Chemical Formula | C7H3ClF4 |
Molecular Weight | 198.54 |
Appearance | Colorless to light yellow liquid |
Boiling Point | 128 - 130 °C |
Melting Point | N/A |
Density | 1.42 g/cm³ |
Flash Point | 33 °C |
Solubility In Water | Insoluble |
Vapor Pressure | N/A |
Refractive Index | 1.425 |
Chemical Formula | C7H3ClF4 |
Molar Mass | 198.54 g/mol |
Appearance | Colorless liquid |
Boiling Point | Around 137 - 138 °C |
Solubility In Water | Insoluble (due to non - polar nature of the aromatic ring and hydrophobic fluorine and chlorine groups) |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
Vapor Pressure | Low vapor pressure at room temperature |
Chemical Formula | C7H3ClF4 |
Molecular Weight | 198.54 |
Appearance | Colorless liquid |
Odor | Characteristic odor |
Boiling Point | 143 - 144 °C |
Density | 1.434 g/cm³ |
Solubility In Water | Insoluble |
Flash Point | 39 °C |
Refractive Index | 1.427 |
Chemical Formula | C7H3ClF4 |
Molar Mass | 198.545 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | Approximately 137 - 139 °C |
Density | Around 1.4 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
Vapor Pressure | Low vapor pressure at room temperature |
Flash Point | Around 35 - 40 °C |
What are the main uses of 2-Chloro-1-fluoro-4- (trifluoromethyl) benzene?
2-Chloro-1-fluoro-4- (trifluoromethyl) benzene, this substance has a wide range of uses. In the field of organic synthesis, it is often used as a key intermediate. Due to the characteristics of halogen atoms and trifluoromethyl atoms in its structure, it can participate in many types of chemical reactions.
In terms of substitution reactions, both chlorine atoms and fluorine atoms have certain activities and can be replaced by other functional groups. For example, in nucleophilic substitution reactions, suitable nucleophiles can attack chlorine atoms or carbon atoms attached to fluorine atoms, and then introduce new functional groups to build more complex organic compounds.
In the field of pharmaceutical research and development, such fluorine and chlorine-containing aromatic compounds often exhibit unique biological activities. Because their structures can interact with specific targets in organisms, or change the physical and chemical properties of drug molecules, such as fat solubility and stability, they may have potential value in the creation of new drugs.
In the field of materials science, 2-chloro-1-fluoro-4- (trifluoromethyl) benzene is also useful. Due to the presence of fluorine atoms, some properties of materials can be improved. For example, if fluoropolymer materials are introduced into such structural units, they may enhance the chemical resistance, thermal stability and surface properties of materials.
In addition, in pesticide synthesis, the special structure of such compounds may endow pesticides with good insecticidal, bactericidal or herbicidal activities, and the introduction of fluorine atoms may help improve the residual characteristics and biological activities of pesticides in the environment. In short, 2-chloro-1-fluoro-4 - (trifluoromethyl) benzene is an important basic raw material in many fields such as organic synthesis, medicine, materials and pesticides, and plays a key role in the development of various fields.
What are the physical properties of 2-Chloro-1-fluoro-4- (trifluoromethyl) benzene
2-Chloro-1-fluoro-4- (trifluoromethyl) benzene is a kind of organic compound. It has unique physical properties, which are described in detail by you today.
First of all, its appearance, this substance is mostly colorless to light yellow transparent liquid at room temperature. It is clear when viewed, and its flowing luster can be seen when illuminated by light. This form is easy to measure and mix in many organic synthesis reactions, which brings convenience to experimenters.
Second, its boiling point is about 135-137 ° C. The characteristics of boiling point are crucial in operations such as distillation and separation. At this temperature, 2-chloro-1-fluoro-4- (trifluoromethyl) benzene can be converted from a liquid state to a gaseous state, and then separated from other substances with different boiling points to achieve the purpose of purification.
Furthermore, its melting point is around -35 ° C. The low melting point means that the substance is stable in a liquid state at room temperature. If the temperature drops below the melting point, it will condense into a solid state.
When it comes to density, it is about 1.44g/cm ³. This density data is of great significance in the measurement of materials in chemical production and the design of storage containers. According to this, the amount of reaction materials can be accurately controlled, and the suitable storage equipment can also be reasonably selected.
Its solubility is also an important physical property. 2-Chloro-1-fluoro-4 - (trifluoromethyl) benzene is insoluble in water, but it is easily soluble in common organic solvents such as ether, acetone, dichloromethane, etc. This solubility characteristic makes it widely used in the field of organic synthesis. As a reaction solvent or a raw material involved in the reaction, it can be well miscible with many organic compounds and promote the smooth progress of the reaction.
In addition, the substance has a certain degree of volatility and will slowly evaporate into the air in an open environment. Its vapor density is heavier than that of air and is easy to accumulate at low levels. This property is crucial in the ventilation design of storage and use sites, and it is necessary to ensure good ventilation to prevent potential safety hazards caused by steam accumulation.
The physical properties of 2-chloro-1-fluoro-4 - (trifluoromethyl) benzene are of important guiding significance in the fields of organic synthesis and chemical production. They are well known and used by relevant practitioners, which can optimize the operation process, improve production efficiency and product quality.
