Linshang Chemical
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Benzene, 1,5-Dichloro-2-Methyl-4-(Trifluoromethyl)-
Linshang Chemical
|
HS Code |
562069 |
| Chemical Formula | C7H5Cl2F3 |
| Molar Mass | 215.015 g/mol |
| Appearance | Unknown (depends on purity and state) |
| Solubility In Water | Low (organic compound, likely hydrophobic) |
| Odor | Unknown, no common data |
As an accredited Benzene, 1,5-Dichloro-2-Methyl-4-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1,5 - dichloro - 2 - methyl - 4 - (trifluoromethyl)benzene in sealed chemical - grade bottle. |
| Storage | 1,5 - Dichloro - 2 - methyl - 4 - (trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area away from heat sources and ignition sources. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents, reducing agents, and reactive chemicals to prevent dangerous reactions. |
| Shipping | 1,5 - Dichloro - 2 - methyl - 4 - (trifluoromethyl) benzene is a chemical. It should be shipped in well - sealed, corrosion - resistant containers, following all hazardous chemical shipping regulations to ensure safety during transit. |
Competitive Benzene, 1,5-Dichloro-2-Methyl-4-(Trifluoromethyl)- prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615365006308
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What is the main use of this product 1,5-dichloro-2-methyl-4- (trifluoromethyl) benzene?
The name of this drug is 1,5-dioxy-2-methyl-4- (triethoxymethyl) furan, and its main use is quite critical.
In the field of medicine, this drug has unique effects. It can be used as a key intermediate to help synthesize many specific drugs. For example, some new drugs developed for specific diseases, 1,5-dioxy-2-methyl-4- (triethoxymethyl) furan, in its synthesis process, acts as an indispensable raw material. Through fine chemical reactions, it shapes the active structure of the drug and provides strong support for the treatment of diseases.
In the chemical industry, it is also an important member. Can participate in the preparation of high value-added organic compounds. Due to its special chemical structure, it can react with a variety of chemical substances to generate chemical products with special properties, such as polymer materials with special properties, or functional additives for specific environments, which play an important role in material modification and performance optimization, expand the application scope of chemical products, and improve product quality and performance.
At the level of scientific research and exploration, this compound is used as a research object to provide an opportunity for chemical synthesis methodology and reaction mechanism exploration. By studying its reaction characteristics and structural changes, researchers can deeply understand the relevant chemical reaction laws, lay a theoretical foundation for the development of new chemical synthesis paths and new catalysts, and promote the progress and development of cutting-edge fields of chemical science.
In the field of medicine, this drug has unique effects. It can be used as a key intermediate to help synthesize many specific drugs. For example, some new drugs developed for specific diseases, 1,5-dioxy-2-methyl-4- (triethoxymethyl) furan, in its synthesis process, acts as an indispensable raw material. Through fine chemical reactions, it shapes the active structure of the drug and provides strong support for the treatment of diseases.
In the chemical industry, it is also an important member. Can participate in the preparation of high value-added organic compounds. Due to its special chemical structure, it can react with a variety of chemical substances to generate chemical products with special properties, such as polymer materials with special properties, or functional additives for specific environments, which play an important role in material modification and performance optimization, expand the application scope of chemical products, and improve product quality and performance.
At the level of scientific research and exploration, this compound is used as a research object to provide an opportunity for chemical synthesis methodology and reaction mechanism exploration. By studying its reaction characteristics and structural changes, researchers can deeply understand the relevant chemical reaction laws, lay a theoretical foundation for the development of new chemical synthesis paths and new catalysts, and promote the progress and development of cutting-edge fields of chemical science.
What are the physical properties of 1,5-dichloro-2-methyl-4- (trifluoromethyl) benzene
1% 2C5-dioxy-2-methyl-4- (triethylmethyl) naphthalene is a special organic compound whose physical properties are worthy of investigation.
Looking at its morphology, at room temperature, this substance is mostly solid, similar to coagulation, with a fine and solid texture. Its color may be colorless and transparent, or slightly yellowish, and when pure, it is as clear as ice crystals.
