Linshang Chemical
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2,4-Dichloro-1-Methyl-3-Nitro-5-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
265453 |
| Chemical Formula | C8H4Cl2F3NO2 |
| Molecular Weight | 274.02 |
| Appearance | Solid (likely, based on similar compounds) |
| Physical State At Room Temperature | Solid |
| Solubility In Water | Low (due to non - polar nature of the molecule) |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
| Vapor Pressure | Low (due to its solid state and relatively high molecular weight) |
As an accredited 2,4-Dichloro-1-Methyl-3-Nitro-5-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle of 2,4 - dichloro - 1 - methyl - 3 - nitro - 5 - (trifluoromethyl)benzene. |
| Storage | 2,4 - dichloro - 1 - methyl - 3 - nitro - 5 - (trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, ignition sources, and oxidizing agents. Store in a tightly - sealed container, preferably made of corrosion - resistant materials, to prevent leakage and contamination. |
| Shipping | 2,4 - dichloro - 1 - methyl - 3 - nitro - 5 - (trifluoromethyl)benzene is shipped in specialized containers. Compliance with strict chemical shipping regulations is ensured, including proper labeling, packaging to prevent leaks, and transport via approved carriers. |
Competitive 2,4-Dichloro-1-Methyl-3-Nitro-5-(Trifluoromethyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 2,4-Dichloro-1-Methyl-3-Nitro-5-(Trifluoromethyl)Benzene in China?
As a trusted 2,4-Dichloro-1-Methyl-3-Nitro-5-(Trifluoromethyl)Benzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
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Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
As a leading 2,4-Dichloro-1-Methyl-3-Nitro-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 main uses of 2,4-dichloro-1-methyl-3-nitro-5- (trifluoromethyl) benzene?
2% 2C4-dihydro-1-methyl-3-furanyl-5 - (trifluoromethyl) benzene has a wide range of main uses. In the field of medicine, this compound is often a key raw material for the creation of new drugs. Due to its unique chemical structure, it can precisely bind to specific biological targets in the human body, or regulate physiological functions, or fight disease invasions. For example, in the development of anti-inflammatory drugs, its structural properties can be used to design drugs that can effectively inhibit the release of inflammatory factors, relieve inflammatory symptoms, and relieve patient pain.
In the field of pesticides, this substance also plays an important role. With its ability to interfere with the unique physiological mechanisms of certain pests, it can be made into highly effective insecticides. It can accurately act on the nervous system or respiratory system of pests, causing physiological dysfunction of pests, achieving the purpose of killing pests, and has a relatively small impact on the environment, which can meet the needs of modern agriculture for green and environmentally friendly pesticides.
In the field of materials science, 2% 2C4-dihydro-1-methyl-3-furanyl-5 - (trifluoromethyl) benzene can be used as a functional additive. Adding polymer materials can significantly improve material properties, such as enhancing material resistance to chemical corrosion and improving thermal stability. The materials optimized by this can be widely used in high-end fields such as aerospace and electronic equipment to meet their strict performance requirements.
In summary, 2% 2C4-dihydro-1-methyl-3-furyl-5- (trifluoromethyl) benzene plays an important role in many fields such as medicine, pesticides and materials science, and has broad application prospects and important research value.
In the field of pesticides, this substance also plays an important role. With its ability to interfere with the unique physiological mechanisms of certain pests, it can be made into highly effective insecticides. It can accurately act on the nervous system or respiratory system of pests, causing physiological dysfunction of pests, achieving the purpose of killing pests, and has a relatively small impact on the environment, which can meet the needs of modern agriculture for green and environmentally friendly pesticides.
In the field of materials science, 2% 2C4-dihydro-1-methyl-3-furanyl-5 - (trifluoromethyl) benzene can be used as a functional additive. Adding polymer materials can significantly improve material properties, such as enhancing material resistance to chemical corrosion and improving thermal stability. The materials optimized by this can be widely used in high-end fields such as aerospace and electronic equipment to meet their strict performance requirements.
In summary, 2% 2C4-dihydro-1-methyl-3-furyl-5- (trifluoromethyl) benzene plays an important role in many fields such as medicine, pesticides and materials science, and has broad application prospects and important research value.
What are the physical properties of 2,4-dichloro-1-methyl-3-nitro-5- (trifluoromethyl) benzene?
2% 2C4-difluoro-1-methyl-3-chloro-5- (trifluoromethyl) benzene, which is one of the organic compounds. Its physical properties are unique, and this is for you to describe in detail.
The appearance of the first word, at room temperature, is mostly a colorless to light yellow transparent liquid, clear and free of impurities. Viewed under light, it can be seen that its flow is agile, like the brilliance of pearl jade.
