Linshang Chemical
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1-(Trichloromethyl)-3-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
328104 |
| Chemical Formula | C8H4Cl3F3 |
| Molar Mass | 261.47 g/mol |
| Appearance | Liquid (usually) |
| Odor | Characteristic organic odor (speculative, needs verification) |
| Density | Data needed |
| Boiling Point | Data needed |
| Melting Point | Data needed |
| Solubility In Water | Insoluble (expected for non - polar organic compound) |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, toluene (expected) |
| Vapor Pressure | Data needed |
| Flash Point | Data needed |
| Stability | Stable under normal conditions (speculative, needs verification) |
| Hazard Class | Data needed |
As an accredited 1-(Trichloromethyl)-3-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500 - gram bottle packaging for 1-(trichloromethyl)-3-(trifluoromethyl)benzene. |
| Storage | 1-(Trichloromethyl)-3-(trifluoromethyl)benzene should be stored in a cool, well - ventilated area away from heat sources and ignition sources. It should be stored in a tightly - sealed container, preferably made of corrosion - resistant materials. Keep it separate from oxidizing agents and reactive chemicals to prevent potential reactions. Store in accordance with local safety regulations. |
| Shipping | 1-(Trichloromethyl)-3-(trifluoromethyl)benzene is a chemical. Shipping requires proper packaging in accordance with hazardous materials regulations to prevent leakage, ensuring safe transportation by approved carriers. |
Competitive 1-(Trichloromethyl)-3-(Trifluoromethyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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What are the physical properties of 1- (trichloromethyl) -3- (trifluoromethyl) benzene?
1 - (trifluoromethyl) - 3 - (trifluoromethyl) benzene, this substance is an organic compound with unique physical properties.
Looking at its properties, it is mostly colorless to slightly yellow liquid under normal conditions, with a clear and transparent appearance, like a mirror water stop, showing a pure state.
When it comes to boiling point, because the molecule contains many fluorine atoms, the electronegativity of fluorine atoms is extremely high, which enhances the intermolecular force, so its boiling point is relatively high, about a specific temperature range. This temperature gives the substance the stability of maintaining a liquid state under certain conditions. The melting point of
is also affected by fluorine atoms, showing a certain value, which is at the key node of the conversion between solid and liquid states, and determines its physical state at different temperatures.
In terms of solubility, due to the existence of fluorine atoms, the molecules have a certain polarity, which shows good solubility in organic solvents. It can be miscible with various organic solvents such as ethanol and ether, just like fish water, but the solubility in water is poor. It is difficult to overcome its own intermolecular force due to the force between water molecules.
The density is slightly larger than that of common organic solvents. Due to the increase in molecular weight due to fluorine atoms, the unit volume mass increases. In the liquid stratification experiment, the stratification phenomenon with low-density liquids can be clearly observed.
The volatility of benzene is lower than that of ordinary benzene compounds. Due to the large intermolecular force, the difficulty of molecules escaping from the liquid surface increases, and the volatilization rate in the air slows down. This property improves its stability during storage and use.
1- (trifluoromethyl) -3- (trifluoromethyl) The physical properties of benzene are significantly affected by the fluorine atoms in the molecular structure. These properties are of crucial significance in the fields of organic synthesis, materials science, etc., in the selection of reaction conditions, product separation and application.
Looking at its properties, it is mostly colorless to slightly yellow liquid under normal conditions, with a clear and transparent appearance, like a mirror water stop, showing a pure state.
When it comes to boiling point, because the molecule contains many fluorine atoms, the electronegativity of fluorine atoms is extremely high, which enhances the intermolecular force, so its boiling point is relatively high, about a specific temperature range. This temperature gives the substance the stability of maintaining a liquid state under certain conditions. The melting point of
is also affected by fluorine atoms, showing a certain value, which is at the key node of the conversion between solid and liquid states, and determines its physical state at different temperatures.
In terms of solubility, due to the existence of fluorine atoms, the molecules have a certain polarity, which shows good solubility in organic solvents. It can be miscible with various organic solvents such as ethanol and ether, just like fish water, but the solubility in water is poor. It is difficult to overcome its own intermolecular force due to the force between water molecules.
