Linshang Chemical
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2,3-Dichloro-4-Methyl-1-Nitro-5-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
160374 |
| Chemical Formula | C7H3Cl2F3NO2 |
| Molar Mass | 260.003 g/mol |
As an accredited 2,3-Dichloro-4-Methyl-1-Nitro-5-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 2,3 - dichloro - 4 - methyl - 1 - nitro - 5 - (trifluoromethyl)benzene in sealed chemical - grade packaging. |
| Storage | 2,3 - dichloro - 4 - methyl - 1 - nitro - 5 - (trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials, to prevent leakage. Store it separately from incompatible substances such as oxidizing agents and reducing agents to avoid potential reactions. |
| Shipping | 2,3 - dichloro - 4 - methyl - 1 - nitro - 5 - (trifluoromethyl)benzene is a chemical. It should be shipped in accordance with hazardous chemical regulations, using proper packaging to prevent leakage and ensure safe transportation. |
Competitive 2,3-Dichloro-4-Methyl-1-Nitro-5-(Trifluoromethyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 2,3-Dichloro-4-Methyl-1-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 2,3-dichloro-4-methyl-1-nitro-5- (trifluoromethyl) benzene?
2% 2C3 + - + dioxy + - + 4 + - + methyl + - + 1 + - + cyano + - + 5 + - + (trichloromethyl) benzene is a key raw material for organic synthesis and has important uses in many fields such as medicine, pesticides, and materials.
In the field of medicine, it can be used as a key intermediate for the synthesis of a variety of drugs. For example, some antibacterial drugs, with their special chemical structures, can effectively inhibit the growth and reproduction of bacteria, which is of great significance for the treatment of various infectious diseases. Or in the synthesis of anti-tumor drugs, it participates in the construction of specific structures that help drugs to precisely act on tumor cells, inhibit tumor growth and spread, and provide effective means for cancer treatment.
In the field of pesticides, 2% 2C3 + - + dioxygen + - + 4 + - + methyl + - + 1 + - + cyano + - + 5 + - + (trichloromethyl) benzene is also indispensable. It can be used to create new pesticides, which have efficient killing or repelling effects on pests. Due to its structural characteristics, it can interfere with the normal physiological metabolism of pests, destroy their nervous system or respiratory system, so as to achieve good insect control and pest control effects, ensure the healthy growth of crops, and improve the yield and quality of agricultural products.
In the field of materials, it can be used as a synthetic monomer of functional materials. After polymerization, it is combined with other monomers to give the material unique properties. For example, synthesizing polymer materials with special optical, electrical or thermal properties can be used in electronic devices, optical instruments and other fields. It can make electronic devices have better conductivity and stability, or make optical instruments have better optical transmittance and anti-aging properties.
2% 2C3 + - + dioxy + - + 4 + - + methyl + - + 1 + - + cyano + - + 5 + - + (trichloromethyl) benzene With its unique chemical structure, it plays an important role in many fields and promotes the continuous development and progress of related industries.
In the field of medicine, it can be used as a key intermediate for the synthesis of a variety of drugs. For example, some antibacterial drugs, with their special chemical structures, can effectively inhibit the growth and reproduction of bacteria, which is of great significance for the treatment of various infectious diseases. Or in the synthesis of anti-tumor drugs, it participates in the construction of specific structures that help drugs to precisely act on tumor cells, inhibit tumor growth and spread, and provide effective means for cancer treatment.
In the field of pesticides, 2% 2C3 + - + dioxygen + - + 4 + - + methyl + - + 1 + - + cyano + - + 5 + - + (trichloromethyl) benzene is also indispensable. It can be used to create new pesticides, which have efficient killing or repelling effects on pests. Due to its structural characteristics, it can interfere with the normal physiological metabolism of pests, destroy their nervous system or respiratory system, so as to achieve good insect control and pest control effects, ensure the healthy growth of crops, and improve the yield and quality of agricultural products.
In the field of materials, it can be used as a synthetic monomer of functional materials. After polymerization, it is combined with other monomers to give the material unique properties. For example, synthesizing polymer materials with special optical, electrical or thermal properties can be used in electronic devices, optical instruments and other fields. It can make electronic devices have better conductivity and stability, or make optical instruments have better optical transmittance and anti-aging properties.
2% 2C3 + - + dioxy + - + 4 + - + methyl + - + 1 + - + cyano + - + 5 + - + (trichloromethyl) benzene With its unique chemical structure, it plays an important role in many fields and promotes the continuous development and progress of related industries.
What are the physical properties of 2,3-dichloro-4-methyl-1-nitro-5- (trifluoromethyl) benzene
2% 2C3-dioxy-4-methyl-1-naphthyl-5- (trifluoromethyl) quinoline is a compound with considerable characteristics in the field of organic synthesis. Its physical properties are particularly important, and it is related to its performance in various reactions and applications.
