Linshang Chemical
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1-Chloro-2-Nitro-4-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
151921 |
| Chemical Formula | C7H3ClF3NO2 |
| Molar Mass | 225.55 g/mol |
| Appearance | A colorless to pale yellow liquid |
| Boiling Point | Around 200 - 210 °C |
| Density | 1.53 - 1.55 g/cm³ |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene |
| Vapor Pressure | Low |
| Flash Point | Around 80 - 90 °C |
| Odor | Pungent |
As an accredited 1-Chloro-2-Nitro-4-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - chloro - 2 - nitro - 4 - (trifluoromethyl)benzene: Packed in 500 - gram bottles. |
| Storage | 1 - Chloro - 2 - nitro - 4 - (trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly sealed container to prevent leakage and exposure to air and moisture. Label the storage container clearly to avoid confusion. |
| Shipping | 1 - Chloro - 2 - nitro - 4 - (trifluoromethyl)benzene is a chemical that requires careful shipping. It must be in well - sealed, appropriate containers, following hazardous material regulations, ensuring safe transport to prevent spills and exposure. |
Competitive 1-Chloro-2-Nitro-4-(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.
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Tel: +8615365006308
Email: info@alchemist-chem.com
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As a leading 1-Chloro-2-Nitro-4-(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 1-chloro-2-nitro-4- (trifluoromethyl) benzene?
The main use of 1 + -tritium-2-amino-4- (triethoxy) silicon is to play a key role in many fields.
In the field of materials science, it can be used as a coupling agent. With its unique chemical structure, the amino group at one end can chemically react with materials containing polar groups such as hydroxyl and carboxyl groups, such as glass, ceramics, metal oxides, etc., to form stable chemical bonds; while the siloxane group at the other end can be hydrolyzed and condensed under specific conditions, and crosslinked with organic polymers, thereby strengthening the interfacial bonding force between inorganic materials and organic materials. In this way, the properties of composites can be significantly improved, such as improving the mechanical strength, water resistance, weather resistance, etc., and are widely used in the preparation of glass fiber reinforced plastics, coatings, adhesives and other products.
In the field of chemical synthesis, it plays an irreplaceable role as an important intermediate. Its amino and siloxane groups have high reactivity and can participate in a variety of organic synthesis reactions. By carefully designing the reaction path, it can be used to construct organosilicon compounds with special structures and functions. These compounds have broad application prospects in many fields such as medicine, pesticides, electronic chemicals, etc., such as the synthesis of drug molecules with specific biological activities or functional polymer materials.
In the field of surface modification, this substance also has important uses. Coating it on the surface of the material can give the material a new surface property. After the hydrolysis and condensation of the siloxane group, a siloxane film will be formed on the surface of the material, which will change the wettability and roughness of the material surface, so as to achieve the purpose of hydrophobic, hydrophilic, antifouling and other modification of the material surface. It is widely used in the surface treatment of textiles, paper, leather and other materials.
In the field of materials science, it can be used as a coupling agent. With its unique chemical structure, the amino group at one end can chemically react with materials containing polar groups such as hydroxyl and carboxyl groups, such as glass, ceramics, metal oxides, etc., to form stable chemical bonds; while the siloxane group at the other end can be hydrolyzed and condensed under specific conditions, and crosslinked with organic polymers, thereby strengthening the interfacial bonding force between inorganic materials and organic materials. In this way, the properties of composites can be significantly improved, such as improving the mechanical strength, water resistance, weather resistance, etc., and are widely used in the preparation of glass fiber reinforced plastics, coatings, adhesives and other products.
In the field of chemical synthesis, it plays an irreplaceable role as an important intermediate. Its amino and siloxane groups have high reactivity and can participate in a variety of organic synthesis reactions. By carefully designing the reaction path, it can be used to construct organosilicon compounds with special structures and functions. These compounds have broad application prospects in many fields such as medicine, pesticides, electronic chemicals, etc., such as the synthesis of drug molecules with specific biological activities or functional polymer materials.
In the field of surface modification, this substance also has important uses. Coating it on the surface of the material can give the material a new surface property. After the hydrolysis and condensation of the siloxane group, a siloxane film will be formed on the surface of the material, which will change the wettability and roughness of the material surface, so as to achieve the purpose of hydrophobic, hydrophilic, antifouling and other modification of the material surface. It is widely used in the surface treatment of textiles, paper, leather and other materials.
What are the physical properties of 1-chloro-2-nitro-4- (trifluoromethyl) benzene?
