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1-(Dichloromethyl)-4-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
965825 |
| Chemical Formula | C8H5Cl2F3 |
| Molar Mass | 225.026 g/mol |
| Appearance | Liquid (likely, based on similar compounds) |
| Boiling Point | Data needed |
| Melting Point | Data needed |
| Density | Data needed |
| Solubility In Water | Low (hydrophobic due to non - polar groups) |
| Vapor Pressure | Data needed |
| Flash Point | Data needed |
| Stability | Stable under normal conditions, but may react with strong oxidizing agents |
As an accredited 1-(Dichloromethyl)-4-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100 - gram bottles for 1-(dichloromethyl)-4-(trifluoromethyl)benzene packaging. |
| Storage | 1-(Dichloromethyl)-4-(trifluoromethyl)benzene should be stored in a cool, well - ventilated area away from heat, sparks, and open flames. Keep it in a tightly sealed container, preferably in a dedicated chemical storage cabinet. Avoid storing near oxidizing agents. Ensure the storage place is dry to prevent potential hydrolysis reactions. |
| Shipping | 1-(Dichloromethyl)-4-(trifluoromethyl)benzene is shipped in sealed, corrosion - resistant containers. Shipment adheres to strict chemical transportation regulations, ensuring safety during transit to prevent spills and environmental exposure. |
Competitive 1-(Dichloromethyl)-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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What are the main uses of 1- (dichloromethyl) -4- (trifluoromethyl) benzene?
1 - (dioxomethyl) -4 - (trioxomethyl) benzene, this compound has important uses in many fields.
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 series of reactions to build a molecular structure with specific pharmacological activities. For example, when developing new drugs for specific diseases, with its unique structure, it can be cleverly combined with the target target, and then exert therapeutic effects, or regulate specific physiological processes in the body, providing the possibility to overcome difficult diseases.
In the field of materials science, it also occupies a place. It can be used as an important raw material for synthesizing materials with special properties, giving materials unique properties. For example, when synthesizing polymer materials with excellent optical properties, the introduction of this compound can change the light absorption and emission characteristics of the material, making it suitable for optical display, optoelectronic devices and other fields, laying the foundation for improving material properties and expanding the application range.
In the field of organic synthetic chemistry, 1- (dioxomethyl) -4- (trioxomethyl) benzene is an important cornerstone. With its diverse reactivity check points, chemists can follow different reaction paths, modify and expand them, synthesize organic compounds with more complex structures and unique functions, and promote organic synthetic chemistry to new heights, providing strong support for exploring the relationship between structure and properties of novel compounds.
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 series of reactions to build a molecular structure with specific pharmacological activities. For example, when developing new drugs for specific diseases, with its unique structure, it can be cleverly combined with the target target, and then exert therapeutic effects, or regulate specific physiological processes in the body, providing the possibility to overcome difficult diseases.
In the field of materials science, it also occupies a place. It can be used as an important raw material for synthesizing materials with special properties, giving materials unique properties. For example, when synthesizing polymer materials with excellent optical properties, the introduction of this compound can change the light absorption and emission characteristics of the material, making it suitable for optical display, optoelectronic devices and other fields, laying the foundation for improving material properties and expanding the application range.
In the field of organic synthetic chemistry, 1- (dioxomethyl) -4- (trioxomethyl) benzene is an important cornerstone. With its diverse reactivity check points, chemists can follow different reaction paths, modify and expand them, synthesize organic compounds with more complex structures and unique functions, and promote organic synthetic chemistry to new heights, providing strong support for exploring the relationship between structure and properties of novel compounds.
What are the physical properties of 1- (dichloromethyl) -4- (trifluoromethyl) benzene?
1 - (dioxomethyl) -4 - (trifluoromethyl) benzene, which has unique physical properties. Its appearance is usually colorless to light yellow liquid, and it is often regarded as an important raw material and intermediate in the chemical industry.
Looking at its properties, it is liquid at room temperature and pressure, and can be miscible with many organic solvents such as ethanol and ether. This property gives it an advantage in the selection of solvents for organic synthesis reactions, which can effectively promote the full contact of the reactants and accelerate the reaction process.
The boiling point is about a certain temperature range, which is of great significance in the separation and purification process. By precisely controlling the temperature, it can effectively separate from other substances, thereby obtaining high-purity products.
The melting point also has a specific value. When the ambient temperature drops below the melting point, the substance will change from liquid to solid. This property needs to be taken into account during storage and transportation to ensure that the ambient temperature is suitable to prevent it from affecting the quality due to changes in state.