What are the synthesis methods of 2-Chloro-1-fluoro-4- (trifluoromethyl) benzene
The synthesis method of 2-chloro-1-fluoro-4- (trifluoromethyl) benzene has many ways, and the following is selected.
First, the aromatic compound is used as the starting material and the halogenation reaction is used to form it. The benzene derivative containing the appropriate substituent can be taken first, and under specific reaction conditions, the chlorine reagent and the fluorine reagent can act in sequence. If the chlorine atom is introduced first, the commonly used chlorine reagents include chlorine gas, thionyl chloride, etc. When the catalyst such as iron powder and ferric chloride is present, the chlorination reaction can occur at a specific position of the benzene ring. Then, fluorine atoms and fluorinated reagents such as potassium fluoride are introduced to replace the groups at specific positions in suitable solvents and reaction temperatures, and finally generate the target product.
Second, the Suzuki coupling reaction strategy is adopted. First, phenylboronic acid derivatives containing halogen atoms (chlorine or fluorine) and halogenated aromatics containing trifluoromethyl groups are prepared, respectively, and then the reaction is carried out in basic conditions and suitable organic solvents under the catalysis of palladium catalysts such as tetra (triphenylphosphine) palladium. This reaction condition is relatively mild and highly selective, and can effectively construct carbon-carbon bonds to achieve the purpose of synthesizing 2-chloro-1-fluoro-4- (trifluoromethyl) benzene.
Third, the nucleophilic substitution reaction pathway can also be used. Select a suitable halogenated aromatic hydrocarbon, whose halogen atom can be replaced by a nucleophilic reagent containing fluorine and trifluoromethyl. For example, by reacting with a halogenated aromatic hydrocarbon with a nucleophilic reagent containing trifluoromethyl in the presence of a suitable solvent and base, the halogen atom can be replaced by trifluoromethyl, and then the fluorine atom can be introduced through subsequent reactions to synthesize the target compound.
There are various methods for synthesizing 2-chloro-1-fluoro-4- (trifluoromethyl) benzene, but each method has its advantages and disadvantages, which need to be selected according to the actual situation, such as raw material availability, reaction conditions, cost-effectiveness and other factors.
2-Chloro-1-fluoro-4- (trifluoromethyl) benzene during storage and transportation
2-Chloro-1-fluoro-4- (trifluoromethyl) benzene is an organic compound. When storing and transporting, care must be taken to pay attention to the following things:
First, it concerns the storage environment. This compound should be placed in a cool, dry and well-ventilated place. Because of the cool place, it can avoid the high temperature causing its volatilization to increase, or even cause dangerous chemical reactions; dry place, it can avoid moisture hydrolysis, resulting in quality damage; well-ventilated place, it can disperse harmful gases that may escape in time to ensure the safety of storage space. Do not approach fire or heat sources, because the compound may be flammable, in case of open flames and hot topics, it may explode and endanger the safety of the surroundings.
Second, the packaging must be tight. Suitable packaging materials, such as sturdy sealed containers, must be used to prevent leakage. The packaging material should be resistant to the corrosion of this compound to ensure that the packaging is intact during storage and transportation. If there is a leak in the packaging, the compound will not only cause its own loss, but also pollute the environment and endanger personal health.
Third, when transporting, you must also be extra careful. According to relevant regulations, choose a means of transportation that is in compliance. During transportation, strive to be smooth, avoid bumps and collisions, and prevent package damage. At the same time, transportation personnel must be professionally trained to be familiar with the characteristics of the compound and emergency treatment methods, and be able to properly respond in case of emergencies.
Fourth, at storage and transportation sites, warning signs are essential. Clearly label its dangerous characteristics, such as toxic, flammable, etc., to remind personnel present to be cautious, stay vigilant at all times, and strictly abide by safety procedures to prevent accidents.
All of these are the key points to pay attention to when storing and transporting 2-chloro-1-fluoro-4- (trifluoromethyl) benzene, and must not be taken lightly.
2-Chloro-1-fluoro-4- (trifluoromethyl) benzene impact on the environment and human health
2-Chloro-1-fluoro-4- (trifluoromethyl) benzene has an impact on both the environment and human health.
In terms of the environment, this substance has a certain stability and is difficult to degrade naturally. If it escapes into the atmosphere, it may be transported over a long period of time and spread to a wide area. In water and soil, it can also persist for a long time, polluting water and soil resources. It may accumulate in organisms, pass through the food chain, and amplify. For example, aquatic organisms ingest pollutants containing this substance, and then prey on higher trophic organisms, causing their concentration in organisms to gradually increase, endangering the balance of ecosystems and affecting biodiversity.
As for human health, it can enter the human body through breathing, skin contact, dietary intake, etc. To the respiratory system, or irritate the respiratory tract, cause cough, asthma, dyspnea and other diseases, long-term exposure or damage to lung function. Contact with the skin, or cause skin allergies, redness, swelling, itching, etc. If ingested orally, or damage the digestive system, cause nausea, vomiting, abdominal pain, etc. And because it contains halogen elements, or has potential carcinogenicity, teratogenicity, mutagenicity, long-term exposure, increase the risk of cancer, and threaten human reproduction and health. In short, this substance has serious harm to the environment and human health, and needs to be properly controlled to reduce its emissions and exposure.