Linshang Chemical
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2,3-Dichloro-4-Methyl-5-Nitro-1-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
943632 |
| Chemical Formula | C8H3Cl2F3NO2 |
| Molar Mass | 274.01 g/mol |
| Appearance | Solid (predicted) |
| Boiling Point | No data |
| Melting Point | No data |
| Density | No data |
| Solubility In Water | Insoluble (predicted) |
| Vapor Pressure | No data |
| Logp | No data |
| Pka | No data |
As an accredited 2,3-Dichloro-4-Methyl-5-Nitro-1-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,3 - dichloro - 4 - methyl - 5 - nitro - 1 - (trifluoromethyl)benzene in sealed chemical - grade bottle. |
| Storage | 2,3 - dichloro - 4 - methyl - 5 - nitro - 1 - (trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly sealed container, preferably made of corrosion - resistant material, to prevent leakage and protect from environmental factors that could initiate reactions. |
| Shipping | 2,3 - dichloro - 4 - methyl - 5 - nitro - 1 - (trifluoromethyl)benzene is shipped in specialized, leak - proof containers. It adheres to strict chemical shipping regulations, ensuring secure transportation to prevent any environmental or safety risks. |
Competitive 2,3-Dichloro-4-Methyl-5-Nitro-1-(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
Where to Buy 2,3-Dichloro-4-Methyl-5-Nitro-1-(Trifluoromethyl)Benzene in China?
As a trusted 2,3-Dichloro-4-Methyl-5-Nitro-1-(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 2,3-Dichloro-4-Methyl-5-Nitro-1-(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 2,3-dichloro-4-methyl-5-nitro-1- (trifluoromethyl) benzene?
2% 2C3-difluoro-4-methyl-5-chloro-1- (trifluoromethyl) benzene has a wide range of uses. In the field of pharmaceutical synthesis, it can be used as a key intermediate. Due to its specific chemical structure, it can participate in a variety of complex organic reactions and help synthesize drug molecules with specific physiological activities, which is of great significance to the creation of new drugs.
In the field of materials science, it also has outstanding performance. It can be used as a raw material for the synthesis of special polymer materials, and can be polymerized to form polymers with unique properties. Such polymers may have excellent heat resistance and chemical stability, and can be used in aerospace, electronics and other fields that require strict material properties.
In pesticide research and development, 2% 2C3-difluoro-4-methyl-5-chloro-1- (trifluoromethyl) benzene also plays an important role. With its structural characteristics, pesticide ingredients with high-efficiency insecticidal and bactericidal activities can be synthesized, providing a powerful means for agricultural pest control, and can reduce the adverse impact on the environment while ensuring the efficacy, which is in line with the current needs of green agriculture development.
In conclusion, 2% 2C3-difluoro-4-methyl-5-chloro-1 - (trifluoromethyl) benzene, with its unique chemical structure, has shown great application value in many fields such as medicine, materials, and pesticides, and has played a significant role in promoting the development of related industries.
In the field of materials science, it also has outstanding performance. It can be used as a raw material for the synthesis of special polymer materials, and can be polymerized to form polymers with unique properties. Such polymers may have excellent heat resistance and chemical stability, and can be used in aerospace, electronics and other fields that require strict material properties.
In pesticide research and development, 2% 2C3-difluoro-4-methyl-5-chloro-1- (trifluoromethyl) benzene also plays an important role. With its structural characteristics, pesticide ingredients with high-efficiency insecticidal and bactericidal activities can be synthesized, providing a powerful means for agricultural pest control, and can reduce the adverse impact on the environment while ensuring the efficacy, which is in line with the current needs of green agriculture development.
In conclusion, 2% 2C3-difluoro-4-methyl-5-chloro-1 - (trifluoromethyl) benzene, with its unique chemical structure, has shown great application value in many fields such as medicine, materials, and pesticides, and has played a significant role in promoting the development of related industries.
What are the physical properties of 2,3-dichloro-4-methyl-5-nitro-1- (trifluoromethyl) benzene?
2% 2C3 -difluoro-4-methyl-5-methoxy-1 - (trifluoromethyl) benzene organic compound, its physical properties are as follows:
This compound is mostly colorless to light yellow liquid under normal conditions, with a special odor. Due to the strong electronegativity of fluorine atoms in the molecule, it has high stability and chemical inertness, and can resist the invasion of many chemical reactions.
Its boiling point is relatively high due to the influence of intermolecular forces, and the specific value depends on the complex interaction between molecules. Due to the influence of molecular polarity, it has good solubility in common organic solvents such as ethanol and acetone, which can form a suitable interaction between molecules and solvent molecules and help them disperse uniformly.
The compound has a higher density than water. If placed in water, it will sink to the bottom. At the same time, because of its fluoride atom, it has a certain potential impact on the environment, high stability in the environment, and difficult to degrade naturally. It should be treated with caution when using and handling, and follow relevant environmental protection regulations and operating procedures to prevent adverse consequences to the ecological environment.
