Linshang Chemical
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2-Chloro-1,3-Dinitro-5-(Trifluoromethyl)-Benzene
Linshang Chemical
|
HS Code |
817878 |
| Chemical Formula | C7H2ClF3N2O4 |
| Molar Mass | 274.55 g/mol |
| Appearance | Solid (usually) |
| Color | May be yellow - colored solid |
| Odor | Likely has a pungent odor |
| Melting Point | Specific value would need experimental determination |
| Boiling Point | Specific value would need experimental determination |
| Density | Data dependent on experimental measurement |
| Solubility In Water | Low solubility, being an organic aromatic compound with multiple non - polar groups |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
| Flash Point | Specific value would need experimental determination |
| Hazard Class | Potentially toxic and irritant, may fall under hazardous chemicals classification |
As an accredited 2-Chloro-1,3-Dinitro-5-(Trifluoromethyl)-Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2 - chloro - 1,3 - dinitro - 5 - (trifluoromethyl) - benzene in sealed chemical - grade containers. |
| Storage | 2 - chloro - 1,3 - dinitro - 5 - (trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition sources. It should be kept in a tightly sealed container, preferably made of corrosion - resistant materials, as it is a potentially hazardous chemical. Store it separately from incompatible substances like oxidizing agents, reducing agents, and bases to prevent dangerous reactions. |
| Shipping | 2 - chloro - 1,3 - dinitro - 5 - (trifluoromethyl) - benzene is a hazardous chemical. It must be shipped in accordance with strict regulations, using appropriate packaging to prevent leakage, and labeled clearly for safe transportation. |
Competitive 2-Chloro-1,3-Dinitro-5-(Trifluoromethyl)-Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615365006308
Email: info@alchemist-chem.com
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As a leading 2-Chloro-1,3-Dinitro-5-(Trifluoromethyl)-Benzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the chemical properties of 2-chloro-1,3-dinitro-5- (trifluoromethyl) -benzene?
2-Chloro-1,3-dinitro-5- (trifluoromethyl) benzene, this is an organic compound with unique chemical properties.
Among its chemical properties, the halogen atom chlorine is active and can undergo a substitution reaction. Under the action of many nucleophiles, chlorine atoms are easily replaced. For example, in basic conditions, hydroxyl, alkoxy and other nucleophilic groups can attack the carbon atoms attached to the chlorine atom, realize chlorine substitution, and generate corresponding alcohols and ether compounds.
Two nitro groups reduce the electron cloud density of the benzene ring, causing passivation of the benzene ring, and electrophilic substitution is difficult to occur. However, nitro groups can be converted under specific reduction conditions, such as iron, hydrochloric acid, etc., and nitro groups can be reduced to amino groups to form amino-containing derivatives.
Trifluoromethyl is a strong electron-absorbing group, which affects the electron cloud distribution of benzene ring and enhances the acidity of the compound. At the same time, due to its special structure, the compound has certain chemical stability and fat solubility. It can participate in many organic synthesis reactions and has potential applications in pharmaceutical chemistry, materials science and other fields. Due to its unique chemical properties, it can be used as a synthesis intermediate to construct complex organic molecular structures.
Among its chemical properties, the halogen atom chlorine is active and can undergo a substitution reaction. Under the action of many nucleophiles, chlorine atoms are easily replaced. For example, in basic conditions, hydroxyl, alkoxy and other nucleophilic groups can attack the carbon atoms attached to the chlorine atom, realize chlorine substitution, and generate corresponding alcohols and ether compounds.
Two nitro groups reduce the electron cloud density of the benzene ring, causing passivation of the benzene ring, and electrophilic substitution is difficult to occur. However, nitro groups can be converted under specific reduction conditions, such as iron, hydrochloric acid, etc., and nitro groups can be reduced to amino groups to form amino-containing derivatives.
Trifluoromethyl is a strong electron-absorbing group, which affects the electron cloud distribution of benzene ring and enhances the acidity of the compound. At the same time, due to its special structure, the compound has certain chemical stability and fat solubility. It can participate in many organic synthesis reactions and has potential applications in pharmaceutical chemistry, materials science and other fields. Due to its unique chemical properties, it can be used as a synthesis intermediate to construct complex organic molecular structures.
What are the main uses of 2-chloro-1,3-dinitro-5- (trifluoromethyl) -benzene?
2-Chloro-1,3-dinitro-5- (trifluoromethyl) benzene is an organic compound. It has a wide range of uses and plays an important role in many fields.
