Linshang Chemical
PRODUCTS
Benzene, 1-Chloro-4-(Chloromethyl)-2-(Trifluoromethyl)-
Linshang Chemical
|
HS Code |
778341 |
| Chemical Formula | C8H5Cl2F3 |
| Molecular Weight | 227.025 |
As an accredited Benzene, 1-Chloro-4-(Chloromethyl)-2-(Trifluoromethyl)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram vial packaging for 1 - chloro - 4 - (chloromethyl)-2-(trifluoromethyl)benzene. |
| Storage | **Storage of 1 - chloro - 4 - (chloromethyl)-2-(trifluoromethyl)benzene**: Store this chemical in a cool, dry, well - ventilated area, away from heat sources and open flames. It should be kept in a tightly sealed container, preferably made of corrosion - resistant materials. Isolate it from oxidizing agents, reducing agents, and reactive chemicals to prevent potential reactions. Ensure proper labeling for easy identification and handling. |
| Shipping | 1 - Chloro - 4 - (chloromethyl)-2-(trifluoromethyl)benzene is shipped in accordance with strict chemical transport regulations. Packed in specialized, sealed containers to prevent leakage, transported by carriers trained in handling hazardous chemicals. |
Competitive Benzene, 1-Chloro-4-(Chloromethyl)-2-(Trifluoromethyl)- 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 Benzene, 1-Chloro-4-(Chloromethyl)-2-(Trifluoromethyl)- in China?
As a trusted Benzene, 1-Chloro-4-(Chloromethyl)-2-(Trifluoromethyl)- manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
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 Benzene, 1-Chloro-4-(Chloromethyl)-2-(Trifluoromethyl)- 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 physical properties of 1-chloro-4- (chloromethyl) -2- (trifluoromethyl) benzene?
1 + -Deuterium-4- (deuterium methyl) -2- (trideuterium methyl) benzene, the physical properties of this substance are as follows:
Its appearance may be a colorless and transparent liquid, because most of these organic compounds are liquid at room temperature and pressure. It has a specific odor, but the specific odor varies depending on the structure and functional group. This compound may have an aromatic odor. Due to its benzene ring structure, many organic compounds containing benzene rings have a unique aromatic smell.
In terms of boiling point, due to the introduction of deuterium atoms into the molecule, the mass of deuterium atoms is greater than that of hydrogen atoms, resulting in a change in the intermolecular force. Compared with similar compounds containing ordinary hydrogen atoms, its boiling point may be increased. However, the exact boiling point needs to be accurately determined by experiments, and it can be speculated that it is higher than the simple alkyl derivatives of ordinary benzene.
The melting point is also affected by deuterium atoms, and the melting point may also increase due to the increase in molecular weight and the change of intermolecular forces. Its density is greater than that of water, because the weight of deuterium atoms increases the overall molecular weight, and the mass is greater under the same volume, so the density is greater than that of water.
In terms of solubility, because it is an organic compound with a benzene ring hydrophobic structure, its solubility in water is extremely low, and it is soluble in common organic solvents, such as ether, dichloromethane, chloroform, etc. Due to the principle of "similarity and compatibility", the structure and polarity of organic compounds are similar, so they dissolve each other.
In addition, the deuterium atoms in this compound give it a unique signal in NMR spectroscopy, which can help researchers accurately identify and analyze its structure. This is because the spin characteristics of deuterium atoms are different from those of hydrogen atoms, and they exhibit unique chemical shifts and coupling constants in the spectrum.
Its appearance may be a colorless and transparent liquid, because most of these organic compounds are liquid at room temperature and pressure. It has a specific odor, but the specific odor varies depending on the structure and functional group. This compound may have an aromatic odor. Due to its benzene ring structure, many organic compounds containing benzene rings have a unique aromatic smell.
In terms of boiling point, due to the introduction of deuterium atoms into the molecule, the mass of deuterium atoms is greater than that of hydrogen atoms, resulting in a change in the intermolecular force. Compared with similar compounds containing ordinary hydrogen atoms, its boiling point may be increased. However, the exact boiling point needs to be accurately determined by experiments, and it can be speculated that it is higher than the simple alkyl derivatives of ordinary benzene.
The melting point is also affected by deuterium atoms, and the melting point may also increase due to the increase in molecular weight and the change of intermolecular forces. Its density is greater than that of water, because the weight of deuterium atoms increases the overall molecular weight, and the mass is greater under the same volume, so the density is greater than that of water.
