Chemical Formula | C8H5ClF2O |
Molar Mass | 190.574 g/mol |
Solubility In Water | Expected to be low as it's an organic compound with non - polar groups |
Solubility In Organic Solvents | Likely soluble in common organic solvents like ethanol, acetone |
Chemical Formula | C8H5ClF2O |
Molar Mass | 190.574 g/mol |
Solubility | Solubility properties would vary by solvent; likely soluble in organic solvents due to its non - polar nature |
Vapor Pressure | Low vapor pressure expected due to its relatively high molar mass and intermolecular forces |
Stability | Stable under normal conditions, but may react with strong oxidizing or reducing agents |
Reactivity | Can participate in nucleophilic substitution reactions due to the presence of the carbonyl group and the chloro - group |
What are the main uses of 2-chloro-1- (2,4-difluorophenyl) ethanone?
2-Chloro-1- (2,4-difluorophenyl) ethanone, an organic compound, has important uses in many fields.
In the process of pharmaceutical synthesis, it can be a key intermediate. In the creation process of many drugs, it is necessary to build a specific molecular structure. Taking some antibacterial drugs as an example, 2-chloro-1- (2,4-difluorophenyl) ethanone can introduce key functional groups through a series of chemical reactions, giving the drug unique antibacterial activity, so that it can effectively inhibit the growth and reproduction of pathogens.
In the field of pesticides, it is also indispensable. With its help, pesticides with high insecticidal and bactericidal properties can be synthesized. Due to its special chemical structure, it can interact with specific targets in pests or pathogens and interfere with their normal physiological activities, thus achieving the purpose of controlling pests and diseases, helping agricultural harvest, and ensuring crop yield and quality.
In addition, in the field of materials science, it may be used to synthesize special polymer materials. After polymerization with other monomers, it can endow materials with unique physical and chemical properties, such as improving the heat resistance and corrosion resistance of materials, expanding the application scenarios of materials, and playing a role in high-end fields such as aerospace and electronics.
2-chloro-1 - (2,4-difluorophenyl) ethyl ketone plays a pivotal role in the fields of medicine, pesticides and materials science, providing a key material basis for the development of various fields.
What are the physical properties of 2-chloro-1- (2,4-difluorophenyl) ethanone?
2-Chloro-1 - (2,4-difluorophenyl) ethyl ketone is also an organic compound. Its physical properties are quite elusive.
Looking at its properties, it is mostly liquid under normal conditions, but it may vary with external conditions. In terms of color, it is often a colorless to slightly yellow transparent liquid with a certain fluidity, and its luster also varies with light.
When it comes to smell, this substance emits a special smell. Although it is difficult to describe it accurately, it is slightly irritating. The smell can make people's senses alert. This smell is also one of its physical characteristics.
In terms of density, compared to water, its density may be different. In general, its density is greater than that of water, so if mixed with water, the substance will sink to the bottom of the water. This is due to its intermolecular forces and structure. In many practical applications, this property is related to the separation and mixing of substances.
Boiling point and melting point are also important physical properties. Boiling point, that is, the temperature at which a substance changes from liquid to gaseous state, 2-chloro-1- (2,4-difluorophenyl) ethyl ketone The boiling point is in a specific temperature range, which is affected by intermolecular forces such as van der Waals forces and hydrogen bonds. When the external temperature rises to the boiling point, the substance will boil and vaporize. The melting point is the temperature at which a substance changes from a solid state to a liquid state. At this temperature, the lattice structure of the substance disintegrates, the molecular motion intensifies, and the ordered solid state converts to a disordered liquid state.
The solubility cannot be ignored. In organic solvents, such as ethanol and ether, its solubility is good. Due to the principle of similarity and miscibility, the molecular structure of the substance is similar to that of organic solvent molecules and can be miscible with each other. However, in water, its solubility is poor. Due to the difference between molecular polarity and water molecular polarity, it is difficult to fully mix the two.
In addition, its refractive index is also a unique physical property. When light passes through this substance, the direction of light will change, and the refractive index is a parameter that characterizes the degree of this change. This property has important uses in the identification and purity analysis of substances.
The above physical properties are of great significance in chemical research, industrial production and related fields, and can help researchers and producers to deeply understand the characteristics of this substance, and then apply it rationally.
What is the chemical synthesis method of 2-chloro-1- (2,4-difluorophenyl) ethanone?
The chemical synthesis of 2-chloro-1- (2,4-difluorophenyl) ethyl ketone is an important topic in the field of organic synthesis. The synthesis method follows the organic chemical reaction mechanism and uses different reagents and conditions to achieve the goal.
In the past, 2,4-difluorobenzene was often used as the starting material for the synthesis of this compound. First, 2,4-difluorobenzene and acetic anhydride were catalyzed by Lewis acid such as anhydrous aluminum trichloride. In this reaction, the acyl group of acetic anhydride is acted by aluminum trichloride to form an active acyl positive ion, which attacks the benzene ring of 2,4-difluorobenzene to obtain 1 - (2,4-difluorophenyl) ethyl ketone.
