Chemical Formula | C7H2ClF5 |
Molecular Weight | 216.536 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 145 - 147 °C |
Melting Point | N/A |
Density | 1.504 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents |
Vapor Pressure | N/A |
Flash Point | 44 °C |
Odor | Characteristic odor |
Chemical Formula | C7H2ClF5 |
Molecular Weight | 216.53 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 152 - 154 °C |
Density | 1.51 g/cm³ |
Solubility | Insoluble in water, soluble in organic solvents |
Flash Point | 45 °C |
Stability | Stable under normal conditions |
Chemical Formula | C7H2ClF5 |
Molecular Weight | 226.535 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | Around 160 - 165 °C |
Density | Approx. 1.5 - 1.6 g/cm³ |
Vapor Pressure | Low vapor pressure at room temperature |
Solubility | Insoluble in water, soluble in organic solvents like dichloromethane |
Odor | Characteristic organic odor |
Chemical Formula | C7H2ClF5 |
Molecular Weight | 216.537 |
Appearance | Liquid (assumed, typical for many similar aromatic halogenated compounds) |
Boiling Point | Estimated around 150 - 180 °C (approx. value based on similar halogenated aromatics) |
Density | Estimated around 1.5 - 1.7 g/cm³ (approx. value for halogenated aromatic compounds) |
Solubility In Water | Low solubility (aromatic and highly halogenated compounds are generally hydrophobic) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene (due to its non - polar nature) |
Vapor Pressure | Low vapor pressure at room temperature (aromatic and halogenated compounds usually have low volatility) |
What is the main use of 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene?
1-Chloro-2,3-difluoro-5- (trifluoromethyl) benzene is one of the organic compounds. Its main uses are widely used in various fields due to its special chemical structure and properties.
First, in the field of pharmaceutical chemistry, it is often a key intermediate for synthesizing drugs. Because it contains fluorine atoms, it can significantly change the physical, chemical and biological activity properties of compounds. The introduction of fluorine atoms can enhance the lipid solubility of drug molecules, making it easier to penetrate biological membranes and improve bioavailability; and can enhance the stability of molecules and prolong the metabolic cycle of drugs in the body. Therefore, pharmaceutical craftsmen often use this compound to construct drug molecular structures with specific biological activities to develop new therapeutic drugs.
Second, in the field of materials science, this compound also has important uses. It can be used as a starting material for the preparation of high-performance fluorinated materials. Fluorinated materials often have excellent chemical stability, corrosion resistance, and low surface energy due to the unique properties of fluorine atoms. Such as the preparation of fluoropolymers, which can be used to make special coatings, high-performance plastics, etc. Special coatings applied to the surface of objects can give them excellent anti-fouling, waterproof, and oil-proof properties; high-performance plastics are often used in high-end fields such as aerospace and electronics because they can withstand extreme environmental conditions.
Third, in the field of agricultural chemistry, or can be used as raw materials for the synthesis of new pesticides. Fluorinated pesticides usually have the advantages of high efficiency, low toxicity and low residue, which can effectively kill pests and weeds, and have little impact on the environment and non-target organisms. With this compound, pesticides with specific action mechanisms can be designed and synthesized to meet the needs of modern agriculture for green, environmentally friendly and efficient pesticides.
In summary, 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene, with its unique structure, plays an important role in many fields such as medicine, materials, and agriculture, providing key support for promoting technological progress and development in various fields.
What are the physical properties of 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene
1 - chloro - 2,3 - difluoro - 5 - (trifluoromethyl) benzene is an organic compound with special physical properties, which is of great significance to the fields of organic synthesis.
It is liquid at room temperature and pressure, with a certain fluidity, like smart water, and can flow freely in a specific container. Looking at its color, it is usually colorless and transparent, just like pure crystals, without variegated interference, giving people a sense of purity.
This compound has a special smell, although it is difficult to describe accurately, it has its unique smell. In a chemical experimental environment, trained personnel can use the sense of smell to distinguish it.
In terms of solubility, it is soluble in many organic solvents, such as common ether and dichloromethane. Just like salt fused into water, it can mix with these organic solvents to form a uniform mixed system. This solubility facilitates the use of reaction solvents or participation in reactions in organic synthesis, because it can make the reactants more accessible and speed up the reaction process, like building a bridge so that the reactants can meet the reaction smoothly.
The boiling point and melting point of 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene are also important physical properties. The boiling point determines the temperature conditions for its transformation from liquid to gas, and the melting point is related to the temperature of the transformation from solid to liquid. The specific value varies depending on the precise measurement conditions, but the approximate range can be obtained from the relevant chemical manuals or literature. These data are of great significance for the separation and purification of the compound in chemical production and laboratory operations. They are like precise navigators that guide the setting of operating temperature, ensure effective separation and purification, and obtain high-purity products.
Its density is also a key physical property. Compared with water, the density may be different. Through density measurement, it can be separated from other substances by methods such as liquid separation in operations such as mixture separation, according to the density. Just like cleverly using the difference in weight to screen out the desired material.
What is the chemical synthesis method of 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene
The chemical synthesis of 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene is an important topic in the field of organic synthesis. To obtain this compound, a common method can be started from a suitable aromatic compound.