As for the smell, it has a special aromatic smell, but it is not rich and pungent. A little smell makes it feel slightly fresh, but it is different from the ordinary floral and fruity aroma, with a unique chemical charm. The boiling point of
is very critical, about a certain temperature range, this characteristic is very important in chemical operations such as separation and purification. The value of the boiling point makes it possible to vaporize and separate from the mixed system under a specific temperature environment, so as to achieve the purpose of purification. The melting point of
also cannot be ignored. At a specific low temperature, the substance will gradually change from liquid to solid state, and this transition temperature is the melting point. The exact value of the melting point is related to its physical form under different temperature conditions, which is of great significance for the setting of storage and transportation conditions.
In terms of solubility, it exhibits good solubility in some organic solvents. For example, when mixed with some common organic solvents, it can be rapidly miscible and form a uniform and stable solution. In organic synthesis reactions, this property is often used to dissolve reactants to promote the smooth progress of the reaction, acting as a bridge, so that the reactants can be fully contacted and accelerate the reaction process.
Density is also an important physical property. The specific value of the relative density indicates the quality difference of the substance per unit volume compared with common substances such as water. This property is a key consideration in the operation of material measurement and stratification separation in chemical production, which helps to accurately control the production process. The physical properties of 2% 2C4-difluoro-1-methyl-3-chloro-5- (trifluoromethyl) benzene are of great significance in many fields such as chemical industry and materials, and have a profound impact on its practical application and operation process.
The appearance of the first word, at room temperature, is mostly a colorless to light yellow transparent liquid, clear and free of impurities. Viewed under light, it can be seen that its flow is agile, like the brilliance of pearl jade.
As for the smell, it has a special aromatic smell, but it is not rich and pungent. A little smell makes it feel slightly fresh, but it is different from the ordinary floral and fruity aroma, with a unique chemical charm. The boiling point of
is very critical, about a certain temperature range, this characteristic is very important in chemical operations such as separation and purification. The value of the boiling point makes it possible to vaporize and separate from the mixed system under a specific temperature environment, so as to achieve the purpose of purification. The melting point of
also cannot be ignored. At a specific low temperature, the substance will gradually change from liquid to solid state, and this transition temperature is the melting point. The exact value of the melting point is related to its physical form under different temperature conditions, which is of great significance for the setting of storage and transportation conditions.
In terms of solubility, it exhibits good solubility in some organic solvents. For example, when mixed with some common organic solvents, it can be rapidly miscible and form a uniform and stable solution. In organic synthesis reactions, this property is often used to dissolve reactants to promote the smooth progress of the reaction, acting as a bridge, so that the reactants can be fully contacted and accelerate the reaction process.
Density is also an important physical property. The specific value of the relative density indicates the quality difference of the substance per unit volume compared with common substances such as water. This property is a key consideration in the operation of material measurement and stratification separation in chemical production, which helps to accurately control the production process. The physical properties of 2% 2C4-difluoro-1-methyl-3-chloro-5- (trifluoromethyl) benzene are of great significance in many fields such as chemical industry and materials, and have a profound impact on its practical application and operation process.
What are the chemical properties of 2,4-dichloro-1-methyl-3-nitro-5- (trifluoromethyl) benzene?
2% 2C4-difluoro-1-methyl-3-chloro-5- (trifluoromethyl) benzene has unique and interesting chemical properties. This compound contains halogen elements such as fluorine and chlorine. The fluorine atom has strong electronegativity, which can significantly affect the distribution of molecular electron clouds, resulting in high stability and unique reactivity.
In terms of physical properties, due to the large number of fluorine atoms, the intermolecular force may be different from that of conventional aromatics, and the properties such as melting point and solubility will change. The electronegativity of fluorine atoms makes the molecule have a certain polarity, and its solubility in polar solvents may be better than that of non-polar aromatics.
Discussing the chemical properties, first, the common nucleophilic substitution reaction of halogenated aromatics may have unique performance in this compound. Chlorine atoms as leaving groups can undergo nucleophilic substitution under suitable nucleophilic reagents and reaction conditions. However, due to the influence of ortho-fluorine atoms, the reactivity is different from that of ordinary chloroaromatic hydrocarbons. Electron-absorbing action of fluorine atoms may make chlorine atoms more likely to leave, but steric hindrance may also produce inhibitory effects.
Second, due to the presence of multiple fluorine atoms, this compound has unique performance in some reactions involving fluorine chemistry. For example, in the electrofluorination reaction, due to the presence of fluorine atoms in the molecule, its regioselectivity and reactivity are affected. And in the redox reaction, the stabilization of fluorine atoms can change the difficulty of molecular oxidation state change.