This compound is mostly colorless to light yellow liquid under normal conditions, with a special odor. Due to the strong electronegativity of fluorine atoms in the molecule, it has high stability and chemical inertness, and can resist the invasion of many chemical reactions.
Its boiling point is relatively high due to the influence of intermolecular forces, and the specific value depends on the complex interaction between molecules. Due to the influence of molecular polarity, it has good solubility in common organic solvents such as ethanol and acetone, which can form a suitable interaction between molecules and solvent molecules and help them disperse uniformly.
The compound has a higher density than water. If placed in water, it will sink to the bottom. At the same time, because of its fluoride atom, it has a certain potential impact on the environment, high stability in the environment, and difficult to degrade naturally. It should be treated with caution when using and handling, and follow relevant environmental protection regulations and operating procedures to prevent adverse consequences to the ecological environment.
Is 2,3-dichloro-4-methyl-5-nitro-1- (trifluoromethyl) benzene chemically stable?
The chemical properties of 2% 2C3-difluoro-4-methyl-5-chloro-1- (trifluoromethyl) benzene are relatively stable. This is due to the highly conjugated system of the benzene ring structure, which endows it with special stability. The benzene ring is connected by six carbon atoms with a unique conjugated π bond to form a closed conjugated system. The electron cloud is uniformly distributed over the entire ring, which makes the benzene ring have a low energy state and is not easy to participate in chemical reactions.
In this compound, although a variety of halogen atoms and methyl groups are introduced, the influence of these substituents on the benzene ring conjugated system is limited. Although the halogen atom has a certain electron-withdrawing induction effect, it also has a donor-electron conjugation effect. The interaction between the two has little change in the electron cloud density of the benzene ring. Methyl group is the power supply group, which can increase the electron cloud density of the benzene ring and stabilize the benzene ring to a certain extent. Furthermore, when the halogen atom is connected to the benzene ring, the lone pair electrons of the halogen atom can form p-π conjugate with the π electrons of the benzene ring, further stabilizing the molecular structure. Due to the above factors, 2% 2C3-difluoro-4-methyl-5-chloro-1- (trifluoromethyl) benzene has relatively stable chemical properties, and it is difficult to undergo chemical reactions under normal conditions. It can maintain a relatively stable state in common environments.
In this compound, although a variety of halogen atoms and methyl groups are introduced, the influence of these substituents on the benzene ring conjugated system is limited. Although the halogen atom has a certain electron-withdrawing induction effect, it also has a donor-electron conjugation effect. The interaction between the two has little change in the electron cloud density of the benzene ring. Methyl group is the power supply group, which can increase the electron cloud density of the benzene ring and stabilize the benzene ring to a certain extent. Furthermore, when the halogen atom is connected to the benzene ring, the lone pair electrons of the halogen atom can form p-π conjugate with the π electrons of the benzene ring, further stabilizing the molecular structure. Due to the above factors, 2% 2C3-difluoro-4-methyl-5-chloro-1- (trifluoromethyl) benzene has relatively stable chemical properties, and it is difficult to undergo chemical reactions under normal conditions. It can maintain a relatively stable state in common environments.
What are the methods for preparing 2,3-dichloro-4-methyl-5-nitro-1- (trifluoromethyl) benzene?
To prepare 2,3-dideuterium-4-methyl-5-hydroxy-1- (trideuterium-methyl) benzene, the following ancient methods can be used.
The method of nucleophilic substitution is first proposed. Choose a suitable halogenated aromatic hydrocarbon, whose halogen atom is attached to the benzene ring, and the benzene ring has corresponding methyl, hydroxyl and other substituents. Using deuterium-containing reagents, such as deuterium-substituted alkoxides, deuterium-substituted amines, etc., as nucleophiles, in appropriate solvents, such as polar aprotic solvents, such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), heating or under the help of catalysts, nucleophiles attack the carbon attached to the halogen atom of halogenated aromatics, and the halogen atom leaves, thereby introducing deuterium atoms and desired groups. This process requires fine regulation of reaction temperature, time and reagent dosage to achieve high yield and high selectivity.
In addition, it is possible to consider the technique of reducing deuteration. If there are groups that can be reduced on the benzene ring, such as nitro, carbonyl, etc. First, deuterate with suitable deuterium-containing reducing agents, such as deuterium replaced by sodium borohydride (NaBD) and deuterium replaced by lithium aluminum hydride (LiAlD). If there is a nitro group on the benzene ring, the nitro group can be gradually reduced to an amino group through the action of a deuterated reducing agent, and deuterium atoms can be introduced at the same time. After that, the amino group and other groups can be further converted according to demand to obtain the target product. However, when using such strong reducing agents, it is necessary to pay attention to the mildness of the reaction conditions to avoid overreaction.
Or the method of constructing aromatic rings can be used. Using small molecules containing specific substituents as raw materials, deuterium atoms and required methyl, hydroxyl and other groups are introduced into the benzene ring through reactions such as the Friedel-Crafts reaction. For example, with appropriate deuterium-containing halogenated hydrocarbons and hydroxyl-containing aromatic hydrocarbon precursors, under the catalysis of Lewis acid catalysts, such as anhydrous aluminum trichloride (AlCl 🥰), the Fu-gram alkylation reaction is carried out to construct the target benzene ring structure. In this process, the amount of catalyst and the proportion of reaction substrates have a great influence on the reaction results, and it needs to be considered in detail.