Looking at its appearance, it often takes a solid form, mostly white to light yellow powdered substances. This form is easy to store and use, and can reflect its intermolecular interaction and aggregation state to a certain extent.
When it comes to melting point, due to the existence of different groups such as dioxy, methyl, naphthyl and trifluoromethyl in the molecular structure, these groups interact with each other, making the compound have a relatively high melting point. Specifically, under standard pressure, its melting point is in a certain temperature range, which is of great significance in the synthesis and purification process for controlling its phase transition, and its purity can be judged by melting point measurement.
In terms of solubility, considering that there are both hydrophobic parts containing hydrocarbons in the molecule, such as naphthalene groups, methyl groups, and special groups containing fluorine, trifluoromethyl groups, and dioxy structures with certain polarities, the dissolution behavior in organic solvents is quite unique. In halogenated hydrocarbon organic solvents such as dichloromethane and chloroform, it exhibits good solubility, which is due to the van der Waals force and partial polar interaction between halogenated hydrocarbons and compound molecules; while in water with strong polarity, its solubility is very small. Due to the large proportion of the hydrophobic part of the molecule as a whole, it is difficult to form an effective interaction with water molecules.
In addition, the density of the compound is also an important physical property. Due to the presence of fluorine atoms in the molecule, the fluorine atoms have a larger relative atomic mass and a smaller atomic radius, resulting in an increase in the weight of the whole molecule and a more compact spatial arrangement, which in turn leads to a higher density than that of compounds of the same type that do not contain fluorine. This density characteristic needs to be taken into account when it involves separation, extraction, etc., which is of great significance for judging its distribution and behavior in different media.
Looking at its appearance, it often takes a solid form, mostly white to light yellow powdered substances. This form is easy to store and use, and can reflect its intermolecular interaction and aggregation state to a certain extent.
When it comes to melting point, due to the existence of different groups such as dioxy, methyl, naphthyl and trifluoromethyl in the molecular structure, these groups interact with each other, making the compound have a relatively high melting point. Specifically, under standard pressure, its melting point is in a certain temperature range, which is of great significance in the synthesis and purification process for controlling its phase transition, and its purity can be judged by melting point measurement.
In terms of solubility, considering that there are both hydrophobic parts containing hydrocarbons in the molecule, such as naphthalene groups, methyl groups, and special groups containing fluorine, trifluoromethyl groups, and dioxy structures with certain polarities, the dissolution behavior in organic solvents is quite unique. In halogenated hydrocarbon organic solvents such as dichloromethane and chloroform, it exhibits good solubility, which is due to the van der Waals force and partial polar interaction between halogenated hydrocarbons and compound molecules; while in water with strong polarity, its solubility is very small. Due to the large proportion of the hydrophobic part of the molecule as a whole, it is difficult to form an effective interaction with water molecules.
In addition, the density of the compound is also an important physical property. Due to the presence of fluorine atoms in the molecule, the fluorine atoms have a larger relative atomic mass and a smaller atomic radius, resulting in an increase in the weight of the whole molecule and a more compact spatial arrangement, which in turn leads to a higher density than that of compounds of the same type that do not contain fluorine. This density characteristic needs to be taken into account when it involves separation, extraction, etc., which is of great significance for judging its distribution and behavior in different media.
Is the chemical properties of 2,3-dichloro-4-methyl-1-nitro-5- (trifluoromethyl) benzene stable?
The chemical properties of 2% 2C3-dioxy-4-methyl-1-furan-5 - (trifluoromethyl) pyridine are relatively stable.
From its structural point of view, the dioxy structure part, due to the high electronegativity of the oxygen atom, will affect the distribution of the surrounding electron cloud, so that the region presents a certain polarity, which contributes to the intermolecular force, which in turn affects its physical and chemical properties. However, the dioxy structure itself forms a stable ring and has a certain rigidity, which can enhance the stability of the whole molecule. The presence of
4-methyl, with methyl as the power supply group, will provide an electron cloud to the pyridine ring, change the electron cloud density distribution of the pyridine ring, and change the reactivity at a specific position on the pyridine ring. However, the overall methyl group has little effect on the structural stability, which can increase the lipid solubility of the molecule to a certain extent.
1-furan ring, as an aromatic heterocyclic structure, its conjugate system helps to stabilize the overall electron cloud of the molecule, and the oxygen atoms on the furan ring interact with other atoms to further stabilize the molecular structure.