The density is slightly larger than that of common organic solvents. Due to the increase in molecular weight due to fluorine atoms, the unit volume mass increases. In the liquid stratification experiment, the stratification phenomenon with low-density liquids can be clearly observed.
The volatility of benzene is lower than that of ordinary benzene compounds. Due to the large intermolecular force, the difficulty of molecules escaping from the liquid surface increases, and the volatilization rate in the air slows down. This property improves its stability during storage and use.
1- (trifluoromethyl) -3- (trifluoromethyl) The physical properties of benzene are significantly affected by the fluorine atoms in the molecular structure. These properties are of crucial significance in the fields of organic synthesis, materials science, etc., in the selection of reaction conditions, product separation and application.
What are the chemical properties of 1- (trichloromethyl) -3- (trifluoromethyl) benzene?
1 - (trifluoromethyl) - 3 - (trifluoromethyl) benzene, which is an organic compound, has the following chemical properties:
First, because it contains a benzene ring, it has a certain aroma and can be like benzene. Electrophilic reagents are prone to attack the higher electron cloud density of the benzene ring. Common electrophilic substitution reactions such as halogenation reactions can react with halogen elemental substances under the catalysis of iron or iron salts, and halogen atoms replace hydrogen atoms on the benzene ring; there is also a nitration reaction, in the mixed acid of concentrated sulfuric acid and concentrated nitric acid, the benzene ring is introduced into the nitro group; sulfonation reaction, in the action of concentrated sulfuric acid, the benzene ring is connected to the sulfonic acid group.
Second, trifluoromethyl in its molecule is a strong electron-withdrawing group. Under this influence, the electron cloud density of the benzene ring decreases, so that the electrophilic substitution reaction activity decreases compared with benzene, and the substituents mainly enter the meta-position. This is because of the electron-withdrawing induction effect and conjugation effect of trifluoromethyl, the electron cloud density of the ortho and para-position of the benzene ring decreases more than that of the meta-position, and the electrophilic reagents tend to attack the meta-position.
Third, the carbon-fluorine bond energy in trifluoromethyl is relatively large and the properties are relatively stable. However, under certain conditions, such as high temperature and strong oxidant action, trifluoromethyl may react. Strong oxidants may fracture the carbon-fluorine bond, thereby trifluor Fourth, the compound has certain fat solubility and hydrophobicity due to fluorine atoms, and has good solubility in organic solvents. Its physical properties are also affected by fluorine atoms, and physical parameters such as boiling point and melting point are different from those of fluorine-free similar compounds.
First, because it contains a benzene ring, it has a certain aroma and can be like benzene. Electrophilic reagents are prone to attack the higher electron cloud density of the benzene ring. Common electrophilic substitution reactions such as halogenation reactions can react with halogen elemental substances under the catalysis of iron or iron salts, and halogen atoms replace hydrogen atoms on the benzene ring; there is also a nitration reaction, in the mixed acid of concentrated sulfuric acid and concentrated nitric acid, the benzene ring is introduced into the nitro group; sulfonation reaction, in the action of concentrated sulfuric acid, the benzene ring is connected to the sulfonic acid group.
Second, trifluoromethyl in its molecule is a strong electron-withdrawing group. Under this influence, the electron cloud density of the benzene ring decreases, so that the electrophilic substitution reaction activity decreases compared with benzene, and the substituents mainly enter the meta-position. This is because of the electron-withdrawing induction effect and conjugation effect of trifluoromethyl, the electron cloud density of the ortho and para-position of the benzene ring decreases more than that of the meta-position, and the electrophilic reagents tend to attack the meta-position.
Third, the carbon-fluorine bond energy in trifluoromethyl is relatively large and the properties are relatively stable. However, under certain conditions, such as high temperature and strong oxidant action, trifluoromethyl may react. Strong oxidants may fracture the carbon-fluorine bond, thereby trifluor Fourth, the compound has certain fat solubility and hydrophobicity due to fluorine atoms, and has good solubility in organic solvents. Its physical properties are also affected by fluorine atoms, and physical parameters such as boiling point and melting point are different from those of fluorine-free similar compounds.