Then, 1 - (2,4-difluorophenyl) ethyl ketone is chlorinated. Generally, the reaction can be initiated by light or heat in a suitable solvent such as dichloromethane with N-chlorosuccinimide (NCS) as a chlorination reagent in the presence of an initiator such as benzoyl peroxide. NCS produces a chlorine radical that attacks the carbonyl alpha-position of 1 - (2,4 - difluorophenyl) ethanone and replaces the alpha-hydrogen atom to obtain 2 - chloro - 1 - (2,4 - difluorophenyl) ethanone.
There are also those who use 2,4 - difluorobenzyl alcohol as the starting material. First, 2,4 - difluorobenzyl alcohol is oxidized to 2,4 - difluorobenzoic acid, which can be used as an oxidizing agent such as potassium permanganate. Then 2,4 - difluorobenzoic acid is converted into an acyl chloride, which is often reacted with dichlorosulfoxide. The obtained acid chloride reacts with chloromethane under the catalysis of active metal salts, and the target product 2-chloro-1- (2,4-difluorophenyl) ethyl ketone can also be obtained.
All synthesis methods have their own advantages and disadvantages, and the appropriate method must be weighed according to the actual needs and conditions to achieve the purpose of efficient, economical and environmentally friendly synthesis.
What should be paid attention to when storing and transporting 2-chloro-1- (2,4-difluorophenyl) ethanone?
2-Chloro-1- (2,4-difluorophenyl) ethyl ketone is also an organic compound. When storing and transporting, many things should be paid attention to.
First storage environment, this compound should be placed in a cool, dry and well-ventilated place. Because the shade can avoid chemical reactions caused by high temperature, drying can prevent it from deteriorating in contact with water, and good ventilation can disperse harmful gases that may accumulate. If stored in a high temperature and humid place, it may cause the compound to decompose or react with water vapor and oxygen in the environment, which will damage its quality.
Furthermore, the choice of storage container is also important. Corrosion-resistant containers are required, and the caps are corrosive to a certain extent because they contain chlorine, fluorine and other elements. Common containers such as glass materials may also be corroded and cause compound leakage if they are of poor quality or have minor cracks. Therefore, special corrosion-resistant glass containers or high-quality corrosion-resistant plastic containers are selected, and the containers must be tightly sealed to prevent volatile and external substances from invading.
As for the transportation process, it is necessary to ensure that the packaging is stable. Professional packaging materials must be used to properly wrap the compounds to prevent damage to the container due to bumps and collisions during transportation. And the transportation vehicle should be equipped with corresponding emergency treatment equipment. In case of leakage and other emergencies, it can be responded to in time. At the same time, transport personnel should be familiar with the characteristics of the compound and emergency treatment methods, so as to ensure safety during transportation and avoid accidents. In short, the storage and transportation of 2-chloro-1 - (2,4-difluorophenyl) ethyl ketone requires careful treatment of various factors such as the environment, containers, packaging and personnel to ensure its safety and quality.
What are the effects of 2-chloro-1- (2,4-difluorophenyl) ethanone on the environment and human health?
2-Chloro-1 - (2,4-difluorophenyl) ethyl ketone, this is an organic compound. Its impact on the environment and human health cannot be ignored.
At the environmental end, it may have many effects. If it is released into the soil, or interacts with various substances in the soil, it changes the chemical properties of the soil, causing soil fertility or being affected. For example, it may interfere with the normal metabolism and reproduction of microorganisms in the soil. Microorganisms are crucial in the soil ecosystem and participate in key processes such as organic matter decomposition and nutrient cycling. If their activities are disturbed, the soil ecological balance may be broken. And if it seeps into groundwater, or causes groundwater pollution, threatening water safety, and many areas rely on groundwater as a drinking water source, this compound may remain in the water, difficult to degrade, affect water quality, and make the water body unsuitable for drinking and other living purposes.
If dispersed into the atmosphere, it may participate in photochemical reactions. Because it contains chlorine, fluorine and other elements, or interacts with other pollutants in the atmosphere such as nitrogen oxides, hydrocarbons, etc., under light conditions, secondary pollutants such as ozone are generated, which exacerbates the degree of air pollution, affects air quality, and causes adverse effects on the surrounding ecological environment and climate.
As for human health, there is also a potential threat. Inhaled through the respiratory tract, this compound may irritate the respiratory mucosa, causing uncomfortable symptoms such as cough and asthma. Long-term exposure may increase the risk of respiratory diseases, such as chronic obstructive pulmonary disease. If it enters the human body through skin contact or penetrates the skin barrier, it will interfere with the normal physiological functions of the human body. Some organic halides are fat-soluble, easy to accumulate in human adipose tissue, long-term accumulation or damage important organ functions such as liver and kidney, and affect human metabolism and detoxification. And studies suggest that such halogenated organic compounds may have certain teratogenic and carcinogenic potential. Although more research is needed to support the relevant definitive evidence, the latent risk should not be underestimated. Therefore, for 2-chloro-1- (2,4-difluorophenyl) ethyl ketone, the production, use and discharge process should be strictly controlled to reduce its adverse effects on the environment and human health.