, it may cause the formation of polyhalogenated by-products; if the temperature is too low, the reaction rate will be slow and take a long time.

Furthermore, after the reaction is completed, the separation and purification of the product is also key. Methods such as distillation, extraction, column chromatography, etc. can be used to obtain high-purity 1-bromo-2-chloro-3,4-difluorobenzene.

This is only one possible synthesis method. There are various methods for organic synthesis, or other methods can be used to obtain this compound. However, it is necessary to follow the basic principles and reaction laws of organic chemistry, and to obtain satisfactory results after repeated experiments and optimization.

What are the precautions for storing and transporting 1-Bromo-2-chloro-3,4-difluorobenzene?

1-Bromo-2-chloro-3,4-difluorobenzene is an organic compound, and many things should be paid attention to during storage and transportation.

It has certain chemical activity, and when stored, the first environment is dry. The cover is exposed to water or water vapor, or causes chemical reactions such as hydrolysis, which damages the purity and quality of the material. Therefore, it needs to be stored in a dry, well-ventilated place, away from water sources and high humidity.

Temperature is also critical. High temperature environments should be avoided, which may affect the stability of the compound due to high temperature or cause reactions such as decomposition and polymerization. It should be stored in a cool place, usually 2-8 ° C. This temperature range can ensure its chemical properties are relatively stable.

Furthermore, the storage place should be away from fire sources and oxidants. This compound may be flammable, easy to burn in case of open flames and hot topics, and oxidants come into contact with it, or cause violent chemical reactions, resulting in dangerous accidents.

During transportation, the package must be strong and sealed. To prevent the package from being damaged due to vibration and collision, and the compound leaks. And the transportation vehicle should be equipped with corresponding fire protection and leakage emergency treatment equipment for emergencies.

In addition, transportation personnel should be familiar with the characteristics of the compound and emergency treatment methods. In the event of a leak, the scene should be quickly isolated, personnel should be evacuated, and irrelevant personnel should be avoided. Small leaks can be absorbed by inert materials such as sand and vermiculite; large leaks need to be constructed or excavated for containment, transferred to a special container with an explosion-proof pump, and then properly disposed of.

All these are indispensable precautions when storing and transporting 1-bromo-2-chloro-3,4-difluorobenzene, which must be strictly followed to ensure the safety of personnel and the environment.

What are the effects of 1-Bromo-2-chloro-3,4-difluorobenzene on the environment and human health?

1-Bromo-2-chloro-3,4-difluorobenzene is an organic halogen and the like. Its impact on the environment and human health cannot be ignored.

In the environment, such halogenated aromatics have considerable stability and are not easily degraded by natural forces. They may remain in soil and water for a long time. Entering the soil may affect the microbial community of the soil, causing its ecological balance to be disrupted, which in turn hinders the growth and development of plants. Entering the water body, it can accumulate in aquatic organisms through the enrichment of the food chain, affecting the normal operation of aquatic ecosystems.

As for the effects on human health, this compound can be ingested into the human body through respiratory tract, skin contact or diet. After entering the body, it may affect the human nervous system. According to previous studies, halogenated aromatics may interfere with the transmission of neurotransmitters, causing headaches, dizziness, fatigue, long-term exposure, or impairment of cognition and memory. In addition, it may also have adverse effects on the human immune system, causing immune dysfunction and susceptibility to disease. In addition, such compounds may have potential carcinogenicity. Although there is no conclusive conclusion, the risk of cancer in long-term exposure may increase, which should not be ignored. Therefore, 1-bromo-2-chloro-3,4-difluorobenzene poses a potential threat to both the environment and human health, and its production, use, and release should be strictly controlled to protect the environment and human well-being.