In what fields is 1- (trichloromethyl) -3- (trifluoromethyl) benzene used?
1-% (trifluoromethyl) -3- (trifluoromethyl) benzene is used in many fields. In the field of medicine, due to its unique chemical structure, it has good fat solubility and electronic effects, which is conducive to drug molecules passing through biofilms and improving bioavailability. Taking the development of some new anti-cancer drugs as an example, the introduction of this structure can enhance the affinity of drugs with specific targets, accurately inhibit the growth and proliferation of cancer cells, improve the efficacy and reduce side effects.
In the field of materials science, it can be used to prepare high-performance fluoropolymer materials. With the strong electron absorption and low surface energy properties of trifluoromethyl, the prepared materials have excellent chemical stability, weather resistance and low coefficient of friction. For example, in the aerospace field, it is used to make aircraft wings and fuselage coating materials to resist harsh environmental erosion and reduce flight resistance.
In the field of pesticides, this structure can endow pesticide molecules with high-efficiency biological activity and environmental stability. After some new insecticides and fungicides are integrated into this structure, they can more effectively kill pests and pathogens, and have a short residual period in the environment, have little impact on the ecological environment, and ensure sustainable agricultural development.
In the field of electronic materials, compounds containing 1-% (trifluoromethyl) -3- (trifluoromethyl) benzene structure can be used to make organic semiconductor materials. Due to its unique electrical properties, it can enhance electron mobility and be used to fabricate high-performance organic field-effect transistors, organic Light Emitting Diodes, and other electronic devices, promoting the development of organic electronics.
In the field of materials science, it can be used to prepare high-performance fluoropolymer materials. With the strong electron absorption and low surface energy properties of trifluoromethyl, the prepared materials have excellent chemical stability, weather resistance and low coefficient of friction. For example, in the aerospace field, it is used to make aircraft wings and fuselage coating materials to resist harsh environmental erosion and reduce flight resistance.
In the field of pesticides, this structure can endow pesticide molecules with high-efficiency biological activity and environmental stability. After some new insecticides and fungicides are integrated into this structure, they can more effectively kill pests and pathogens, and have a short residual period in the environment, have little impact on the ecological environment, and ensure sustainable agricultural development.
In the field of electronic materials, compounds containing 1-% (trifluoromethyl) -3- (trifluoromethyl) benzene structure can be used to make organic semiconductor materials. Due to its unique electrical properties, it can enhance electron mobility and be used to fabricate high-performance organic field-effect transistors, organic Light Emitting Diodes, and other electronic devices, promoting the development of organic electronics.
What is the preparation method of 1- (trichloromethyl) -3- (trifluoromethyl) benzene?
To prepare 1 - (trichloromethyl) - 3 - (trichloromethyl) benzene, you can follow the following ancient method.
First take an appropriate amount of benzene and place it in a clean reactor. Using iron filings or anhydrous ferric trichloride as a catalyst, slowly introduce chlorine gas. This reaction needs to be carried out at an appropriate temperature and pressure, and the reaction process should be closely monitored. Chlorine gas reacts with benzene first to generate chlorobenzene.
Chlorobenzene has been obtained, and then in this reaction system, chlorine gas is continuously introduced, and the temperature is moderately increased and the pressure is adjusted. Because the hydrogen atom on the benzene ring is affected by the chlorine atom, the activity changes, so the chlorine atom can further replace the hydrogen atom at a specific position on the benzene ring, and gradually generate 1- (trichloromethyl) -3- (trichloromethyl) benzene.
After the reaction is completed, the reaction mixture is poured into the separation funnel, the product is extracted with an appropriate amount of organic solvent, and then purified by distillation, recrystallization, etc., to obtain pure 1- (trichloromethyl) -3- (trichloromethyl) benzene.
During the whole process, it is necessary to strictly abide by the operating procedures to ensure that the reaction conditions are precisely controlled. The equipment used must be clean and dry, and the purity of the raw material must also reach the corresponding standard. In this way, the ideal
First take an appropriate amount of benzene and place it in a clean reactor. Using iron filings or anhydrous ferric trichloride as a catalyst, slowly introduce chlorine gas. This reaction needs to be carried out at an appropriate temperature and pressure, and the reaction process should be closely monitored. Chlorine gas reacts with benzene first to generate chlorobenzene.