In terms of solubility, because it is an organic compound with a benzene ring hydrophobic structure, its solubility in water is extremely low, and it is soluble in common organic solvents, such as ether, dichloromethane, chloroform, etc. Due to the principle of "similarity and compatibility", the structure and polarity of organic compounds are similar, so they dissolve each other.
In addition, the deuterium atoms in this compound give it a unique signal in NMR spectroscopy, which can help researchers accurately identify and analyze its structure. This is because the spin characteristics of deuterium atoms are different from those of hydrogen atoms, and they exhibit unique chemical shifts and coupling constants in the spectrum.
What are the chemical properties of 1-chloro-4- (chloromethyl) -2- (trifluoromethyl) benzene
1 + - + chlorine - 4 - (chloromethyl) - 2 - (trichloromethyl) benzene is an organic compound with unique properties. In ancient Chinese,
This compound has a colorless to light yellow liquid appearance and a specific odor. It has a certain solubility. It is quite soluble in organic solvents such as ethanol and ether, but it is difficult to dissolve in water. Because its structure is mostly based on hydrocarbons, it is different from the polarity of water.
In terms of chemical activity, the chlorine atoms in its molecules are very active. The chloromethyl and trichloromethyl groups attached to the benzene ring are the activity check points of the reaction. When encountering nucleophiles, chlorine atoms are easily replaced by nucleophiles. For example, if co-heated with an aqueous solution of sodium hydroxide, chlorine atoms can be replaced by hydroxyl groups to form corresponding alcohols.
And because its structure contains many chlorine atoms, it has considerable stability and flame retardant properties. In high temperature environments, chlorine atoms in molecules can play a role in inhibiting the process of combustion.
Its chemical activity is also reflected in its participation in many organic synthesis reactions. It can further derive a variety of organic compounds with different functions through halogenation reactions, substitution reactions, etc., which are of great use in the field of organic synthesis. Due to its unique chemical properties, it has broad application prospects in materials science, medicinal chemistry, and many other fields.
This compound has a colorless to light yellow liquid appearance and a specific odor. It has a certain solubility. It is quite soluble in organic solvents such as ethanol and ether, but it is difficult to dissolve in water. Because its structure is mostly based on hydrocarbons, it is different from the polarity of water.
In terms of chemical activity, the chlorine atoms in its molecules are very active. The chloromethyl and trichloromethyl groups attached to the benzene ring are the activity check points of the reaction. When encountering nucleophiles, chlorine atoms are easily replaced by nucleophiles. For example, if co-heated with an aqueous solution of sodium hydroxide, chlorine atoms can be replaced by hydroxyl groups to form corresponding alcohols.
And because its structure contains many chlorine atoms, it has considerable stability and flame retardant properties. In high temperature environments, chlorine atoms in molecules can play a role in inhibiting the process of combustion.
Its chemical activity is also reflected in its participation in many organic synthesis reactions. It can further derive a variety of organic compounds with different functions through halogenation reactions, substitution reactions, etc., which are of great use in the field of organic synthesis. Due to its unique chemical properties, it has broad application prospects in materials science, medicinal chemistry, and many other fields.
What are the main uses of 1-chloro-4- (chloromethyl) -2- (trifluoromethyl) benzene?
1 + - -4- (methyl) -2- (triethyl) silicon, which is mostly used in pill formulas and equipment repair.
In pill formulas, this can be combined with, so that the power of can be destroyed, and it has a miraculous effect. For example, "Origin Gathering Pill", this pill can consolidate the essence and improve the essence of the practitioner. Then the properties are different, so as to blend, and 1 + - -4- (methyl) -2- (triethyl) silicon is added to it, which can be used as a clever medium, and the properties are mutual, and the phase is formed, and the pills produced are better and more effective.
In equipment repair, it also has extraordinary uses. If you create a "green light", it will take thousands of years, and the material fusion is very important. 1 + - -4- (methyl) -2- (triethyl) silicon is integrated into the building material, which can increase the fit of the material, make the body more efficient and profitable. And the characteristics of this silicon can form a barrier to the body, resist external force intrusion, improve the performance of the body, make it easier for the mind of the holder to communicate, and get the heart and hand of the dance, and create a power beyond the usual. In addition, regardless of pill formula or equipment repair, 1 + - -4- (methyl) -2- (triethyl) silicon is an indispensable precious material. Its use is extensive, its effect is amazing, and its status in the repair world is very important.