In the field of organic synthesis, it is often used as a key intermediate. Because the molecule is rich in active groups such as chlorine atoms, nitro groups and trifluoromethyl groups, chlorine atoms can be successfully replaced by other functional groups through various chemical reactions, such as nucleophilic substitution reactions, to construct organic compounds with more complex and diverse structures. By ingeniously designing the reaction path, it can be used as a starting material to carefully prepare drugs, pesticides and material intermediates with specific physiological activities or functional properties.
In the field of drug research and development, its special structure may endow compounds with unique biological activities. Researchers can conduct in-depth structural modification and activity screening to explore lead compounds with potential medicinal value, and then lay the foundation for the creation of new drugs.
In the field of pesticides, the characteristics of this compound may enable it to be derived from pesticide products with high insecticidal, bactericidal or herbicidal properties. The introduction of trifluoromethyl can often significantly enhance the lipid solubility and stability of compounds, improve their sustainability and biological activity in the environment, and provide strong protection for agricultural production.
In addition, in the field of materials science, based on its structural characteristics, it can be used to synthesize polymer materials with special properties, such as materials with good thermal stability, chemical stability or optical properties, to meet the needs of different fields for special materials.
In summary, 2-chloro-1,3-dinitro-5- (trifluoromethyl) benzene has shown important application value in many important fields such as organic synthesis, drug research and development, pesticide production and materials science, providing an indispensable material basis and research starting point for the development of related industries.
In the field of organic synthesis, it is often used as a key intermediate. Because the molecule is rich in active groups such as chlorine atoms, nitro groups and trifluoromethyl groups, chlorine atoms can be successfully replaced by other functional groups through various chemical reactions, such as nucleophilic substitution reactions, to construct organic compounds with more complex and diverse structures. By ingeniously designing the reaction path, it can be used as a starting material to carefully prepare drugs, pesticides and material intermediates with specific physiological activities or functional properties.
In the field of drug research and development, its special structure may endow compounds with unique biological activities. Researchers can conduct in-depth structural modification and activity screening to explore lead compounds with potential medicinal value, and then lay the foundation for the creation of new drugs.
In the field of pesticides, the characteristics of this compound may enable it to be derived from pesticide products with high insecticidal, bactericidal or herbicidal properties. The introduction of trifluoromethyl can often significantly enhance the lipid solubility and stability of compounds, improve their sustainability and biological activity in the environment, and provide strong protection for agricultural production.
In addition, in the field of materials science, based on its structural characteristics, it can be used to synthesize polymer materials with special properties, such as materials with good thermal stability, chemical stability or optical properties, to meet the needs of different fields for special materials.
In summary, 2-chloro-1,3-dinitro-5- (trifluoromethyl) benzene has shown important application value in many important fields such as organic synthesis, drug research and development, pesticide production and materials science, providing an indispensable material basis and research starting point for the development of related industries.
What are the synthesis methods of 2-chloro-1,3-dinitro-5- (trifluoromethyl) -benzene?
The synthesis method of 2-chloro-1,3-dinitro-5- (trifluoromethyl) benzene has been known for a long time, and it has been explored and improved by many talents.
First, benzene compounds containing trifluoromethyl are used as starting materials. If a specific benzene derivative is selected, a chlorine reagent is first used to introduce chlorine atoms into the benzene ring under specific conditions. This chlorination reaction requires careful regulation of the reaction temperature, time and reagent dosage. If the temperature is too high, side reactions will easily occur, and if it is too low, the reaction will be delayed. After the chlorine atom is successfully connected, it will be nitrified. When nitrifying, choose a suitable nitrifying reagent, such as a mixed acid system, and carefully adjust its ratio to introduce nitro groups at specific positions in the benzene ring. In this process, the control of reaction conditions is particularly critical, which is related to the purity and yield of the product.
Second, other aromatic hydrocarbons are also used as starting materials to construct the structure containing trifluoromethyl, and then chlorine atoms and nitro groups are introduced in turn. For example, by using a specific reaction, aromatic hydrocarbons are reacted with reagents containing trifluoromethyl to form intermediates containing trifluoromethyl. After this intermediate is separated and purified, chlorination and nitration are carried out. Although this path is slightly complicated, the requirements for reaction conditions may vary, and it can be selected according to actual needs and raw material characteristics.
Third, there are those who use halogenated aromatics as starting materials. First, halogenated aromatics are reacted with reagents containing trifluoromethyl to introduce trifluoromethyl. This reaction requires the help of a suitable catalyst to catalyze the combination of the two. Then, a nitration reaction is carried out to introduce nitro groups at a specific position in the benzene ring. In this process, the selection and dosage of catalysts, as well as the optimization of nitration conditions, are the keys to the success or failure of the synthesis.
