Chemical Formula | C6ClF5 |
Molar Mass | 222.51 g/mol |
Appearance | Colorless liquid |
Boiling Point | 126 - 127 °C |
Melting Point | -23 °C |
Density | 1.65 g/cm³ |
Vapor Pressure | 3.2 kPa at 20 °C |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Flash Point | 35 °C |
Refractive Index | 1.387 |
Chemical Formula | C6ClF5 |
Molar Mass | 221.51 g/mol |
Appearance | Colorless liquid |
Boiling Point | 125 - 127 °C |
Melting Point | -35 °C |
Density | 1.698 g/cm³ (at 20 °C) |
Solubility In Water | Insoluble |
Vapor Pressure | 2.1 kPa at 25 °C |
Flash Point | 32 °C |
Refractive Index | 1.413 (at 20 °C) |
Chemical Formula | C6ClF5 |
Molecular Weight | 222.51 |
Appearance | Colorless liquid |
Odor | Characteristic odor |
Boiling Point | 125 - 126 °C |
Melting Point | -27.4 °C |
Density | 1.697 g/cm³ |
Solubility In Water | Insoluble |
Vapor Pressure | 1.33 kPa (20 °C) |
Flash Point | 32 °C |
Stability | Stable under normal conditions |
Logp | 4.54 |
What are the main uses of Chloropentafluorobenzene?
Chloropentafluorobenzene is also an organic compound. Its main uses are as follows.
In the field of organic synthesis, it is a key intermediate. Through many chemical reactions, different functional groups can be introduced to prepare organic compounds with unique structures and properties. For example, substitution reactions with nucleophiles can form novel carbon-carbon and carbon-heteroatom bonds, which are of great significance in the fields of pharmaceutical chemistry and materials science. Through such reactions, drug molecules with specific pharmacological activities or polymer materials with excellent properties can be created.
In materials science, it can be used to prepare high-performance fluoropolymers. Fluorinated polymers are widely used in aerospace, electronics and electrical appliances due to their excellent chemical stability, weather resistance and low surface energy. Chloropentafluorobenzene, as a starting material, participates in the synthesis process of polymers, giving polymers unique properties. For example, sealing materials and protective coatings used in the aerospace field can improve their chemical resistance and high temperature resistance through polymers derived from chloropentafluorobenzene, ensuring the safe operation of aircraft in complex environments.
In the electronics industry, it also has outstanding performance. It can be used to manufacture electronic chemicals, such as electronic cleaning agents, etching agents, etc. Its special chemical structure allows it to efficiently remove impurities without damaging components when cleaning the surface of electronic components. In the etching process, it can precisely control the etching rate and accuracy, and help to manufacture high-performance integrated circuits, printed circuit boards and other electronic devices, promoting the development and progress of electronic technology.
Furthermore, in the study of new catalysts, chloropentafluorobenzene is also an important research object. Through structural modification and modification, catalysts with unique catalytic activity can be prepared, which can be applied to various organic reactions, improve reaction efficiency and selectivity, and provide new ways and methods for green chemical synthesis.
What are the physical properties of Chloropentafluorobenzene?
Chloropentafluorobenzene is also an organic compound. Its physical properties are quite interesting and are described in detail as follows.
Looking at its properties, under normal circumstances, chloropentafluorobenzene is a colorless liquid, clear and clear. Although its taste is not detailed in ancient books, organic halides have a special smell, and chloropentafluorobenzene is no exception.
As for the boiling point, it is about 116-117 ° C. This temperature allows chloropentafluorobenzene to change from liquid to gaseous under normal heating conditions. The boiling point is related to its physical state under different temperature environments, and is of great significance in chemical operations, separation and purification.
In terms of melting point, it is about -35 ° C. Below this temperature, chloropentafluorobenzene will solidify into a solid state. The characteristics of the melting point determine the conditions for its storage and transportation. If the ambient temperature is too low, thermal insulation measures need to be taken to prevent it from solidifying and affecting subsequent use.
The density is about 1.61 g/cm ³, which is heavier than water. This density characteristic is crucial when it involves operations such as liquid-liquid separation. Because its density is greater than that of water, in a mixed system with water, chloropentafluorobenzene will sink to the bottom of the water, and a reasonable separation scheme can be designed accordingly.
Chloropentafluorobenzene is insoluble in water, which is hydrophobic. However, it is soluble in many organic solvents, such as ethanol, ether, etc. This solubility property makes it possible for it to be used as a solvent or a medium for reactions in organic synthesis. In an organic reaction system, selecting an appropriate organic solvent can promote the reaction, improve the reaction efficiency and yield.
Furthermore, chloropentafluorobenzene has a certain degree of volatility. Although the exact degree of volatility varies from environment to environment, it will slowly evaporate into the air at room temperature and pressure. This characteristic requires that during storage and use, attention should be paid to ventilation to prevent it from accumulating in a limited space and causing potential safety hazards.