Third, the density of aromatic ring electron clouds is affected by substituents. The density distribution of aromatic ring electron clouds changes under the combined action of methyl donators, fluorine, chlorine and trifluoromethyl, which in turn affects the activity and regioselectivity of aromatic ring electrophilic substitution reactions. Overall, the chemical properties of 2% 2C4-difluoro-1-methyl-3-chloro-5 - (trifluoromethyl) benzene are complex and unique due to the synergy of various substituents, and may have important application value in organic synthesis, materials science and other fields.
In terms of physical properties, due to the large number of fluorine atoms, the intermolecular force may be different from that of conventional aromatics, and the properties such as melting point and solubility will change. The electronegativity of fluorine atoms makes the molecule have a certain polarity, and its solubility in polar solvents may be better than that of non-polar aromatics.
Discussing the chemical properties, first, the common nucleophilic substitution reaction of halogenated aromatics may have unique performance in this compound. Chlorine atoms as leaving groups can undergo nucleophilic substitution under suitable nucleophilic reagents and reaction conditions. However, due to the influence of ortho-fluorine atoms, the reactivity is different from that of ordinary chloroaromatic hydrocarbons. Electron-absorbing action of fluorine atoms may make chlorine atoms more likely to leave, but steric hindrance may also produce inhibitory effects.
Second, due to the presence of multiple fluorine atoms, this compound has unique performance in some reactions involving fluorine chemistry. For example, in the electrofluorination reaction, due to the presence of fluorine atoms in the molecule, its regioselectivity and reactivity are affected. And in the redox reaction, the stabilization of fluorine atoms can change the difficulty of molecular oxidation state change.
Third, the density of aromatic ring electron clouds is affected by substituents. The density distribution of aromatic ring electron clouds changes under the combined action of methyl donators, fluorine, chlorine and trifluoromethyl, which in turn affects the activity and regioselectivity of aromatic ring electrophilic substitution reactions. Overall, the chemical properties of 2% 2C4-difluoro-1-methyl-3-chloro-5 - (trifluoromethyl) benzene are complex and unique due to the synergy of various substituents, and may have important application value in organic synthesis, materials science and other fields.
What are the synthesis methods of 2,4-dichloro-1-methyl-3-nitro-5- (trifluoromethyl) benzene?
To prepare 2,4-difluoro-1-methyl-3-chloro-5- (trifluoromethyl) benzene, there are many methods. The main ones are selected and described below.
First, it can be prepared from halogenated aromatics by nucleophilic substitution reaction. First, take an appropriate halogenated benzene derivative and replace the halogen atom on it with a nucleophilic reagent. In the reaction, choose a suitable nucleophilic reagent, depending on the activity of the halogen atom and the structure of the substrate. Controlling the reaction conditions, such as temperature, solvent, type and dosage of base, etc., all affect the success or failure of the reaction and the yield. If the temperature is too high or the side reactions increase, if it is too low, the reaction rate will be delayed. Choosing a suitable solvent can help the reactants dissolve and promote the smooth progress of the reaction. The base can activate the nucleophilic reagent, and the dosage needs to be precisely regulated to prevent overreaction.
Second, through the direct fluorination reaction of aromatic hydrocarbons. Using a specific fluorination reagent, fluorine atoms are introduced at a specific position on the benzene ring. In this process, the selection of fluorination reagents is crucial. Different fluorination reagents have different activities and selectivity. To introduce fluorine atoms precisely into the 2,4 positions, reagents with high regional selectivity need to be selected. At the same time, the acidity of the reaction system, reaction time and other factors also have a great impact on the reaction. Improper acidity may affect the activity and selectivity of the reagent; if the reaction time is too short, the fluorination is incomplete; if it is too long, it may cause excessive fluorination and other side reactions.
Third, the target molecule is constructed in a multi-step reaction. The benzene ring intermediate containing some substituents is synthesized first, and then the rest of the substituents are introduced after gradual modification. This strategy requires careful planning of the reaction sequence and consideration of the interaction between each step of the reaction. If the substituent is introduced first, it may affect the activity and selectivity of the subsequent reaction. After each step of the reaction, the intermediate needs to be properly separated and purified to ensure the smooth reaction of the next step.
All these methods have advantages and disadvantages. In the actual synthesis, it is necessary to consider the availability of raw materials, cost, and the ease of control of the reaction conditions. It is a good policy to make the reaction efficient and economical, and to minimize the generation of side reactions and waste as much as possible.
First, it can be prepared from halogenated aromatics by nucleophilic substitution reaction. First, take an appropriate halogenated benzene derivative and replace the halogen atom on it with a nucleophilic reagent. In the reaction, choose a suitable nucleophilic reagent, depending on the activity of the halogen atom and the structure of the substrate. Controlling the reaction conditions, such as temperature, solvent, type and dosage of base, etc., all affect the success or failure of the reaction and the yield. If the temperature is too high or the side reactions increase, if it is too low, the reaction rate will be delayed. Choosing a suitable solvent can help the reactants dissolve and promote the smooth progress of the reaction. The base can activate the nucleophilic reagent, and the dosage needs to be precisely regulated to prevent overreaction.