1 + -Deuterium-2 -amino-4- (triethylamino) benzene, its physical properties are as follows:
This substance is often solid, mostly white or almost white powder, fine and uniform. Its melting point is within a specific range, about [X] ° C to [X] ° C. The characteristics of the melting point are one of the important basis for the identification of this substance. In this temperature range, the substance gradually melts from solid to liquid, and the transition process is relatively smooth.
When it comes to solubility, it has a certain solubility in common organic solvents, such as ethanol and acetone. In ethanol, under normal temperature conditions, about [X] grams of this substance can be dissolved per 100 milliliters of ethanol. When dissolved, the substance can be observed to gradually disperse in the solvent, and the solution gradually clarifies. However, the solubility in water is relatively low, only about [X] grams per 100 milliliters of water can be dissolved, which is due to the fact that there are many hydrophobic groups in the molecular structure, so the hydrophilicity is poor.
Its density is about [X] grams per cubic centimeter, which is similar to the density of common organic compounds. With this density, if it is placed in a specific liquid, its density can be roughly inferred according to the floating condition.
Furthermore, the stability of this substance is quite considerable. Under normal temperature and pressure and without the interference of special chemical reagents, it can be stored for a long time without significant chemical changes. However, it should be noted that it is more sensitive to light, high temperature and strong acid and base environments. When the light is too strong or the temperature is too high, it may cause changes in the molecular structure, causing changes in its physical properties and chemical activities. When exposed to strong acids and bases, it is prone to chemical reactions, which in turn destroy its original structure.
The above physical properties are of crucial significance in many fields such as chemical production and drug research and development, and can be used for separation, purification and application.
This substance is often solid, mostly white or almost white powder, fine and uniform. Its melting point is within a specific range, about [X] ° C to [X] ° C. The characteristics of the melting point are one of the important basis for the identification of this substance. In this temperature range, the substance gradually melts from solid to liquid, and the transition process is relatively smooth.
When it comes to solubility, it has a certain solubility in common organic solvents, such as ethanol and acetone. In ethanol, under normal temperature conditions, about [X] grams of this substance can be dissolved per 100 milliliters of ethanol. When dissolved, the substance can be observed to gradually disperse in the solvent, and the solution gradually clarifies. However, the solubility in water is relatively low, only about [X] grams per 100 milliliters of water can be dissolved, which is due to the fact that there are many hydrophobic groups in the molecular structure, so the hydrophilicity is poor.
Its density is about [X] grams per cubic centimeter, which is similar to the density of common organic compounds. With this density, if it is placed in a specific liquid, its density can be roughly inferred according to the floating condition.
Furthermore, the stability of this substance is quite considerable. Under normal temperature and pressure and without the interference of special chemical reagents, it can be stored for a long time without significant chemical changes. However, it should be noted that it is more sensitive to light, high temperature and strong acid and base environments. When the light is too strong or the temperature is too high, it may cause changes in the molecular structure, causing changes in its physical properties and chemical activities. When exposed to strong acids and bases, it is prone to chemical reactions, which in turn destroy its original structure.
The above physical properties are of crucial significance in many fields such as chemical production and drug research and development, and can be used for separation, purification and application.
What are the chemical properties of 1-chloro-2-nitro-4- (trifluoromethyl) benzene?
1 + -Deuterium-2-amino-4- (triethylamino) benzene, this is an organic compound. Its chemical properties are quite complex, let me explain in detail for you.
First talk about its physical properties. Under normal conditions, or as a solid crystal, it has a certain melting point and boiling point. Its melting boiling point is affected by many factors such as intermolecular forces and hydrogen bonds. Those with strong intermolecular forces have relatively high melting boiling points; if hydrogen bonds can be formed within the molecule, it will also have a significant impact on the melting boiling point.
In terms of chemical activity, amino groups are groups with active properties. The nitrogen atom in the amino group has a solitary pair of electrons, which makes it easy to combine with protons and exhibit a certain alkalinity. This alkalinity allows the compound to accept protons in an acidic environment and generate corresponding salts. At the same time, the amino group can also participate in a variety of nucleophilic substitution reactions. For example, it can react with halogenated hydrocarbons. The solitary pair of electrons of the nitrogen atom attacks the carbon atom of the halogenated hydrocarbon, and the halogenated atom leaves, thus forming a new carbon-nitrogen bond and deriving other organic compounds. The triethylamino part of
also affects its chemical properties. This group is large in size and has a certain steric hindrance effect. Spatial steric hindrance will have an effect on the reaction process. In some reactions, due to the large triethylamino hindrance, the reaction reagent is difficult to approach the target reaction check point, resulting in a slow down of the reaction rate and even a change in the selectivity of the reaction.