The method of nucleophilic substitution is first proposed. Choose a suitable halogenated aromatic hydrocarbon, whose halogen atom is attached to the benzene ring, and the benzene ring has corresponding methyl, hydroxyl and other substituents. Using deuterium-containing reagents, such as deuterium-substituted alkoxides, deuterium-substituted amines, etc., as nucleophiles, in appropriate solvents, such as polar aprotic solvents, such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), heating or under the help of catalysts, nucleophiles attack the carbon attached to the halogen atom of halogenated aromatics, and the halogen atom leaves, thereby introducing deuterium atoms and desired groups. This process requires fine regulation of reaction temperature, time and reagent dosage to achieve high yield and high selectivity.
In addition, it is possible to consider the technique of reducing deuteration. If there are groups that can be reduced on the benzene ring, such as nitro, carbonyl, etc. First, deuterate with suitable deuterium-containing reducing agents, such as deuterium replaced by sodium borohydride (NaBD) and deuterium replaced by lithium aluminum hydride (LiAlD). If there is a nitro group on the benzene ring, the nitro group can be gradually reduced to an amino group through the action of a deuterated reducing agent, and deuterium atoms can be introduced at the same time. After that, the amino group and other groups can be further converted according to demand to obtain the target product. However, when using such strong reducing agents, it is necessary to pay attention to the mildness of the reaction conditions to avoid overreaction.
Or the method of constructing aromatic rings can be used. Using small molecules containing specific substituents as raw materials, deuterium atoms and required methyl, hydroxyl and other groups are introduced into the benzene ring through reactions such as the Friedel-Crafts reaction. For example, with appropriate deuterium-containing halogenated hydrocarbons and hydroxyl-containing aromatic hydrocarbon precursors, under the catalysis of Lewis acid catalysts, such as anhydrous aluminum trichloride (AlCl 🥰), the Fu-gram alkylation reaction is carried out to construct the target benzene ring structure. In this process, the amount of catalyst and the proportion of reaction substrates have a great influence on the reaction results, and it needs to be considered in detail.
What are the precautions for storing and transporting 2,3-dichloro-4-methyl-5-nitro-1- (trifluoromethyl) benzene?
2% 2C3-difluoro-4-methyl-5-methoxy-1- (trifluoromethyl) benzene requires attention to many key matters during storage and transportation.
First, because it is a chemical substance, it has strict requirements on the storage environment. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. This is because high temperature or open flame can easily cause chemical reactions, and even cause the risk of combustion and explosion. And the air humidity is too high, or it may react with moisture, causing the substance to deteriorate and damage its chemical properties and quality.
Second, the choice of storage container is also very critical. It is necessary to choose materials that are compatible with the substance, such as specific plastic or metal containers, to avoid chemical reactions between the container and the substance, causing corrosion or material contamination of the container. At the same time, the container must be well sealed to prevent the substance from evaporating or contacting with external substances.
Third, the transportation process should not be underestimated. Transportation vehicles must be equipped with corresponding fire protection and emergency treatment equipment to prevent sudden accidents during transportation. Transport personnel also need to be professionally trained to be familiar with the characteristics of the substance and emergency treatment methods. And when transporting, they should follow the specified route to avoid areas with dense traffic and people flow to reduce risks.
Fourth, handle it with care to avoid violent vibration and collision. Because the substance may cause unstable reactions under the action of vibration or collision. During operation, staff should also wear appropriate protective equipment, such as protective clothing, gloves, and goggles, to prevent substances from coming into contact with the skin and eyes and ensure personal safety.
First, because it is a chemical substance, it has strict requirements on the storage environment. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. This is because high temperature or open flame can easily cause chemical reactions, and even cause the risk of combustion and explosion. And the air humidity is too high, or it may react with moisture, causing the substance to deteriorate and damage its chemical properties and quality.
Second, the choice of storage container is also very critical. It is necessary to choose materials that are compatible with the substance, such as specific plastic or metal containers, to avoid chemical reactions between the container and the substance, causing corrosion or material contamination of the container. At the same time, the container must be well sealed to prevent the substance from evaporating or contacting with external substances.
Third, the transportation process should not be underestimated. Transportation vehicles must be equipped with corresponding fire protection and emergency treatment equipment to prevent sudden accidents during transportation. Transport personnel also need to be professionally trained to be familiar with the characteristics of the substance and emergency treatment methods. And when transporting, they should follow the specified route to avoid areas with dense traffic and people flow to reduce risks.
Fourth, handle it with care to avoid violent vibration and collision. Because the substance may cause unstable reactions under the action of vibration or collision. During operation, staff should also wear appropriate protective equipment, such as protective clothing, gloves, and goggles, to prevent substances from coming into contact with the skin and eyes and ensure personal safety.
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