When it comes to the melting point, due to the special interaction of dioxy, methyl and triethylmethyl in its molecular structure, it has a high melting point and requires considerable heat to convert it from a solid state to a liquid state. When placed in a high temperature environment, at a specific temperature, it begins to melt into a flowing liquid. The boiling point is also not low, and a large amount of heat energy needs to be given to make it boil and vaporize. This property makes the compound stable in general environments, and it is not easy to change the state easily due to temperature fluctuations.
In addition to solubility, this compound has good solubility in organic solvents. Common organic solvents such as ethanol and ether can form a certain force between their molecules to cause it to dissolve. However, the solubility in water is extremely low, because its molecular polarity is quite different from that of water, it is difficult for water to destroy the intermolecular force of the compound and disperse it.
In addition, its density is slightly larger than that of water, and if it is placed in water, it will sink to the bottom. Its refractive index also has a unique value. When light passes through the substance, the direction of propagation changes differently from that of common substances. This property may be of potential value in optics-related applications.
In summary, the physical properties of 1% 2C5-dioxy-2-methyl-4- (triethylmethyl) naphthalene are determined by its unique molecular structure, and may have unusual uses and significance in many fields.
Looking at its morphology, at room temperature, this substance is mostly solid, similar to coagulation, with a fine and solid texture. Its color may be colorless and transparent, or slightly yellowish, and when pure, it is as clear as ice crystals.
When it comes to the melting point, due to the special interaction of dioxy, methyl and triethylmethyl in its molecular structure, it has a high melting point and requires considerable heat to convert it from a solid state to a liquid state. When placed in a high temperature environment, at a specific temperature, it begins to melt into a flowing liquid. The boiling point is also not low, and a large amount of heat energy needs to be given to make it boil and vaporize. This property makes the compound stable in general environments, and it is not easy to change the state easily due to temperature fluctuations.
In addition to solubility, this compound has good solubility in organic solvents. Common organic solvents such as ethanol and ether can form a certain force between their molecules to cause it to dissolve. However, the solubility in water is extremely low, because its molecular polarity is quite different from that of water, it is difficult for water to destroy the intermolecular force of the compound and disperse it.
In addition, its density is slightly larger than that of water, and if it is placed in water, it will sink to the bottom. Its refractive index also has a unique value. When light passes through the substance, the direction of propagation changes differently from that of common substances. This property may be of potential value in optics-related applications.
In summary, the physical properties of 1% 2C5-dioxy-2-methyl-4- (triethylmethyl) naphthalene are determined by its unique molecular structure, and may have unusual uses and significance in many fields.
Is 1,5-dichloro-2-methyl-4 - (trifluoromethyl) benzene chemically stable?
The chemical properties of 1% 2C5-dioxy-2-methyl-4- (trichloromethyl) quinine are relatively stable. This compound has a certain stability due to the special arrangement of atoms and chemical bonds in the molecular structure.
From its structure, the dioxy group is relatively stable and plays a certain role in stabilizing the whole molecule. The existence of methyl groups, because of its saturated alkyl group, is relatively inert in chemical properties, generally not easy to react, which helps to stabilize the molecular framework. The trichloromethyl part, although the chlorine atom has a large electronegativity and strong electron absorption ability, interacts with surrounding groups in this specific molecular environment, and the overall structure is not overly active.
In common chemical environments, the compound will not easily decompose or react violently. Under normal temperature and pressure, it can maintain a relatively stable state and can withstand a certain degree of environmental changes such as temperature and humidity without changing its chemical structure. However, under some extreme conditions, such as high temperature, strong oxidants or the presence of specific catalysts, its stability will be challenged, which may trigger certain chemical reactions and change its chemical structure and properties.
Overall, under conventional conditions, the chemical properties of 1% 2C5-dioxy-2-methyl-4- (trichloromethyl) quinine are relatively stable, but under special conditions, the stability will be affected.