Furthermore, the presence of the benzene ring endows the compound with special stability. The benzene ring has a conjugated large π bond, and the electron cloud is delocalized, which stabilizes the structure of the benzene ring. However, the benzene ring can also participate in the electrophilic substitution reaction. Because the amino group is an electron donor group, the electron cloud density of the benzene ring can increase, and it is more vulnerable to the attack of electrophilic reagents. Common electrophilic substitution reactions such as nitrification, halogenation, and sulfonation can occur on the benzene ring under
The substitution of deuterium atoms, although its chemical properties are similar to those of hydrogen atoms, will change the vibration frequency of related chemical bonds due to mass differences, which will affect the isotopic effect of reaction kinetics. In some reactions involving deuterium-carbon or deuterium-nitrogen bond cleavage, the reaction rate may be different from that of hydrogen-containing analogs.
Overall, 1 + -deuterium-2-amino-4- (triethylamino) benzene has rich and diverse chemical properties. It is influenced by the interaction of various groups in the molecule and the spatial structure. It may have important uses in organic synthesis and related fields.
First talk about its physical properties. Under normal conditions, or as a solid crystal, it has a certain melting point and boiling point. Its melting boiling point is affected by many factors such as intermolecular forces and hydrogen bonds. Those with strong intermolecular forces have relatively high melting boiling points; if hydrogen bonds can be formed within the molecule, it will also have a significant impact on the melting boiling point.
In terms of chemical activity, amino groups are groups with active properties. The nitrogen atom in the amino group has a solitary pair of electrons, which makes it easy to combine with protons and exhibit a certain alkalinity. This alkalinity allows the compound to accept protons in an acidic environment and generate corresponding salts. At the same time, the amino group can also participate in a variety of nucleophilic substitution reactions. For example, it can react with halogenated hydrocarbons. The solitary pair of electrons of the nitrogen atom attacks the carbon atom of the halogenated hydrocarbon, and the halogenated atom leaves, thus forming a new carbon-nitrogen bond and deriving other organic compounds. The triethylamino part of
also affects its chemical properties. This group is large in size and has a certain steric hindrance effect. Spatial steric hindrance will have an effect on the reaction process. In some reactions, due to the large triethylamino hindrance, the reaction reagent is difficult to approach the target reaction check point, resulting in a slow down of the reaction rate and even a change in the selectivity of the reaction.
Furthermore, the presence of the benzene ring endows the compound with special stability. The benzene ring has a conjugated large π bond, and the electron cloud is delocalized, which stabilizes the structure of the benzene ring. However, the benzene ring can also participate in the electrophilic substitution reaction. Because the amino group is an electron donor group, the electron cloud density of the benzene ring can increase, and it is more vulnerable to the attack of electrophilic reagents. Common electrophilic substitution reactions such as nitrification, halogenation, and sulfonation can occur on the benzene ring under
The substitution of deuterium atoms, although its chemical properties are similar to those of hydrogen atoms, will change the vibration frequency of related chemical bonds due to mass differences, which will affect the isotopic effect of reaction kinetics. In some reactions involving deuterium-carbon or deuterium-nitrogen bond cleavage, the reaction rate may be different from that of hydrogen-containing analogs.
Overall, 1 + -deuterium-2-amino-4- (triethylamino) benzene has rich and diverse chemical properties. It is influenced by the interaction of various groups in the molecule and the spatial structure. It may have important uses in organic synthesis and related fields.
What are the synthesis methods of 1-chloro-2-nitro-4- (trifluoromethyl) benzene?
The synthesis of 1-bromo-2-amino-4- (triethylamino) benzene is very important. This is your detailed description.
One method is to first take an appropriate benzene derivative, such as benzene containing a specific substituent, and use a brominating agent, such as liquid bromine or N-bromosuccinimide (NBS). Under suitable reaction conditions, if the catalyst exists and the temperature is controlled, the bromine atom can be introduced at a specific position in the benzene ring to obtain a benzene derivative containing bromine.
Then, the bromine-containing product is aminated with a suitable amination reagent, such as an ammonia derivative, in a suitable solvent or in the presence of an acid binding agent, so that the bromine atom is substituted with an amino group to obtain a compound containing bromine and an amino group.
As for the introduction of triethylamino, the above-mentioned product can be reacted with triethylamine under suitable reaction conditions, or in an alkaline environment. Through nucleophilic substitution reaction, the nitrogen atom in the triethylamine attacks the appropriate position on the benzene ring, thereby introducing triethylamino to obtain the target product 1-bromo-2-amino-4- (triethylamino) benzene.
