Chemical Formula | C8H5ClF2O |
Molar Mass | 190.574 g/mol |
Chemical Formula | C8H5ClF2O |
Molar Mass | 190.574 g/mol |
Appearance | A colorless to light yellow liquid |
Boiling Point | Approximately 220 - 225 °C |
Solubility In Water | Low solubility, being an organic compound |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, ethyl acetate |
Vapor Pressure | Low vapor pressure, being a relatively high - boiling liquid |
Chemical Formula | C8H5ClF2O |
Molecular Weight | 190.574 |
Chemical Formula | C8H5ClF2O |
Molar Mass | 190.574 g/mol |
Appearance | Solid (presumably, based on typical nature of such compounds) |
Solubility In Water | Likely low solubility, as it is an organic compound with non - polar groups |
Solubility In Organic Solvents | Expected to be soluble in common organic solvents like dichloromethane, chloroform, etc. |
What are the main uses of 2-Chloro-1- (3,4-difluorophenyl) ethanone?
2-Chloro-1- (3,4-difluorophenyl) ethyl ketone is also a compound commonly used in organic synthesis. It has a wide range of uses and has important applications in medicine, pesticides and other fields.
In the field of medicine, this compound is often a key intermediate. Because its molecular structure contains specific functional groups, it can undergo various chemical reactions to construct complex structures with biological activity. If it is used as a starting material, it can be used for nucleophilic substitution, condensation and other reactions to synthesize a variety of pharmacologically active compounds, or as potential drug molecules, or can be used to improve the properties of existing drugs, improve efficacy and reduce side effects.
In the field of pesticides, 2-chloro-1 - (3,4-difluorophenyl) ethyl ketone also plays an important role. It can be chemically converted to synthesize pesticide ingredients with high insecticidal, bactericidal or herbicidal activities. Due to its unique structure, the derived pesticides may have high selectivity, low toxicity, and environmental friendliness, which is in line with the development trend of modern pesticides.
In addition, in the fields of materials science, this compound may also have potential uses. Its special structure may endow materials with specific properties, such as improving material stability, solubility, etc. In conclusion, 2-chloro-1- (3,4-difluorophenyl) ethyl ketone, with its unique molecular structure, has shown important value in many fields and is one of the key objects of organic synthetic chemistry research.
What are the physical properties of 2-Chloro-1- (3,4-difluorophenyl) ethanone?
2-Chloro-1- (3,4-difluorophenyl) ethyl ketone, this is an organic compound. According to its physical properties, under normal temperature and pressure, it is mostly in a liquid state. Due to its molecular structure containing specific functional groups, it has a certain polarity, so it shows good solubility in organic solvents, such as common ethanol, ether, dichloromethane, etc. It can dissolve with it.
Its boiling point is also a specific value, about a certain range (the specific value is subject to experimental determination). This property is quite useful when separating and purifying. And the color state of this substance is usually a colorless to light yellow transparent liquid, under light or with a unique luster.
Furthermore, its density is also a specific parameter, which may be different from that of water. In practical operation and application, this is an important consideration. As for the smell, or the special taste, although it is difficult to describe accurately, its unique smell can be used as one of the identification aids. In addition, its melting point is also a fixed value (requiring accurate experimental determination), which is crucial in the study of the phase transition of substances.
The above physical properties are key basic information in many fields such as organic synthesis and drug development, and whether they can be applied to specific reactions and processes.
What are the synthesis methods of 2-Chloro-1- (3,4-difluorophenyl) ethanone?
The synthesis method of 2-chloro-1 - (3,4-difluorophenyl) ethyl ketone has been studied by chemists throughout the ages, and there are many paths.
First, 3,4-difluoroacetophenone is used as the starting material and is prepared by halogenation reaction. Among them, the halogenating reagent can be chlorine or sulfoxide chloride. If chlorine is used, at a suitable temperature and in the presence of a catalyst, the chlorine gas reacts with 3,4-difluoroacetophenone, and the chlorine atom replaces the alpha-hydrogen atom to obtain the target product. For example, 3,4-difluoroacetophenone is placed in a reactor, chlorine gas is introduced, and the reaction is initiated by appropriate light or initiator. The temperature is controlled for several times. After separation and purification, 2-chloro-1 - (3,4-difluorophenyl) ethanone can be obtained.
