Chemical Formula | C6H4ClF |
Molar Mass | 128.546 g/mol |
Appearance | Colorless liquid |
Odor | Aromatic odor |
Density | 1.228 g/cm³ at 20 °C |
Boiling Point | 117 - 118 °C |
Melting Point | -35 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in many organic solvents |
Vapor Pressure | 1.6 kPa at 20 °C |
Flash Point | 15 °C |
Chemical Formula | C6H4ClF |
Molar Mass | 116.546 g/mol |
Appearance | Colorless liquid |
Odor | Aromatic odor |
Density | 1.22 g/cm³ |
Boiling Point | 115 - 117 °C |
Melting Point | -45 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in many organic solvents |
Flash Point | 15 °C |
Vapor Pressure | 2.35 kPa at 25 °C |
Chemical Formula | C6H4ClF |
Molar Mass | 116.546 g/mol |
Appearance | Colorless liquid |
Odor | Pungent, aromatic odor |
Density | 1.197 g/cm³ at 20 °C |
Boiling Point | 116 - 118 °C |
Melting Point | -48 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Flash Point | 19 °C |
Vapor Pressure | 4.3 hPa at 20 °C |
Refractive Index | 1.505 at 20 °C |
What are the main uses of 4-CHLOROFLUOROBENZENE?
4-Chlorofluorobenzene, which is a colorless and transparent liquid with a special odor. This substance has a wide range of uses in the chemical industry, and today I will describe its main uses in detail.
The first to bear the brunt is as an intermediary in organic synthesis. In the process of pharmaceutical synthesis, it can be turned into a key pharmaceutical intermediate through many reactions. For example, to synthesize specific antibacterial drugs, 4-chlorofluorobenzene can introduce specific functional groups by substitution, condensation and other reactions to build the basic structure of drug molecules, paving the way for the synthesis of drugs with high antibacterial activity.
Furthermore, it also plays an important role in the field of pesticides. It can be used as an important raw material for the synthesis of pesticides. Through a series of chemical reactions, high-efficiency pesticides, fungicides and other pesticide varieties are obtained. Its unique chemical structure can endow pesticides with excellent biological activity and environmental compatibility, help agricultural pest control, and ensure crop harvest.
In addition, 4-chlorofluorobenzene also plays a role in the field of materials science. In the synthesis of new polymer materials, it can participate in polymerization reactions and become a part of the polymer structure. In order to improve the properties of materials, such as enhancing the heat resistance and chemical corrosion resistance of materials, so that materials can be used in high-end fields such as aerospace and electronics.
In summary, 4-chlorofluorobenzene is widely used and plays a pivotal role in the chemical industry. With the advance of science and technology, its application prospects will also be broader.
What are the physical properties of 4-CHLOROFLUOROBENZENE?
4-Chlorofluorobenzene is also an organic compound. It has unique physical properties, let me tell you one by one.
Looking at its properties, under room temperature and pressure, 4-chlorofluorobenzene is a colorless and transparent liquid, just like a clear spring, pure and clear. The appearance characteristics of this liquid lay an intuitive foundation for its application in many scenarios.
Smell its smell, 4-chlorofluorobenzene emits a special fragrance. Although its fragrance is not as elegant as the orchid, it is also unique. This special smell can be used as an important marker for identifying the substance, which is quite crucial in practical identification operations.
When it comes to boiling point, the boiling point of 4-chlorofluorobenzene is between 116 ° C and 117 ° C. When the temperature rises to this range, the substance is like a butterfly of feather, transforming from liquid light to gaseous state. This boiling point characteristic plays a crucial role in chemical operations such as distillation and separation.
As for the melting point, it is about -56.5 ° C. When the ambient temperature drops, 4-chlorofluorobenzene is like quiet ice, solidifying from a flowing state to a solid state. This melting point property is crucial for the control of material storage and transportation conditions.
Once again, the density of 4-chlorofluorobenzene is about 1.225g/cm ³, which is heavier than water. Just like a stone entering water, this density characteristic is of great significance in the actual process of liquid-liquid separation and mixing.
In terms of solubility, 4-chlorofluorobenzene is slightly soluble in water, just like water droplets on a lotus leaf, and it is difficult to dissolve with water. However, it is easily soluble in organic solvents, such as ethanol, ether, acetone, etc., just like salt entering water. This solubility property is widely used in organic synthesis, extraction and other fields.
In addition, the vapor pressure of 4-chlorofluorobenzene has a specific value at a specific temperature, and its vapor relative density is also different from that of air. These two factors are key considerations in the ventilation and gas diffusion of chemical production.
To sum up, the various physical properties of 4-chlorofluorobenzene are intertwined to build their unique material properties, which are of great value in many fields such as chemical industry, medicine, and materials.
What is the chemistry of 4-CHLOROFLUOROBENZENE?
4-Chlorofluorobenzene is also an organic compound. It has the commonality of halogenated aromatic hydrocarbons. On the benzene ring, chlorine and fluorodihalogen atoms coexist, resulting in its unique chemical properties.