From its structure, the dioxy group is relatively stable and plays a certain role in stabilizing the whole molecule. The existence of methyl groups, because of its saturated alkyl group, is relatively inert in chemical properties, generally not easy to react, which helps to stabilize the molecular framework. The trichloromethyl part, although the chlorine atom has a large electronegativity and strong electron absorption ability, interacts with surrounding groups in this specific molecular environment, and the overall structure is not overly active.
In common chemical environments, the compound will not easily decompose or react violently. Under normal temperature and pressure, it can maintain a relatively stable state and can withstand a certain degree of environmental changes such as temperature and humidity without changing its chemical structure. However, under some extreme conditions, such as high temperature, strong oxidants or the presence of specific catalysts, its stability will be challenged, which may trigger certain chemical reactions and change its chemical structure and properties.
Overall, under conventional conditions, the chemical properties of 1% 2C5-dioxy-2-methyl-4- (trichloromethyl) quinine are relatively stable, but under special conditions, the stability will be affected.
What is the production process of 1,5-dichloro-2-methyl-4- (trifluoromethyl) benzene?
The preparation process of 1% 2C5-dioxo-2-methyl-4- (triethylmethyl) naphthalene is particularly exquisite. The method first takes an appropriate amount of naphthalene as the base, and the stability and reactivity of its aromatic ring are used to lay the basis for the reaction.
First, a specific methylation reagent is mixed with naphthalene, and the methylation reaction is carried out at a suitable temperature and catalyst environment. This step aims to introduce methyl at a specific position of the naphthalene ring. The temperature needs to be precisely controlled. If the cap temperature is too high or the side reaction of polymethylation is caused, if it is too low, the reaction will be delayed. The catalyst used also needs to be carefully selected to ensure that its activity is moderate, which can not only promote the reaction speed, but also not cause too many by-products
The introduction of a dioxy group is often used as a reagent with a dioxy structure to react with methylated naphthalene derivatives under alkali catalysis. This process requires attention to the amount of base and the reaction time. Too much or too little base affects the location and efficiency of dioxy group access; if the time is too short, the reaction will not be completed, and if it is too long, the product will decompose or overreact.
As for the introduction of triethyl methyl, it is a more critical step. Halogenated hydrocarbons containing triethyl are often used, and in the presence of metal catalysts and ligands, the coupling reaction occurs with the previous product. This step requires a high degree of anhydrous and oxygen-free reaction system. A small amount of water or oxygen can deactivate the metal catalyst and cause the reaction to fail. At the same time, the choice of ligands also depends on the selectivity and yield of the reaction, which needs to be carefully selected according to the structural characteristics of the substrate.
After the reaction is completed, the product is separated and purified in multiple steps. First, the method of extraction is used to separate the organic phase and the aqueous phase to remove a large number of water-soluble impurities; followed by column chromatography, according to the polarity of the product and the impurity, the separation is achieved on the silica gel column, and the final pure 1% 2C5-dioxy-2-methyl-4 - (triethylmethyl) naphthalene is obtained. The entire preparation process is interconnected, and each step needs to be carefully controlled to obtain the ideal product.
First, a specific methylation reagent is mixed with naphthalene, and the methylation reaction is carried out at a suitable temperature and catalyst environment. This step aims to introduce methyl at a specific position of the naphthalene ring. The temperature needs to be precisely controlled. If the cap temperature is too high or the side reaction of polymethylation is caused, if it is too low, the reaction will be delayed. The catalyst used also needs to be carefully selected to ensure that its activity is moderate, which can not only promote the reaction speed, but also not cause too many by-products
The introduction of a dioxy group is often used as a reagent with a dioxy structure to react with methylated naphthalene derivatives under alkali catalysis. This process requires attention to the amount of base and the reaction time. Too much or too little base affects the location and efficiency of dioxy group access; if the time is too short, the reaction will not be completed, and if it is too long, the product will decompose or overreact.