Chlorobenzene has been obtained, and then in this reaction system, chlorine gas is continuously introduced, and the temperature is moderately increased and the pressure is adjusted. Because the hydrogen atom on the benzene ring is affected by the chlorine atom, the activity changes, so the chlorine atom can further replace the hydrogen atom at a specific position on the benzene ring, and gradually generate 1- (trichloromethyl) -3- (trichloromethyl) benzene.
After the reaction is completed, the reaction mixture is poured into the separation funnel, the product is extracted with an appropriate amount of organic solvent, and then purified by distillation, recrystallization, etc., to obtain pure 1- (trichloromethyl) -3- (trichloromethyl) benzene.
During the whole process, it is necessary to strictly abide by the operating procedures to ensure that the reaction conditions are precisely controlled. The equipment used must be clean and dry, and the purity of the raw material must also reach the corresponding standard. In this way, the ideal
What are the environmental effects of 1- (trichloromethyl) -3- (trifluoromethyl) benzene?
"Tiangong Kaiwu" says: The influence of trichloromethyl on the environment is a matter that should be deeply investigated at the moment.
First, 1- (trichloromethyl) -3- (trichloromethyl) benzene, this is an organic compound with certain stability, but it also has many effects in the environment. In the atmosphere, it may participate in photochemical reactions. Under atmospheric light, such compounds may decompose to produce free radicals, which are highly active and can interact with other substances in the atmosphere, such as oxygen and nitrogen oxides, which in turn affect the balance of atmospheric chemistry and the stability of the ozone layer.
Furthermore, in the aquatic environment, if this substance does not enter the water body carelessly, due to its hydrophobicity, or is easily adsorbed on suspended particles, it will settle into the underwater sediments. In the long run, it may change the microenvironment of the underwater ecology and have an adverse impact on the survival and reproduction of aquatic organisms. If aquatic organisms ingest sediments containing this substance, it may accumulate in the body and pass along the food chain, endangering the health of higher trophic organisms.
And in the soil environment, 1- (trichloromethyl) -3- (trichloromethyl) benzene may affect the structure and function of soil microbial communities. Soil microorganisms play a key role in soil nutrient cycling and organic matter decomposition. The existence of this substance may inhibit the growth of some beneficial microorganisms, disrupt the normal operation of the soil ecosystem, and hinder the maintenance and improvement of soil fertility.
From this perspective, 1- (trichloromethyl) -3- (trichloromethyl) benzene has potential negative effects in the air, water and soil of the environment, and it needs to be treated with caution to reduce its harm to the ecological environment.
First, 1- (trichloromethyl) -3- (trichloromethyl) benzene, this is an organic compound with certain stability, but it also has many effects in the environment. In the atmosphere, it may participate in photochemical reactions. Under atmospheric light, such compounds may decompose to produce free radicals, which are highly active and can interact with other substances in the atmosphere, such as oxygen and nitrogen oxides, which in turn affect the balance of atmospheric chemistry and the stability of the ozone layer.
Furthermore, in the aquatic environment, if this substance does not enter the water body carelessly, due to its hydrophobicity, or is easily adsorbed on suspended particles, it will settle into the underwater sediments. In the long run, it may change the microenvironment of the underwater ecology and have an adverse impact on the survival and reproduction of aquatic organisms. If aquatic organisms ingest sediments containing this substance, it may accumulate in the body and pass along the food chain, endangering the health of higher trophic organisms.
And in the soil environment, 1- (trichloromethyl) -3- (trichloromethyl) benzene may affect the structure and function of soil microbial communities. Soil microorganisms play a key role in soil nutrient cycling and organic matter decomposition. The existence of this substance may inhibit the growth of some beneficial microorganisms, disrupt the normal operation of the soil ecosystem, and hinder the maintenance and improvement of soil fertility.
From this perspective, 1- (trichloromethyl) -3- (trichloromethyl) benzene has potential negative effects in the air, water and soil of the environment, and it needs to be treated with caution to reduce its harm to the ecological environment.
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