The above methods have their own advantages and disadvantages. In actual synthesis, the ideal synthesis path can only be obtained by carefully choosing according to factors such as raw material availability, cost considerations, and purity requirements of the target product.
First, benzene compounds containing trifluoromethyl are used as starting materials. If a specific benzene derivative is selected, a chlorine reagent is first used to introduce chlorine atoms into the benzene ring under specific conditions. This chlorination reaction requires careful regulation of the reaction temperature, time and reagent dosage. If the temperature is too high, side reactions will easily occur, and if it is too low, the reaction will be delayed. After the chlorine atom is successfully connected, it will be nitrified. When nitrifying, choose a suitable nitrifying reagent, such as a mixed acid system, and carefully adjust its ratio to introduce nitro groups at specific positions in the benzene ring. In this process, the control of reaction conditions is particularly critical, which is related to the purity and yield of the product.
Second, other aromatic hydrocarbons are also used as starting materials to construct the structure containing trifluoromethyl, and then chlorine atoms and nitro groups are introduced in turn. For example, by using a specific reaction, aromatic hydrocarbons are reacted with reagents containing trifluoromethyl to form intermediates containing trifluoromethyl. After this intermediate is separated and purified, chlorination and nitration are carried out. Although this path is slightly complicated, the requirements for reaction conditions may vary, and it can be selected according to actual needs and raw material characteristics.
Third, there are those who use halogenated aromatics as starting materials. First, halogenated aromatics are reacted with reagents containing trifluoromethyl to introduce trifluoromethyl. This reaction requires the help of a suitable catalyst to catalyze the combination of the two. Then, a nitration reaction is carried out to introduce nitro groups at a specific position in the benzene ring. In this process, the selection and dosage of catalysts, as well as the optimization of nitration conditions, are the keys to the success or failure of the synthesis.
The above methods have their own advantages and disadvantages. In actual synthesis, the ideal synthesis path can only be obtained by carefully choosing according to factors such as raw material availability, cost considerations, and purity requirements of the target product.
What are the precautions for storing and transporting 2-chloro-1,3-dinitro-5- (trifluoromethyl) -benzene?
2-Chloro-1,3-dinitro-5- (trifluoromethyl) benzene is a strong chemical, and many matters need to be carefully stored and transported.
When storing, first choose a cool and dry place. This substance is extremely sensitive to temperature and humidity, and high temperature or high humidity environment can cause its chemical properties to change, and even cause danger. The warehouse temperature should be controlled between 15 ° C and 30 ° C, and the relative humidity should not exceed 75%. Furthermore, it should be stored separately with other chemicals such as oxidizing agents, reducing agents, alkalis, etc. Because of its high chemical activity, contact with other substances can easily cause violent reactions, causing combustion and explosion. At the same time, the storage place must be well ventilated to prevent the accumulation of harmful gases.
When transporting, the packaging process is crucial. Suitable packaging materials need to be selected to ensure a tight seal to prevent leakage. Commonly used packaging is steel drums or special plastic drums. Warning labels should be clearly marked on the outside of the package to indicate its danger. The means of transportation should also be clean and dry, and no other chemicals should remain. During transportation, avoid high temperatures, open flames and strong earthquakes. Driving routes should avoid densely populated areas and important facilities, and the transportation speed should not be too fast to prevent package damage due to bumps and collisions. Escort personnel must be professionally trained, familiar with the characteristics of the substance and emergency response methods. If there is an abnormality, they can be dealt with quickly and properly.
In short, the storage and transportation of 2-chloro-1,3-dinitro-5- (trifluoromethyl) benzene is related to the overall situation of safety, and all links must be operated in strict accordance with regulations, and no slack can be made to ensure safety.
When storing, first choose a cool and dry place. This substance is extremely sensitive to temperature and humidity, and high temperature or high humidity environment can cause its chemical properties to change, and even cause danger. The warehouse temperature should be controlled between 15 ° C and 30 ° C, and the relative humidity should not exceed 75%. Furthermore, it should be stored separately with other chemicals such as oxidizing agents, reducing agents, alkalis, etc. Because of its high chemical activity, contact with other substances can easily cause violent reactions, causing combustion and explosion. At the same time, the storage place must be well ventilated to prevent the accumulation of harmful gases.