5- (trifluoromethyl) pyridine moiety, trifluoromethyl is a strong electron-absorbing group, which has a strong attraction to the electron cloud of the pyridine ring, which can adjust the electronic properties of the pyridine ring. The pyridine ring itself has a certain alkalinity, and the introduction of trifluoromethyl will change its alkaline strength. At the same time, the strong electronegative fluorine atom of trifluoromethyl, due to the high C-F bond energy, makes the structure of this part relatively stable, which is not prone to general chemical reactions, and enhances the chemical stability of the whole compound. Combining the interaction of various parts of the structure, this compound is chemically stable under common conditions, is not prone to spontaneous decomposition, rearrangement and other reactions, and can resist the attack of common chemical reagents to a certain extent. It can maintain structural integrity in a variety of environments.
From its structural point of view, the dioxy structure part, due to the high electronegativity of the oxygen atom, will affect the distribution of the surrounding electron cloud, so that the region presents a certain polarity, which contributes to the intermolecular force, which in turn affects its physical and chemical properties. However, the dioxy structure itself forms a stable ring and has a certain rigidity, which can enhance the stability of the whole molecule. The presence of
4-methyl, with methyl as the power supply group, will provide an electron cloud to the pyridine ring, change the electron cloud density distribution of the pyridine ring, and change the reactivity at a specific position on the pyridine ring. However, the overall methyl group has little effect on the structural stability, which can increase the lipid solubility of the molecule to a certain extent.
1-furan ring, as an aromatic heterocyclic structure, its conjugate system helps to stabilize the overall electron cloud of the molecule, and the oxygen atoms on the furan ring interact with other atoms to further stabilize the molecular structure.
5- (trifluoromethyl) pyridine moiety, trifluoromethyl is a strong electron-absorbing group, which has a strong attraction to the electron cloud of the pyridine ring, which can adjust the electronic properties of the pyridine ring. The pyridine ring itself has a certain alkalinity, and the introduction of trifluoromethyl will change its alkaline strength. At the same time, the strong electronegative fluorine atom of trifluoromethyl, due to the high C-F bond energy, makes the structure of this part relatively stable, which is not prone to general chemical reactions, and enhances the chemical stability of the whole compound. Combining the interaction of various parts of the structure, this compound is chemically stable under common conditions, is not prone to spontaneous decomposition, rearrangement and other reactions, and can resist the attack of common chemical reagents to a certain extent. It can maintain structural integrity in a variety of environments.
What are the synthesis methods of 2,3-dichloro-4-methyl-1-nitro-5- (trifluoromethyl) benzene
The synthesis method of 2% 2C3-dioxy-4-methyl-1-carbonyl-5- (trifluoromethyl) benzene can be found from the concept of "Tiangong Kaiwu" and the idea of ancient chemical techniques.
First, we can learn from the method of using natural substances as starting materials in ancient methods. Find natural fragrances or plant extracts containing corresponding structural fragments, such as some plant components with aromatic ring structures. Use mild extraction methods, such as water or alcohol as solvents, to obtain crude extracts by dipping, percolation, etc. Then purify by distillation and sublimation of ancient methods. Later, according to the chemical reactions mentioned in ancient books, such as acetic anhydride, alkali and other common reagents, through acylation, substitution and other reactions, groups such as dioxy, methyl, carbonyl and trifluoromethyl are gradually introduced.
Second, simulate the chemical reactions of ancient alchemy. There are many reactions catalyzed by metal salts in alchemy. The metal catalysts mentioned in the ancient recipe can be found, such as lead Dan, mercury salts, etc. (modern experiments need to pay attention to their toxicity and substitutes), to catalyze simple compounds containing benzene rings. By heating, roasting and other conditions similar to alchemy, the compound is promoted to undergo cyclization and substitution reactions. For example, benzene derivatives react with halogenated hydrocarbons (containing methyl and trifluoromethyl) under the catalysis of metal salts and high temperature, and introduce corresponding groups. Control the reaction temperature and time, and adjust the reaction process according to the concept of heat control in ancient books, or by observing reaction phenomena, such as color change, gas escape, etc.
Third, refer to the idea of ancient dyeing processes. In ancient dyeing, mordants were often used to combine dyes with fabrics. The construction of the target compound can be regarded as a "dyeing" process. Reagents containing specific groups are used as "dyes", benzene derivatives with active check points are used as "fabrics", and mordant-like substances, such as certain organic acids or metal complexes, are introduced. In suitable solvents, such as rice wine and tung oil commonly used in ancient recipes, the combination of the two is promoted. The synthesis of 2% 2C3-dioxy-4-methyl-1-carbonyl-5- (trifluoromethyl) benzene was achieved by adjusting the dosage of mordant, reaction solvent and temperature.
First, we can learn from the method of using natural substances as starting materials in ancient methods. Find natural fragrances or plant extracts containing corresponding structural fragments, such as some plant components with aromatic ring structures. Use mild extraction methods, such as water or alcohol as solvents, to obtain crude extracts by dipping, percolation, etc. Then purify by distillation and sublimation of ancient methods. Later, according to the chemical reactions mentioned in ancient books, such as acetic anhydride, alkali and other common reagents, through acylation, substitution and other reactions, groups such as dioxy, methyl, carbonyl and trifluoromethyl are gradually introduced.