What is the chemistry of Chloropentafluorobenzene?
Chloropentafluorobenzene is also an organic compound, and its properties are quite specific. This substance has an aromatic ring, and the chlorine atom and the pentafluoro atom on the ring coexist, which makes the chemical properties interesting.
First of all, its stability is very high due to the high electronegativity of the fluorine atom, which is connected to the benzene ring, resulting in a very stable molecular structure. The presence of fluorine atoms strengthens the carbon-fluorine bond, making chloropentafluorobenzene more difficult to react with many reagents than ordinary aromatics.
As for its reactivity, although it is stable as a whole, it can also demonstrate its activity under specific conditions. Chlorine atoms on the benzene ring can be replaced by nucleophiles. For example, in strong bases and suitable solvent environments, chlorine can be replaced by hydroxyl, amino and other nucleophilic groups. This is because the chlorine atom is affected by the electronic effect of benzene ring and fluorine atom, the electron cloud density changes, and the activity increases slightly, which is conducive to nucleophilic substitution.
And because of its fluorine content, it has a certain lipid solubility and hydrophobicity. In some organic synthesis and material applications, it can endow the product with unique physical properties. And its vapor pressure is low, its volatility is inferior to that of general small molecule aromatics, and its retention time in the environment may be slightly longer.
Furthermore, the chemical properties of chloropentafluorobenzene are affected by the reaction conditions. Temperature, pressure, and catalyst can all change the chemical reaction path and rate. Under the action of high temperature or specific catalysts, an addition reaction of benzene rings may occur, breaking the original conjugate structure and forming new derivatives.
In summary, chloropentafluorobenzene is composed of its special atoms, coexisting with stability and specific reactivity. It has potential application value in the fields of organic synthesis, materials science and other fields due to its unique chemical properties.
What is Chloropentafluorobenzene production method?
For chloropentafluorobenzene, the method of preparation has always been different. In the past, pentafluorobenzene was often used as a base to combine with chlorine-containing reagents. Capped pentafluorobenzene is active, and when it encounters chlorine-containing substances, it is formed into chloropentafluorobenzene in a suitable environment.
One method is that pentafluorobenzene reacts with a chlorinating agent, such as sulfuryl chloride, with the help of a catalyst. During the reaction, temperature, pressure, and the amount of catalyst are all key. Only by adjusting the temperature and pressure, and the catalyst is moderate, can the reaction be promoted smoothly and the yield of chloropentafluorobenzene is good. If the temperature is too high, side reactions will occur and the yield will drop; if it is too low, the reaction will be slow and time-consuming.
There are also those who use pentafluorobenzene and chlorine as raw materials. However, chlorine is very active and the reaction is difficult to control. Therefore, a suitable catalyst is often added to a specific solvent to stabilize the reaction. In this process, the properties of the solvent and the quality of the catalyst affect the direction and rate of the reaction. Good solvents can make the reactants disperse evenly and promote the homogeneity of the reaction; excellent catalysts can reduce the energy barrier of the reaction and make the reaction easy to initiate.
In addition, there are also compounds containing fluorine and chlorine that can be reacted in several steps to produce chloropentafluorobenzene. Although this process is complicated, it may have advantages in terms of easy availability of raw materials and controllable cost. Each step of the reaction needs to be carefully regulated to ensure the purity of the product and high yield.
The method of preparing chloropentafluorobenzene, or direct synthesis, or tossing and turning synthesis, all rely on precise control and suitable agents to obtain it.
Chloropentafluorobenzene what are the precautions during use
For chloropentafluorobenzene, there are many precautions to be paid attention to when using it.
It is a chemical substance with certain toxicity and danger. The first safety protection, users must wear appropriate protective equipment, such as gas masks, protective gloves and protective clothing, to prevent skin contact and inhalation. Because of its toxicity or human damage, it can have adverse effects on the respiratory tract, skin and nervous system.
Furthermore, the use of the field needs to be well ventilated. If the volatile gas of chloropentafluorobenzene accumulates, it not only increases the risk of poisoning, but also the risk of explosion. Therefore, it is crucial to ensure smooth air circulation in the working space.
Also, storage cannot be ignored. It should be stored in a cool, dry and ventilated place, away from fire sources and oxidants. Due to its chemical activity, improper storage or dangerous chemical reactions.
During use, the operation must be precise and standardized. Follow the established operating procedures and do not change the dose and use method at will. After use, properly dispose of the residue and do not dump it at will to avoid polluting the environment.
Furthermore, relevant personnel should be familiar with emergency treatment measures. In case of accidental contact or inhalation, self-rescue and mutual rescue can be carried out quickly, and medical treatment can be sought in time. In this way, the use of chloropentafluorobenzene is guaranteed to be safe and safe, and various potential dangers and hazards can be avoided.