In addition, the density of this substance is different from that of water, which is crucial in some operations involving stratification and phase separation. Its activity in chemical reactions is closely related to the dioxomethyl and trifluoromethyl groups attached to the benzene ring. The strong electron-absorbing property of trifluoromethyl can change the electron cloud density of benzene ring, which in turn affects its chemical properties, causing it to exhibit different reactivity and selectivity from ordinary benzene derivatives in reactions such as electrophilic substitution.
Looking at its properties, it is liquid at room temperature and pressure, and can be miscible with many organic solvents such as ethanol and ether. This property gives it an advantage in the selection of solvents for organic synthesis reactions, which can effectively promote the full contact of the reactants and accelerate the reaction process.
The boiling point is about a certain temperature range, which is of great significance in the separation and purification process. By precisely controlling the temperature, it can effectively separate from other substances, thereby obtaining high-purity products.
The melting point also has a specific value. When the ambient temperature drops below the melting point, the substance will change from liquid to solid. This property needs to be taken into account during storage and transportation to ensure that the ambient temperature is suitable to prevent it from affecting the quality due to changes in state.
In addition, the density of this substance is different from that of water, which is crucial in some operations involving stratification and phase separation. Its activity in chemical reactions is closely related to the dioxomethyl and trifluoromethyl groups attached to the benzene ring. The strong electron-absorbing property of trifluoromethyl can change the electron cloud density of benzene ring, which in turn affects its chemical properties, causing it to exhibit different reactivity and selectivity from ordinary benzene derivatives in reactions such as electrophilic substitution.
Is 1- (dichloromethyl) -4- (trifluoromethyl) benzene chemically stable?
The chemical properties of 1 - (dimethyl) -4- (trimethyl) naphthalene are stable? To solve this question, we should analyze it in chemical terms.
The stability of organic compounds is related to their molecular structure. Dimethyl and trimethyl are based on the substitution position on the naphthalene ring. Methyl is a power supply group, which can affect the electron cloud density distribution of the naphthalene ring.
If dimethyl and trimethyl are at specific positions in the naphthalene ring, the electron cloud distribution of the molecule can tend to be uniform, forming the expansion of the conjugate system, or increasing its stability. If the methyl group is in the α-position of the naphthalene ring, it can form a superconjugate effect with the naphthalene ring, which can reduce the energy of the system and enhance the stability.
However, if the position of the substituent is improper, or the steric resistance increases. The volume of dimethyl and trimethyl groups is large. If they are close to each other and the space is crowded, the internal stress of the molecule will increase and the stability will decrease.
And the chemical reaction environment cannot be ignored. In the presence of high temperature, strong acid, strong base or strong oxidant, even if the structure is relatively stable 1- (dimethyl) -4- (trimethyl) naphthalene, reactions may occur, such as oxidation, substitution, etc., and the stability is difficult to survive.
In summary, the stability of 1- (dimethyl) -4- (trimethyl) naphthalene is uncertain. Structurally, the position of the substituent affects the electron cloud and spatial effects; in the environment, the reaction conditions can break its stable state. Therefore, it is necessary to comprehensively consider the structural and environmental factors to understand its stability.
The stability of organic compounds is related to their molecular structure. Dimethyl and trimethyl are based on the substitution position on the naphthalene ring. Methyl is a power supply group, which can affect the electron cloud density distribution of the naphthalene ring.
If dimethyl and trimethyl are at specific positions in the naphthalene ring, the electron cloud distribution of the molecule can tend to be uniform, forming the expansion of the conjugate system, or increasing its stability. If the methyl group is in the α-position of the naphthalene ring, it can form a superconjugate effect with the naphthalene ring, which can reduce the energy of the system and enhance the stability.
However, if the position of the substituent is improper, or the steric resistance increases. The volume of dimethyl and trimethyl groups is large. If they are close to each other and the space is crowded, the internal stress of the molecule will increase and the stability will decrease.
And the chemical reaction environment cannot be ignored. In the presence of high temperature, strong acid, strong base or strong oxidant, even if the structure is relatively stable 1- (dimethyl) -4- (trimethyl) naphthalene, reactions may occur, such as oxidation, substitution, etc., and the stability is difficult to survive.
In summary, the stability of 1- (dimethyl) -4- (trimethyl) naphthalene is uncertain. Structurally, the position of the substituent affects the electron cloud and spatial effects; in the environment, the reaction conditions can break its stable state. Therefore, it is necessary to comprehensively consider the structural and environmental factors to understand its stability.
What is the preparation method of 1- (dichloromethyl) -4- (trifluoromethyl) benzene?
To prepare 1 - (dioxomethyl) -4 - (trioxomethyl) benzene, the following method can be used.
First take an appropriate amount of benzene, use a specific catalyst and suitable reaction conditions, so that benzene and monohalomethane can be alkylated in a suitable solvent. This reaction requires fine regulation of temperature, pressure and the proportion of reactants, so that the reaction mainly generates p-halomethylbenzene.