Second, simulate the chemical reactions of ancient alchemy. There are many reactions catalyzed by metal salts in alchemy. The metal catalysts mentioned in the ancient recipe can be found, such as lead Dan, mercury salts, etc. (modern experiments need to pay attention to their toxicity and substitutes), to catalyze simple compounds containing benzene rings. By heating, roasting and other conditions similar to alchemy, the compound is promoted to undergo cyclization and substitution reactions. For example, benzene derivatives react with halogenated hydrocarbons (containing methyl and trifluoromethyl) under the catalysis of metal salts and high temperature, and introduce corresponding groups. Control the reaction temperature and time, and adjust the reaction process according to the concept of heat control in ancient books, or by observing reaction phenomena, such as color change, gas escape, etc.
Third, refer to the idea of ancient dyeing processes. In ancient dyeing, mordants were often used to combine dyes with fabrics. The construction of the target compound can be regarded as a "dyeing" process. Reagents containing specific groups are used as "dyes", benzene derivatives with active check points are used as "fabrics", and mordant-like substances, such as certain organic acids or metal complexes, are introduced. In suitable solvents, such as rice wine and tung oil commonly used in ancient recipes, the combination of the two is promoted. The synthesis of 2% 2C3-dioxy-4-methyl-1-carbonyl-5- (trifluoromethyl) benzene was achieved by adjusting the dosage of mordant, reaction solvent and temperature.
Precautions for storing and transporting 2,3-dichloro-4-methyl-1-nitro-5- (trifluoromethyl) benzene
2% 2C3-dioxy-4-methyl-1-naphthyl-5- (trifluoromethyl) benzene is a major step in storage and transportation, and many key precautions need to be taken with caution.
First, this material has special properties and is extremely sensitive to the temperature and humidity of the storage environment. If the temperature is too high, it may cause chemical reactions to destroy its chemical structure; if the humidity is too high, it may cause deliquescence, which affects its purity and quality. Therefore, it should be stored in a dry, cool and well-ventilated place. The temperature should be constant within a specific range, and the humidity should be strictly controlled to prevent its properties from changing.
Second, when transporting, it is necessary to follow strict transportation regulations because it may be dangerous. The packaging must be solid and well sealed to prevent leakage due to bumps and collisions during transportation. And according to its dangerous characteristics, it is necessary to configure corresponding warning labels to inform transporters and related personnel of the latent risk.
Third, this chemical substance may be incompatible with other substances. During storage and transportation, it must not be mixed with substances that are prone to reactions. It is necessary to have a detailed understanding of its chemical properties, and to clarify the substances that are incompatible with it, so as to avoid dangerous chemical reactions caused by wrong placement, such as severe combustion, explosion and other serious consequences.
Fourth, whether it is storage or transportation, it is necessary to have complete records and supervision. Record its warehousing time, quantity, storage conditions and transportation routes and other information for traceability and monitoring at any time. At the same time, relevant operators need to be professionally trained, familiar with the operation process and emergency treatment measures, and can respond quickly and properly in case of emergencies to minimize the harm. In this way, the safety of 2% 2C3-dioxy-4-methyl-1-naphthyl-5 - (trifluoromethyl) benzene during storage and transportation can be ensured.
First, this material has special properties and is extremely sensitive to the temperature and humidity of the storage environment. If the temperature is too high, it may cause chemical reactions to destroy its chemical structure; if the humidity is too high, it may cause deliquescence, which affects its purity and quality. Therefore, it should be stored in a dry, cool and well-ventilated place. The temperature should be constant within a specific range, and the humidity should be strictly controlled to prevent its properties from changing.
Second, when transporting, it is necessary to follow strict transportation regulations because it may be dangerous. The packaging must be solid and well sealed to prevent leakage due to bumps and collisions during transportation. And according to its dangerous characteristics, it is necessary to configure corresponding warning labels to inform transporters and related personnel of the latent risk.
Third, this chemical substance may be incompatible with other substances. During storage and transportation, it must not be mixed with substances that are prone to reactions. It is necessary to have a detailed understanding of its chemical properties, and to clarify the substances that are incompatible with it, so as to avoid dangerous chemical reactions caused by wrong placement, such as severe combustion, explosion and other serious consequences.
Fourth, whether it is storage or transportation, it is necessary to have complete records and supervision. Record its warehousing time, quantity, storage conditions and transportation routes and other information for traceability and monitoring at any time. At the same time, relevant operators need to be professionally trained, familiar with the operation process and emergency treatment measures, and can respond quickly and properly in case of emergencies to minimize the harm. In this way, the safety of 2% 2C3-dioxy-4-methyl-1-naphthyl-5 - (trifluoromethyl) benzene during storage and transportation can be ensured.
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