In pill formulas, this can be combined with, so that the power of can be destroyed, and it has a miraculous effect. For example, "Origin Gathering Pill", this pill can consolidate the essence and improve the essence of the practitioner. Then the properties are different, so as to blend, and 1 + - -4- (methyl) -2- (triethyl) silicon is added to it, which can be used as a clever medium, and the properties are mutual, and the phase is formed, and the pills produced are better and more effective.
In equipment repair, it also has extraordinary uses. If you create a "green light", it will take thousands of years, and the material fusion is very important. 1 + - -4- (methyl) -2- (triethyl) silicon is integrated into the building material, which can increase the fit of the material, make the body more efficient and profitable. And the characteristics of this silicon can form a barrier to the body, resist external force intrusion, improve the performance of the body, make it easier for the mind of the holder to communicate, and get the heart and hand of the dance, and create a power beyond the usual. In addition, regardless of pill formula or equipment repair, 1 + - -4- (methyl) -2- (triethyl) silicon is an indispensable precious material. Its use is extensive, its effect is amazing, and its status in the repair world is very important.
What are the synthesis methods of 1-chloro-4- (chloromethyl) -2- (trifluoromethyl) benzene?
To prepare 1-bromo-4- (bromomethyl) -2- (trifluoromethyl) benzene, it can be obtained from the common organic synthesis method.
First, the benzene derivative containing the corresponding substituent is used as the starting material. First, the benzene containing trifluoromethyl can be obtained by electrophilic substitution reaction, so that trifluoromethyl can be introduced into the benzene ring. For example, starting with benzene, with trifluoromethylation reagents such as trifluoromethylhalide magnesium, etc., under the action of suitable catalysts such as palladium catalysts, benzene containing trifluoromethyl can be obtained.
Then, on this product, a halogenation reaction is used to introduce bromine atoms at specific positions in the benzene ring. A suitable halogenated reagent, such as bromine, can be selected under the catalysis of iron powder or iron tribromide to position the bromine atom at a specific position. Attention should be paid to the regulation of reaction conditions to achieve the required substitution position selectivity.
As for the introduction of bromomethyl, the benzene derivative containing trifluoromethyl and bromine can be reacted with formaldehyde and hydrogen chloride gas under the action of a specific catalyst to undergo chloromethylation to obtain the product containing chloromethyl. After that, a brominating reagent such as sodium bromide is used to exchange halogen with the product containing chloromethyl to convert the chloromethyl to bromomethyl, thereby obtaining the target product 1-bromo-4- (bromomethyl) -2 - (trifluoromethyl) benzene.
Second, the method of gradually constructing the benzene ring can also be used. First, an appropriate small organic molecule, such as an olefin containing trifluoromethyl, and an olefin containing bromine and a substituent that can be subsequently converted into bromomethyl, is used to construct the benzene ring structure through cyclization reaction. For example, by using cyclization reactions such as Diels-Alder reaction, the diene body reacts with the diene body to form a benzene ring skeleton. Then, the substituents on the formed benzene ring are modified and converted, and the substituents are gradually converted into the target bromine and bromomethyl through a series of reactions such as oxidation, reduction, and substitution, and finally the target compound can be obtained. During the synthesis process, each step of the reaction requires precise control of reaction conditions, such as temperature, pressure, and catalyst dosage, to ensure the smooth progress of the reaction and the purity and yield of the product.
First, the benzene derivative containing the corresponding substituent is used as the starting material. First, the benzene containing trifluoromethyl can be obtained by electrophilic substitution reaction, so that trifluoromethyl can be introduced into the benzene ring. For example, starting with benzene, with trifluoromethylation reagents such as trifluoromethylhalide magnesium, etc., under the action of suitable catalysts such as palladium catalysts, benzene containing trifluoromethyl can be obtained.
Then, on this product, a halogenation reaction is used to introduce bromine atoms at specific positions in the benzene ring. A suitable halogenated reagent, such as bromine, can be selected under the catalysis of iron powder or iron tribromide to position the bromine atom at a specific position. Attention should be paid to the regulation of reaction conditions to achieve the required substitution position selectivity.
As for the introduction of bromomethyl, the benzene derivative containing trifluoromethyl and bromine can be reacted with formaldehyde and hydrogen chloride gas under the action of a specific catalyst to undergo chloromethylation to obtain the product containing chloromethyl. After that, a brominating reagent such as sodium bromide is used to exchange halogen with the product containing chloromethyl to convert the chloromethyl to bromomethyl, thereby obtaining the target product 1-bromo-4- (bromomethyl) -2 - (trifluoromethyl) benzene.