When transporting, the packaging process is crucial. Suitable packaging materials need to be selected to ensure a tight seal to prevent leakage. Commonly used packaging is steel drums or special plastic drums. Warning labels should be clearly marked on the outside of the package to indicate its danger. The means of transportation should also be clean and dry, and no other chemicals should remain. During transportation, avoid high temperatures, open flames and strong earthquakes. Driving routes should avoid densely populated areas and important facilities, and the transportation speed should not be too fast to prevent package damage due to bumps and collisions. Escort personnel must be professionally trained, familiar with the characteristics of the substance and emergency response methods. If there is an abnormality, they can be dealt with quickly and properly.
In short, the storage and transportation of 2-chloro-1,3-dinitro-5- (trifluoromethyl) benzene is related to the overall situation of safety, and all links must be operated in strict accordance with regulations, and no slack can be made to ensure safety.
What are the effects of 2-chloro-1,3-dinitro-5- (trifluoromethyl) -benzene on the environment and human health?
2-Chloro-1,3-dinitro-5- (trifluoromethyl) benzene, its impact on the environment and human health is a matter of great concern to the world.
At the environmental level, such chemicals may be quite harmful. Its chemical structure contains chlorine, nitro and trifluoromethyl groups, resulting in high chemical stability and difficult to degrade in the natural environment. If released into the soil, it may accumulate residues, gradually affecting the physical and chemical properties of the soil and the microbial community. Because soil microorganisms are quite sensitive to chemical substances, the accumulation of this substance may interfere with their normal metabolism and ecological functions, thereby affecting soil fertility and plant growth.
If it flows into the water body, it may accumulate in the sediment of the water body due to its hydrophobicity and persistence. This not only poses a threat to the living environment of aquatic organisms, but also is transmitted and amplified through the food chain. Aquatic organisms such as fish and shellfish, if exposed to such polluted water bodies for a long time, may experience stunted growth and development, decreased reproductive ability, or even death. And organisms that feed on aquatic organisms will also be affected by it, endangering the balance of the entire aquatic ecosystem.
As for human health, 2-chloro-1,3-dinitro-5 - (trifluoromethyl) benzene is also at latent risk. It can enter the human body by inhalation through the respiratory tract, or through skin contact and accidental ingestion. The nitro and halogenated groups it contains have strong electrophilicity, and may react with human biomacromolecules such as proteins and nucleic acids, causing damage to its structure and function. In the long run, it may have adverse effects on the human nervous system, immune system and many other systems. Clinical studies may show that those exposed to such substances may have neurological symptoms such as headache, dizziness, fatigue, or have low immune function, making them more susceptible to infectious diseases. In addition, due to its chemical properties, it does not rule out potential carcinogenic, teratogenic and mutagenic risks. Although relevant research may need to be in-depth, it should not be taken lightly. Overall, the potential impact of this chemical on both the environment and human health should be taken seriously and investigated in depth.
At the environmental level, such chemicals may be quite harmful. Its chemical structure contains chlorine, nitro and trifluoromethyl groups, resulting in high chemical stability and difficult to degrade in the natural environment. If released into the soil, it may accumulate residues, gradually affecting the physical and chemical properties of the soil and the microbial community. Because soil microorganisms are quite sensitive to chemical substances, the accumulation of this substance may interfere with their normal metabolism and ecological functions, thereby affecting soil fertility and plant growth.
If it flows into the water body, it may accumulate in the sediment of the water body due to its hydrophobicity and persistence. This not only poses a threat to the living environment of aquatic organisms, but also is transmitted and amplified through the food chain. Aquatic organisms such as fish and shellfish, if exposed to such polluted water bodies for a long time, may experience stunted growth and development, decreased reproductive ability, or even death. And organisms that feed on aquatic organisms will also be affected by it, endangering the balance of the entire aquatic ecosystem.
As for human health, 2-chloro-1,3-dinitro-5 - (trifluoromethyl) benzene is also at latent risk. It can enter the human body by inhalation through the respiratory tract, or through skin contact and accidental ingestion. The nitro and halogenated groups it contains have strong electrophilicity, and may react with human biomacromolecules such as proteins and nucleic acids, causing damage to its structure and function. In the long run, it may have adverse effects on the human nervous system, immune system and many other systems. Clinical studies may show that those exposed to such substances may have neurological symptoms such as headache, dizziness, fatigue, or have low immune function, making them more susceptible to infectious diseases. In addition, due to its chemical properties, it does not rule out potential carcinogenic, teratogenic and mutagenic risks. Although relevant research may need to be in-depth, it should not be taken lightly. Overall, the potential impact of this chemical on both the environment and human health should be taken seriously and investigated in depth.
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