Then, under the action of appropriate oxidants, such as selecting specific high-valent metal salts or strong oxidizing organic reagents, in a suitable reaction system, the halogenated methyl is gradually oxidized to dioxomethyl and trioxomethyl. This oxidation process is quite critical, and it is necessary to strictly control the amount of oxidant and the process of the reaction to avoid excessive oxidation or insufficient oxidation.
After each step of the reaction, suitable separation and purification methods, such as distillation, recrystallization, column chromatography, etc., are required to obtain high-purity intermediate products and final products. During the whole preparation process, factors such as the airtightness of the reaction device and the cleanliness of the reaction environment also have an important impact on the purity and yield of the product. In this way, after many careful operations and controls, it is expected to obtain the target product 1- (dioxy methyl) -4- (trioxy methyl) benzene.
First take an appropriate amount of benzene, use a specific catalyst and suitable reaction conditions, so that benzene and monohalomethane can be alkylated in a suitable solvent. This reaction requires fine regulation of temperature, pressure and the proportion of reactants, so that the reaction mainly generates p-halomethylbenzene.
Then, under the action of appropriate oxidants, such as selecting specific high-valent metal salts or strong oxidizing organic reagents, in a suitable reaction system, the halogenated methyl is gradually oxidized to dioxomethyl and trioxomethyl. This oxidation process is quite critical, and it is necessary to strictly control the amount of oxidant and the process of the reaction to avoid excessive oxidation or insufficient oxidation.
After each step of the reaction, suitable separation and purification methods, such as distillation, recrystallization, column chromatography, etc., are required to obtain high-purity intermediate products and final products. During the whole preparation process, factors such as the airtightness of the reaction device and the cleanliness of the reaction environment also have an important impact on the purity and yield of the product. In this way, after many careful operations and controls, it is expected to obtain the target product 1- (dioxy methyl) -4- (trioxy methyl) benzene.
What are the precautions for storing and transporting 1- (dichloromethyl) -4- (trifluoromethyl) benzene?
1 - (dioxomethyl) - 4 - (trioxomethyl) benzene requires attention to many matters during storage and transportation.
Its chemical properties are relatively special, and when storing, it should be placed in a cool, dry and well-ventilated place. This is because the substance may be sensitive to heat, and high temperature environments may cause chemical reactions, causing danger. If placed in a humid place, water vapor may react with the substance, changing its chemical structure and affecting quality. Good ventilation can disperse harmful gases that may evaporate in time and reduce safety risks.
Furthermore, keep away from fires and heat sources. This substance may be flammable, and it is easy to cause combustion or even explosion in case of open flames and hot topics. Therefore, smoking and fire are strictly prohibited in the storage area, and corresponding fire-fighting equipment should be equipped for emergencies.
The transportation process also needs to be cautious. Be sure to ensure that the packaging is complete and sealed. To prevent material leakage during transportation, not only pollute the environment, but also may cause harm to transporters and surrounding people. It is also crucial to choose the right means of transportation. According to its dangerous characteristics, follow the relevant transportation regulations, and select professional transportation personnel. During transportation, it is necessary to pay close attention to changes in environmental factors such as temperature and humidity, and take corresponding protective measures to ensure transportation safety. In short, the storage and transportation of chemicals such as 1- (dioxomethyl) -4- (trioxomethyl) benzene must be strictly followed and handled with caution to ensure the safety of personnel and the environment.
Its chemical properties are relatively special, and when storing, it should be placed in a cool, dry and well-ventilated place. This is because the substance may be sensitive to heat, and high temperature environments may cause chemical reactions, causing danger. If placed in a humid place, water vapor may react with the substance, changing its chemical structure and affecting quality. Good ventilation can disperse harmful gases that may evaporate in time and reduce safety risks.
Furthermore, keep away from fires and heat sources. This substance may be flammable, and it is easy to cause combustion or even explosion in case of open flames and hot topics. Therefore, smoking and fire are strictly prohibited in the storage area, and corresponding fire-fighting equipment should be equipped for emergencies.
The transportation process also needs to be cautious. Be sure to ensure that the packaging is complete and sealed. To prevent material leakage during transportation, not only pollute the environment, but also may cause harm to transporters and surrounding people. It is also crucial to choose the right means of transportation. According to its dangerous characteristics, follow the relevant transportation regulations, and select professional transportation personnel. During transportation, it is necessary to pay close attention to changes in environmental factors such as temperature and humidity, and take corresponding protective measures to ensure transportation safety. In short, the storage and transportation of chemicals such as 1- (dioxomethyl) -4- (trioxomethyl) benzene must be strictly followed and handled with caution to ensure the safety of personnel and the environment.
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