Second, the method of gradually constructing the benzene ring can also be used. First, an appropriate small organic molecule, such as an olefin containing trifluoromethyl, and an olefin containing bromine and a substituent that can be subsequently converted into bromomethyl, is used to construct the benzene ring structure through cyclization reaction. For example, by using cyclization reactions such as Diels-Alder reaction, the diene body reacts with the diene body to form a benzene ring skeleton. Then, the substituents on the formed benzene ring are modified and converted, and the substituents are gradually converted into the target bromine and bromomethyl through a series of reactions such as oxidation, reduction, and substitution, and finally the target compound can be obtained. During the synthesis process, each step of the reaction requires precise control of reaction conditions, such as temperature, pressure, and catalyst dosage, to ensure the smooth progress of the reaction and the purity and yield of the product.
What are the precautions for using 1-chloro-4- (chloromethyl) -2- (trifluoromethyl) benzene?
1 + -Alkane-4- (alkyl) -2- (triethyl alkyl) ether is an organic compound. During use, the following things should be paid attention to:
First, this compound has a certain volatility. When used in poorly ventilated areas, its volatile gaseous substances or accumulation not only irritate the user's respiratory organs, but also cause dizziness, nausea and other discomforts. Therefore, when using it, make sure that the place is well ventilated. Natural ventilation or mechanical ventilation can be used to fully circulate the air, disperse the volatile gas, and ensure the safety of the working environment.
Second, its chemical properties may be unstable under specific conditions. In case of open flame or hot topic, there is a risk of causing combustion and explosion. Therefore, during use, be sure to keep away from fire and heat sources. Open flame operations such as welding and cutting should be strictly prohibited in the vicinity. At the same time, explosion-proof electrical equipment is also selected to prevent the generated electric sparks from igniting the object.
Third, this compound may have irritating effects on the skin and eyes. When operating, when taking personal protective measures, such as wearing protective gloves, choose chemical-resistant rubber gloves to block their contact with the skin; wearing protective glasses can effectively prevent them from splashing into the eyes. If you accidentally contact, you should immediately rinse with plenty of water and seek medical treatment if necessary.
Fourth, storage should not be ignored. It should be placed in a cool, dry and ventilated place, away from oxidants, acids and other substances. Because of its chemical reaction with these substances, it can cause dangerous conditions. Storage containers should also be well sealed to prevent leakage. And obvious warning signs should be posted to remind others of its danger.
Fifth, the use of personnel should be professionally trained and familiar with its nature, use methods and emergency measures. In the event of an accident such as leakage, it can respond quickly and correctly to reduce the harm. In the event of a small amount of leakage, it can be absorbed by inert materials such as sand and vermiculite; in the event of a large amount of leakage, personnel should be evacuated immediately, the scene should be sealed, and the police should be called for assistance.
First, this compound has a certain volatility. When used in poorly ventilated areas, its volatile gaseous substances or accumulation not only irritate the user's respiratory organs, but also cause dizziness, nausea and other discomforts. Therefore, when using it, make sure that the place is well ventilated. Natural ventilation or mechanical ventilation can be used to fully circulate the air, disperse the volatile gas, and ensure the safety of the working environment.
Second, its chemical properties may be unstable under specific conditions. In case of open flame or hot topic, there is a risk of causing combustion and explosion. Therefore, during use, be sure to keep away from fire and heat sources. Open flame operations such as welding and cutting should be strictly prohibited in the vicinity. At the same time, explosion-proof electrical equipment is also selected to prevent the generated electric sparks from igniting the object.
Third, this compound may have irritating effects on the skin and eyes. When operating, when taking personal protective measures, such as wearing protective gloves, choose chemical-resistant rubber gloves to block their contact with the skin; wearing protective glasses can effectively prevent them from splashing into the eyes. If you accidentally contact, you should immediately rinse with plenty of water and seek medical treatment if necessary.
Fourth, storage should not be ignored. It should be placed in a cool, dry and ventilated place, away from oxidants, acids and other substances. Because of its chemical reaction with these substances, it can cause dangerous conditions. Storage containers should also be well sealed to prevent leakage. And obvious warning signs should be posted to remind others of its danger.
Fifth, the use of personnel should be professionally trained and familiar with its nature, use methods and emergency measures. In the event of an accident such as leakage, it can respond quickly and correctly to reduce the harm. In the event of a small amount of leakage, it can be absorbed by inert materials such as sand and vermiculite; in the event of a large amount of leakage, personnel should be evacuated immediately, the scene should be sealed, and the police should be called for assistance.
Scan to WhatsApp