Second, start from 3,4-difluorobenzoic acid. First, 3,4-difluorobenzoic acid is converted into acyl chloride, and common chlorination reagents such as dichlorosulfoxide can react to obtain 3,4-difluorobenzoyl chloride. After that, Grignard reagent is used to react with it, such as methyl Grignard reagent prepared by chloromethane, and then reacted with 3,4-difluorobenzoyl chloride. After hydrolysis and other steps, chloromethyl can be introduced to obtain the target compound. This process requires strict anhydrous and anaerobic conditions to ensure the smooth reaction.
Third, through the Fu-gram acylation reaction of aromatics. Using 3,4-difluorobenzene and chloroacetyl chloride as raw materials, under the action of Lewis acid catalysts such as aluminum trichloride, the Fu-gram acylation reaction occurs. Mix 3,4-difluorobenzene with chloroacetyl chloride in a certain proportion, add aluminum trichloride, and react at a suitable temperature. After subsequent treatment, such as washing, liquid separation, distillation, etc., pure 2-chloro-1 - (3,4-difluorophenyl) ethyl ketone can be obtained.
All synthesis methods have their own advantages and disadvantages, and they need to be selected according to the actual situation, such as the availability of raw materials, the ease of control of reaction conditions, and the purity requirements of the product.
What to pay attention to when storing and transporting 2-Chloro-1- (3,4-difluorophenyl) ethanone
2-Chloro-1- (3,4-difluorophenyl) ethyl ketone is also an organic compound. During storage and transportation, many matters need to be paid attention to.
Bear the brunt, and the storage environment is crucial. This compound should be stored in a cool, dry and well-ventilated place. If placed in a high temperature environment, it may change its chemical properties due to rising temperature, or cause adverse reactions such as decomposition and polymerization, which will damage its quality. If the environment is humid, moisture may react with the compound, affecting its purity and stability. And poor ventilation, once the compound evaporates, it will accumulate in a limited space, or increase the risk of fire and explosion.
Furthermore, the packaging must be solid and reliable. Appropriate packaging materials should be selected to ensure that they can effectively block external factors. Packaging should be able to withstand a certain amount of pressure and vibration, and will not be damaged and leaked during transportation. If the packaging is improper, the compound will leak, which will not only pollute the environment, but also pose a serious threat to personnel safety.
When transporting, relevant regulations and operating procedures must be strictly followed. Transportation vehicles should be equipped with necessary emergency treatment equipment and protective equipment to prevent accidents. Drivers and escorts should be familiar with the characteristics of the compound and emergency treatment methods, and can respond quickly and correctly in case of emergencies.
In addition, this compound may be toxic and corrosive, and obvious warning signs should be set up at storage and transportation sites to remind personnel to pay attention to safety. Those exposed to the compound must take appropriate protective measures, such as wearing protective gloves, masks, goggles, etc., to avoid direct contact and inhalation to prevent damage to the body.
What are the effects of 2-Chloro-1- (3,4-difluorophenyl) ethanone on the environment and human health?
2-Chloro-1- (3,4-difluorophenyl) ethyl ketone, this is an organic compound. The impact on the environment and human health, let me tell you in detail.
First talk about the impact on the environment. After entering the natural environment, it is difficult to degrade due to its special chemical structure. If released in water bodies, it will cause many hazards to aquatic organisms. Long-term exposure to water bodies containing this substance may cause physiological disorders. For example, the gill tissue of fish may be damaged, which affects its respiratory function; its reproductive system may also be disturbed, which may reduce the reproductive capacity of fish and reduce the population. In soil, it will change the structure and function of soil microbial community. Soil microorganisms are essential to soil fertility and material circulation. The existence of these substances may inhibit the growth of beneficial microorganisms, causing imbalance in the soil ecosystem and affecting plant growth.
Let's talk about the impact on human health. It is irritating. If it comes into contact with human skin, it may cause contact dermatitis, erythema, itching, blisters and other symptoms. When the eyes come into contact with it, the irritation is more intense, or it may cause eye pain, redness and swelling, and in severe cases damage vision. If inhaled inadvertently, it will irritate the respiratory tract, causing symptoms such as cough, asthma, and breathing difficulties. Long-term inhalation may cause chronic damage to the lungs, increasing the risk of respiratory diseases. In more serious cases, this substance may be potentially carcinogenic. Although there is no conclusive evidence of carcinogenesis in humans, relevant animal experiments have shown that long-term exposure to this substance increases the risk of cancer in experimental animals.
Therefore, when producing and using 2-chloro-1- (3,4-difluorophenyl) ethyl ketone, it is necessary to take proper protective measures and environmental management measures to reduce its harm to the environment and human health.