The chemical activity of this substance varies significantly due to the electronegativity of halogen atoms. Fluorine atoms are extremely electronegative, and above the benzene ring, they have a great impact on the distribution of electron clouds, resulting in a decrease in the electron cloud density of the benzene ring. Although chlorine atoms are slightly inferior to fluorine, they also have electron-withdrawing effects. The synergy of the two makes the electrophilic substitution activity of benzene ring lower than that of benzene.
In the electrophilic substitution reaction, the reaction check point and rate of 4-chlorofluorobenzene are Fluorine and chlorine are both ortho and para-sites, but fluorine has a stronger positioning effect, so electrophilic reagents tend to attack the ortho and para-sites of the benzene ring. However, due to the combined effect of steric hindrance and electronic effect, the actual proportion of reaction products is complex and variable.
Furthermore, the halogen atom of 4-chlorofluorobenzene can participate in many reactions. Chlorine atoms can undergo nucleophilic substitution. Under suitable nucleophilic reagents and reaction conditions, chlorine atoms can be replaced by other groups, which is an important way to introduce new functional groups in organic synthesis. Although fluorine atoms have slightly lower nucleophilic substitution activity, they can also participate in the reaction under specific conditions, and because of the high carbon-fluorine bond energy formed, the product has unique stability and chemical properties. 4-Chlorofluorobenzene is widely used in the field of organic synthesis and is often a key intermediate for the preparation of drugs, pesticides and functional materials. Due to its unique chemical properties, complex and diverse organic molecular structures can be constructed through a variety of organic reactions to meet the needs of different fields.
What is 4-CHLOROFLUOROBENZENE production method?
4-Chlorofluorobenzene is also an organic compound. The methods for its preparation are as follows.
First, fluorobenzene is used as the starting material to react with chlorinated reagents. Under suitable reaction conditions, such as with the help of catalysts, when the temperature and pressure are appropriate, chlorinated reagents can introduce chlorine atoms into the benzene ring of fluorobenzene. Commonly used chlorinated reagents include chlorine gas, thionyl chloride, etc. Taking chlorine gas as an example, this reaction often needs to be under light or under the condition of an initiator to occur smoothly. Light can cause chlorine molecules to homogenize, generating chlorine free radicals, which attack the fluorobenzene ring, and through a series of fundamental reactions, the final result is 4-chlorofluorobenzene. In this process, temperature control is very important. If it is too high, side reactions will occur and the yield will decrease; if it is too low, the reaction will be slow and take a long time.
Second, 4-chloroaniline can also be used as a raw material. First, 4-chloroaniline is denitrified, and sodium nitrite and hydrochloric acid are used as reagents. In a low temperature environment, 4-chloroaniline can be converted into diazonium salts. Subsequently, fluoroboronic acid is used as a fluorine source, and the diazonium salt reacts with it to form 4-chlorophenylfluoroboronic acid diazonium salt. This salt is decomposed by heat, releasing nitrogen gas, and generating 4-chlorofluorobenzene at the same time. This pathway step is slightly complicated, but the selectivity is quite good,
Third, take p-dichlorobenzene as the starting material and react with fluorinating reagents. Fluorinating reagents such as potassium fluoride can replace one of the chlorine atoms of p-dichlorobenzene in the presence of appropriate solvents and catalysts to generate 4-chlorofluorobenzene. This reaction requires attention to the choice of solvent. Polar aprotic solvents can often promote the reaction, because it can dissolve potassium fluoride and is beneficial to the stability of reaction intermediates. At the same time, the catalyst can reduce the activation energy of the reaction and improve the reaction rate and yield.
The methods for preparing 4-chlorofluorobenzene have their own advantages and disadvantages. In actual production, it needs to be selected according to the availability of raw materials, cost, yield, purity and other factors.
4-CHLOROFLUOROBENZENE what are the precautions during use
4-Chlorofluorobenzene is also a chemical substance. In the process of its use, all things that should be paid attention to should not be ignored.
First of all, its properties should be made clear. 4-Chlorofluorobenzene is toxic and can be harmful when touched, smelled or entered into the body. When operating, take care of suitable protective gear, such as gloves, masks, goggles, to prevent it from connecting with the body, and to prevent it from entering the lungs.
times, this substance is flammable. When stored and used, it must be kept away from fire sources, heat and oxidants. Store in a cool, well-ventilated place and seal it to prevent it from dissipating in the air, increasing the risk of combustion and explosion.
Also, in the place where 4-chlorofluorobenzene is used, ventilation must be improved. Set up an effective ventilation system to make the air smooth, reduce its gas concentration, and avoid accumulation and risk.
Furthermore, if 4-chlorofluorobenzene accidentally touches the body or enters the eye during use, flush it with water quickly, and seek medical attention as soon as possible. If you take it by mistake, you should not be lazy, ask for medical help quickly, and do not give medicine indiscriminately.
Repeat, dispose of 4-chlorofluorobenzene waste, according to regulations. Do not discard it indiscriminately, and must be collected and dealt with in a proper way to avoid pollution and harm all living beings.
In short, when using 4-chlorofluorobenzene, be careful, pay attention to all aspects, and follow the rules to ensure safety and avoid disasters.