There are other methods. The benzene ring can be aminated first, then brominated, and then triethylamino is introduced. However, it is necessary to pay attention to the control of the reaction conditions at each step to prevent side reactions from occurring. For example, during aminization, conditions such as temperature and reagent concentration will affect the selectivity and yield of the reaction. During the bromination process, it is also necessary to pay attention to the selectivity of the bromination position, which can be regulated by selecting appropriate catalysts, solvents and reaction temperatures. When triethylamino is introduced, factors such as alkalinity and reaction time also have a great influence on the reaction results. Fine operation is required to obtain products with higher yield and purity.
One method is to first take an appropriate benzene derivative, such as benzene containing a specific substituent, and use a brominating agent, such as liquid bromine or N-bromosuccinimide (NBS). Under suitable reaction conditions, if the catalyst exists and the temperature is controlled, the bromine atom can be introduced at a specific position in the benzene ring to obtain a benzene derivative containing bromine.
Then, the bromine-containing product is aminated with a suitable amination reagent, such as an ammonia derivative, in a suitable solvent or in the presence of an acid binding agent, so that the bromine atom is substituted with an amino group to obtain a compound containing bromine and an amino group.
As for the introduction of triethylamino, the above-mentioned product can be reacted with triethylamine under suitable reaction conditions, or in an alkaline environment. Through nucleophilic substitution reaction, the nitrogen atom in the triethylamine attacks the appropriate position on the benzene ring, thereby introducing triethylamino to obtain the target product 1-bromo-2-amino-4- (triethylamino) benzene.
There are other methods. The benzene ring can be aminated first, then brominated, and then triethylamino is introduced. However, it is necessary to pay attention to the control of the reaction conditions at each step to prevent side reactions from occurring. For example, during aminization, conditions such as temperature and reagent concentration will affect the selectivity and yield of the reaction. During the bromination process, it is also necessary to pay attention to the selectivity of the bromination position, which can be regulated by selecting appropriate catalysts, solvents and reaction temperatures. When triethylamino is introduced, factors such as alkalinity and reaction time also have a great influence on the reaction results. Fine operation is required to obtain products with higher yield and purity.
What are the precautions for storing and transporting 1-chloro-2-nitro-4- (trifluoromethyl) benzene?
1 + -Tritium-2-amino-4- (triethylamino) naphthalene, when storing and transporting, many matters need to be paid attention to.
Tritium is radioactive. When storing, a special container must be selected. This container must have excellent sealing to prevent tritium from escaping and causing environmental pollution and personal injury. And it needs to be placed in a specific place. The place should be far away from crowded places, with prominent warning signs, and special personnel to guard, monitor regularly, and record relevant data in detail.
Its transportation process should not be underestimated. The transportation vehicle must be specially modified and equipped with complete protective facilities to ensure smooth driving, shock absorption and turbulence, and avoid tritium leakage caused by accidental damage to the container. Transport personnel must be professionally trained and familiar with the characteristics, hazards and emergency treatment measures of tritium.
As for 2-amino-4- (triethylamino) naphthalene, due to its active chemical properties, storage should be protected from high temperatures, open flames and strong oxidants. It needs to be stored in a cool, dry and well-ventilated place to prevent moisture, oxidation and deterioration.
During transportation, it is also necessary to ensure that the packaging is in good condition to prevent collision and friction. When shipping with tritium, it is even more necessary to be careful and strictly zoned to avoid hazards caused by the interaction between the two. In short, for such special chemicals, all aspects of storage and transportation must be strictly treated, in accordance with relevant regulations and operating norms, to ensure personnel safety and environmental safety.
Tritium is radioactive. When storing, a special container must be selected. This container must have excellent sealing to prevent tritium from escaping and causing environmental pollution and personal injury. And it needs to be placed in a specific place. The place should be far away from crowded places, with prominent warning signs, and special personnel to guard, monitor regularly, and record relevant data in detail.
Its transportation process should not be underestimated. The transportation vehicle must be specially modified and equipped with complete protective facilities to ensure smooth driving, shock absorption and turbulence, and avoid tritium leakage caused by accidental damage to the container. Transport personnel must be professionally trained and familiar with the characteristics, hazards and emergency treatment measures of tritium.
As for 2-amino-4- (triethylamino) naphthalene, due to its active chemical properties, storage should be protected from high temperatures, open flames and strong oxidants. It needs to be stored in a cool, dry and well-ventilated place to prevent moisture, oxidation and deterioration.
During transportation, it is also necessary to ensure that the packaging is in good condition to prevent collision and friction. When shipping with tritium, it is even more necessary to be careful and strictly zoned to avoid hazards caused by the interaction between the two. In short, for such special chemicals, all aspects of storage and transportation must be strictly treated, in accordance with relevant regulations and operating norms, to ensure personnel safety and environmental safety.
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