First use benzene derivatives as raw materials. For example, select 2,3-difluoro-5- (trifluoromethyl) benzoic acid and convert the carboxyl group into a chlorine atom through a suitable reaction. In this process, the carboxyl group can be converted into an acid chloride first, and the commonly used reagent is sulfuryl chloride ($SOCl_2 $). When benzoic acid is heated with sulfuryl chloride, the carboxyl group can be converted into an acid chloride, and the reaction is violent and the yield is quite high. The resulting acid chloride can be reduced to chlorobenzene by treating it with an appropriate reducing agent, such as lithium aluminum hydride ($LiAlH_4 $). However, lithium aluminum hydride is a strong reducing agent and should be handled with caution because it reacts violently with water.
Halogenated aromatics can also be used as starting materials. If there is 2,3-difluoro-5- (trifluoromethyl) bromobenzene, the bromine atom can be replaced with a chlorination reagent such as lithium chloride ($LiCl $) in the presence of a suitable solvent and catalyst. Commonly used solvents such as $N, N-dimethylformamide $ ($DMF $) can effectively promote the reaction. The catalyst can be selected as cuprous iodide ($CuI $), which can accelerate the rate of halogen exchange and improve the reaction efficiency.
In addition, the strategy of gradually introducing substituents on the benzene ring is also feasible. Before introducing trifluoromethyl on the benzene ring, trifluoromethylation reagents can be used, such as sodium trifluoromethanesulfonate ($CF_3SO_2Na $), in the presence of suitable catalysts and bases. After that, fluorine atoms and chlorine atoms can be introduced in sequence. The introduction of fluorine atoms can be reacted with suitable halogenated aromatics under the action of a phase transfer catalyst, such as potassium fluoride ($KF $). The introduction of chlorine atoms can be carried out by chlorination reagents such as chlorine gas ($Cl_2 $) under the action of light or catalyst. However, there are many steps in this strategy, and the conditions of each step of the reaction need to be carefully controlled to ensure that each substituent is introduced in the expected position.
There are many methods for synthesizing 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene, each with its own advantages and disadvantages. It is necessary to carefully select the appropriate synthesis path according to the actual situation, such as the availability of raw materials, the difficulty of reaction conditions, the requirements of yield and purity.
What are the precautions for storing and transporting 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene?
1-Chloro-2,3-difluoro-5- (trifluoromethyl) benzene is an organic compound. During storage and transportation, many matters need to be paid attention to.
When storing, the first environment. When choosing a cool and ventilated warehouse, keep away from fire and heat sources. This compound is prone to danger when heated, so the temperature should be controlled at a low level, and good ventilation can avoid its accumulation.
Second, it should be stored separately from oxidants and alkalis, and should not be mixed. Because of its active chemical properties, contact with oxidants or alkalis may cause violent reactions, causing fire and explosion.
Furthermore, the warehouse should be equipped with suitable materials to contain leaks. If there is a leak, it can be collected and disposed of in time to prevent its spread from causing greater harm.
When transporting, it is necessary to ensure that the container does not leak, collapse, fall or damage. Because of its certain toxicity and corrosiveness, if the container is damaged and the material leaks, it will be unfavorable to people and the environment.
Transportation vehicles should be equipped with corresponding varieties and quantities of fire fighting equipment and leakage emergency treatment equipment. In the event of an accident on the way, they can be dealt with in time. During transportation, it is also necessary to prevent exposure to the sun, rain and high temperature. Summer transportation should be selected in the morning and evening to avoid the high temperature at noon.
When loading and unloading, it should be lightly loaded and unloaded. It is strictly forbidden to drop and hit. Because of its sensitivity to mechanical impact, rough loading and unloading can easily cause package rupture and material leakage. And pay attention to personal protection during operation, wear corresponding protective clothing, protective gloves and masks to prevent it from touching the skin and inhaling into the body.
What are the effects of 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene on the environment and human health?
1-Chloro-2,3-difluoro-5- (trifluoromethyl) benzene is one of the organic compounds. It is used in industrial synthesis, or as an intermediate, to participate in the preparation of many fine chemicals. However, this substance has an impact on the environment and human health, which cannot be ignored.
At the end of the environment, it has certain stability and is not easy to degrade. If released in nature, or in residual water and soil, menstruation will occur for many years, causing pollution to spread. Because of its hydrophobicity, it is easy to accumulate in the adipose tissue of organisms and is transmitted through the food chain. The concentration gradually rises, endangering the ecological balance and causing damage to biodiversity. Aquatic organisms such as fish, shrimp, etc., are exposed to water containing this substance, or have physiological abnormalities, hindered reproduction, and even a sharp decrease in the population.
As for personal health, exposure to this compound is also harmful. Entering the body through the respiratory tract, or irritating the mucosa of the respiratory tract, causing cough, asthma and other diseases. If exposed to the skin, it may cause allergies, redness, swelling, itching, and damage the skin barrier. Long-term exposure may increase the risk of cancer because of the halogen atoms and special groups in the structure, or cause genetic mutations that interfere with the normal metabolism and proliferation of cells. The nervous system may also be damaged, making people dizzy, weak, and difficult to concentrate, affecting life and work. Therefore, the production, use and disposal of 1-chloro-2,3-difluoro-5- (trifluoromethyl) benzene must be strictly regulated to prevent it from escaping from the environment, reduce the harm to the ecology and human body, and protect the beautiful environment and human well-being.