Second, through the direct fluorination reaction of aromatic hydrocarbons. Using a specific fluorination reagent, fluorine atoms are introduced at a specific position on the benzene ring. In this process, the selection of fluorination reagents is crucial. Different fluorination reagents have different activities and selectivity. To introduce fluorine atoms precisely into the 2,4 positions, reagents with high regional selectivity need to be selected. At the same time, the acidity of the reaction system, reaction time and other factors also have a great impact on the reaction. Improper acidity may affect the activity and selectivity of the reagent; if the reaction time is too short, the fluorination is incomplete; if it is too long, it may cause excessive fluorination and other side reactions.
Third, the target molecule is constructed in a multi-step reaction. The benzene ring intermediate containing some substituents is synthesized first, and then the rest of the substituents are introduced after gradual modification. This strategy requires careful planning of the reaction sequence and consideration of the interaction between each step of the reaction. If the substituent is introduced first, it may affect the activity and selectivity of the subsequent reaction. After each step of the reaction, the intermediate needs to be properly separated and purified to ensure the smooth reaction of the next step.
All these methods have advantages and disadvantages. In the actual synthesis, it is necessary to consider the availability of raw materials, cost, and the ease of control of the reaction conditions. It is a good policy to make the reaction efficient and economical, and to minimize the generation of side reactions and waste as much as possible.
What are the precautions for storing and transporting 2,4-dichloro-1-methyl-3-nitro-5- (trifluoromethyl) benzene?
2% 2C4-difluoro-1-methyl-3-pyridine-5 - (trifluoromethyl) benzene is an extremely rare and unique chemical. When storing and transporting these substances, the following things must be taken care of:
First, the storage place must be dry and cool. Because it is extremely sensitive to moisture and high temperature, moisture can easily cause adverse reactions such as hydrolysis, and high temperature may cause changes in its chemical properties, or even lead to dangerous chemical reactions. Therefore, a dry warehouse with good ventilation and temperature maintained at a specific range (such as 5 ° C - 25 ° C) should be selected.
Second, the fire source and oxidant must be strictly isolated. Many of these chemicals are flammable or prone to violent reactions after contact with oxidants, so fireworks are strictly prohibited in the storage area, and they cannot be stored in the same place as oxidants. Be sure to keep a certain safe distance.
Third, when transporting, the packaging must be strong and well sealed. Choose suitable packaging materials, such as special corrosion-resistant and pressure-resistant containers, to prevent packaging damage due to bumps and collisions during transportation, which may lead to leakage. And the transportation vehicle must also be equipped with corresponding emergency treatment equipment and protective equipment.
Fourth, the operator and the person in contact must wear professional protective equipment. Such as protective gloves, goggles, protective clothing, etc., to avoid contact with the skin and eyes, because it may be irritating and toxic, after accidental contact or cause serious damage to the human body.
Fifth, storage and transportation places should be set up with prominent warning signs. Clearly indicate the danger of the substance so that relevant personnel are always vigilant, and should formulate a sound emergency plan, in the event of an accident, can quickly and effectively respond.
First, the storage place must be dry and cool. Because it is extremely sensitive to moisture and high temperature, moisture can easily cause adverse reactions such as hydrolysis, and high temperature may cause changes in its chemical properties, or even lead to dangerous chemical reactions. Therefore, a dry warehouse with good ventilation and temperature maintained at a specific range (such as 5 ° C - 25 ° C) should be selected.
Second, the fire source and oxidant must be strictly isolated. Many of these chemicals are flammable or prone to violent reactions after contact with oxidants, so fireworks are strictly prohibited in the storage area, and they cannot be stored in the same place as oxidants. Be sure to keep a certain safe distance.
Third, when transporting, the packaging must be strong and well sealed. Choose suitable packaging materials, such as special corrosion-resistant and pressure-resistant containers, to prevent packaging damage due to bumps and collisions during transportation, which may lead to leakage. And the transportation vehicle must also be equipped with corresponding emergency treatment equipment and protective equipment.
Fourth, the operator and the person in contact must wear professional protective equipment. Such as protective gloves, goggles, protective clothing, etc., to avoid contact with the skin and eyes, because it may be irritating and toxic, after accidental contact or cause serious damage to the human body.
Fifth, storage and transportation places should be set up with prominent warning signs. Clearly indicate the danger of the substance so that relevant personnel are always vigilant, and should formulate a sound emergency plan, in the event of an accident, can quickly and effectively respond.
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