As for the introduction of triethyl methyl, it is a more critical step. Halogenated hydrocarbons containing triethyl are often used, and in the presence of metal catalysts and ligands, the coupling reaction occurs with the previous product. This step requires a high degree of anhydrous and oxygen-free reaction system. A small amount of water or oxygen can deactivate the metal catalyst and cause the reaction to fail. At the same time, the choice of ligands also depends on the selectivity and yield of the reaction, which needs to be carefully selected according to the structural characteristics of the substrate.
After the reaction is completed, the product is separated and purified in multiple steps. First, the method of extraction is used to separate the organic phase and the aqueous phase to remove a large number of water-soluble impurities; followed by column chromatography, according to the polarity of the product and the impurity, the separation is achieved on the silica gel column, and the final pure 1% 2C5-dioxy-2-methyl-4 - (triethylmethyl) naphthalene is obtained. The entire preparation process is interconnected, and each step needs to be carefully controlled to obtain the ideal product.
What are the precautions for the use of 1,5-dichloro-2-methyl-4- (trifluoromethyl) benzene?
1% 2C5-dioxy-2-methyl-4- (trifluoromethyl) pyridine is a highly toxic chemical. When using it, many things must be paid attention to.
First protection. Users must wear comprehensive protective clothing, such as protective clothing and protective gloves, to prevent skin contact. Because of its toxicity, a little contamination may endanger health and cause skin burns, allergies and other diseases. Facial protection is also indispensable. Wear a gas mask to ensure that the air you breathe is clean and free. Avoid inhaling the steam and smoke of this poison, otherwise it is easy to cause respiratory damage or even more serious health problems.
Times and operation. The operation should be carried out in a well-ventilated place, preferably in a fume hood. Good ventilation can quickly disperse volatile toxic gases, reduce the concentration of poisons in the air, and reduce the risk of poisoning in the group. When taking it, the method must be precise and meticulous to prevent it from leaking. If there is a leak, it should be properly disposed of immediately according to professional procedures. It must not be taken lightly to avoid the spread of poisons and cause greater harm.
The other is storage. It needs to be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Due to its chemical nature or relatively active, high temperature and open flame may cause dangerous reactions. At the same time, it should be stored separately from oxidants, acids, alkalis, etc., and must not be mixed to prevent severe chemical reactions from occurring, resulting in explosions, leaks and other serious accidents.
In addition, the place of use should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. In the event of an emergency, it can be responded to in time. Those involved in the use must undergo professional training and be familiar with its dangerous characteristics, safety operating procedures and emergency disposal methods before they can operate.
First protection. Users must wear comprehensive protective clothing, such as protective clothing and protective gloves, to prevent skin contact. Because of its toxicity, a little contamination may endanger health and cause skin burns, allergies and other diseases. Facial protection is also indispensable. Wear a gas mask to ensure that the air you breathe is clean and free. Avoid inhaling the steam and smoke of this poison, otherwise it is easy to cause respiratory damage or even more serious health problems.
Times and operation. The operation should be carried out in a well-ventilated place, preferably in a fume hood. Good ventilation can quickly disperse volatile toxic gases, reduce the concentration of poisons in the air, and reduce the risk of poisoning in the group. When taking it, the method must be precise and meticulous to prevent it from leaking. If there is a leak, it should be properly disposed of immediately according to professional procedures. It must not be taken lightly to avoid the spread of poisons and cause greater harm.
The other is storage. It needs to be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Due to its chemical nature or relatively active, high temperature and open flame may cause dangerous reactions. At the same time, it should be stored separately from oxidants, acids, alkalis, etc., and must not be mixed to prevent severe chemical reactions from occurring, resulting in explosions, leaks and other serious accidents.
In addition, the place of use should be equipped with the corresponding variety and quantity of fire fighting equipment and leakage emergency treatment equipment. In the event of an emergency, it can be responded to in time. Those involved in the use must undergo professional training and be familiar with its dangerous characteristics, safety operating procedures and emergency disposal methods before they can operate.
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