Linshang Chemical
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1,4-Dichloro-2-(Trifluoromethyl)Benzene
Linshang Chemical
|
HS Code |
712388 |
| Chemical Formula | C7H3Cl2F3 |
| Molecular Weight | 215.00 |
| Appearance | Colorless to light yellow liquid |
| Boiling Point | 176 - 178 °C |
| Density | 1.476 g/cm³ |
| Water Solubility | Insoluble |
| Flash Point | 65 °C |
| Odor | Characteristic aromatic odor |
| Stability | Stable under normal conditions |
| Flammability | Combustible |
As an accredited 1,4-Dichloro-2-(Trifluoromethyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1,4 - dichloro - 2-(trifluoromethyl)benzene: Packed in 5 - kg drums for chemical storage. |
| Storage | 1,4 - Dichloro - 2 - (trifluoromethyl)benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, flames, and oxidizing agents. Store in a tightly sealed container, preferably made of corrosion - resistant materials, to prevent leakage and exposure to air and moisture, which could potentially lead to chemical reactions or degradation. |
| Shipping | 1,4 - dichloro - 2 - (trifluoromethyl)benzene is shipped in tightly sealed, corrosion - resistant containers. Special handling is required due to its chemical nature, following strict regulations for transporting hazardous chemicals. |
Competitive 1,4-Dichloro-2-(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.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy 1,4-Dichloro-2-(Trifluoromethyl)Benzene in China?
As a trusted 1,4-Dichloro-2-(Trifluoromethyl)Benzene manufacturer, we deliver:
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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 1,4-Dichloro-2-(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 1,4-dichloro-2- (trifluoromethyl) benzene?
1% 2C4-dioxy-2- (triethoxy) benzene, which is widely used. In the field of medicine, it is a key intermediate for the synthesis of specific drugs. With its unique chemical structure, it can participate in a series of reactions and help build complex drug molecular structures, which is of great significance for the creation of new drugs and the improvement of drug efficacy.
In the field of materials science, it is often used as a raw material for the synthesis of functional materials. For example, through specific reactions, polymer materials with special optical and electrical properties can be prepared, which shows important value in optical devices, electronic components and other fields, or can improve material stability, conductivity and other properties, and broaden the application range of materials. In the field of organic synthetic chemistry, as a basic raw material, it can participate in many organic reactions and provide an effective path for the synthesis of complex organic compounds. Due to its specific functional groups and reactivity, it provides convenience for organic chemists to construct diverse organic molecular structures, promotes the development of organic synthetic chemistry, and helps to synthesize more novel organic compounds with special properties.
In the field of materials science, it is often used as a raw material for the synthesis of functional materials. For example, through specific reactions, polymer materials with special optical and electrical properties can be prepared, which shows important value in optical devices, electronic components and other fields, or can improve material stability, conductivity and other properties, and broaden the application range of materials. In the field of organic synthetic chemistry, as a basic raw material, it can participate in many organic reactions and provide an effective path for the synthesis of complex organic compounds. Due to its specific functional groups and reactivity, it provides convenience for organic chemists to construct diverse organic molecular structures, promotes the development of organic synthetic chemistry, and helps to synthesize more novel organic compounds with special properties.
What are the physical properties of 1,4-dichloro-2- (trifluoromethyl) benzene?
1% 2C4 -dioxy-2- (triethoxy) benzene is one of the organic compounds. Its physical properties are unique, let me tell you in detail.
Looking at its properties, under room temperature and pressure, 1% 2C4 -dioxy-2- (triethoxy) benzene is mostly colorless to light yellow liquid, with a clear and transparent texture, like water from a clear spring, with a warm luster. Close to the smell, there is a faint aromatic smell, but this fragrance is not rich and strong, but fresh and elegant, just like the faint floral fragrance floating in the spring breeze. Although it is not flamboyant, it also attracts attention.
When it comes to melting point, the melting point of this compound is quite low, and it can still maintain a liquid state in an ordinary low temperature environment. Just like ice and snow are easy to melt under warm sunlight, when it is at a lower temperature, it does not have the shape of a solid state. In terms of boiling point, its boiling point is relatively moderate. If it is heated, when the temperature rises to a specific degree, it can be seen that it slowly converts from liquid to gaseous state, such as cloud evaporation, turning into invisible gas floating in the air.
In addition, its density also has characteristics. Compared with the density of water, it is either light or heavy, and it has its own unique value. Just as things of different materials float and float differently in water, 1% 2C4-dioxy-2- (triethoxy) benzene, when mixed with liquids such as water, either floats on water or sinks under water according to its density differences, showing a different state.
Solubility is also an important physical property. 1% 2C4-dioxy-2- (triethoxy) benzene in organic solvents, such as fish in water, can be well dissolved in it, and blend with organic solvents, as if they are integrated. However, in water, its solubility is quite limited, and the two are difficult to fully integrate. It seems that oil and water are incompatible, and only a little dispersed state can be seen.
In summary, the physical properties of 1% 2C4-dioxy-2- (triethoxy) benzene, from their properties to their melting point, boiling point, density, and solubility, are unique and constitute distinct characteristics.
Looking at its properties, under room temperature and pressure, 1% 2C4 -dioxy-2- (triethoxy) benzene is mostly colorless to light yellow liquid, with a clear and transparent texture, like water from a clear spring, with a warm luster. Close to the smell, there is a faint aromatic smell, but this fragrance is not rich and strong, but fresh and elegant, just like the faint floral fragrance floating in the spring breeze. Although it is not flamboyant, it also attracts attention.
When it comes to melting point, the melting point of this compound is quite low, and it can still maintain a liquid state in an ordinary low temperature environment. Just like ice and snow are easy to melt under warm sunlight, when it is at a lower temperature, it does not have the shape of a solid state. In terms of boiling point, its boiling point is relatively moderate. If it is heated, when the temperature rises to a specific degree, it can be seen that it slowly converts from liquid to gaseous state, such as cloud evaporation, turning into invisible gas floating in the air.
In addition, its density also has characteristics. Compared with the density of water, it is either light or heavy, and it has its own unique value. Just as things of different materials float and float differently in water, 1% 2C4-dioxy-2- (triethoxy) benzene, when mixed with liquids such as water, either floats on water or sinks under water according to its density differences, showing a different state.
Solubility is also an important physical property. 1% 2C4-dioxy-2- (triethoxy) benzene in organic solvents, such as fish in water, can be well dissolved in it, and blend with organic solvents, as if they are integrated. However, in water, its solubility is quite limited, and the two are difficult to fully integrate. It seems that oil and water are incompatible, and only a little dispersed state can be seen.
In summary, the physical properties of 1% 2C4-dioxy-2- (triethoxy) benzene, from their properties to their melting point, boiling point, density, and solubility, are unique and constitute distinct characteristics.
Is the chemical properties of 1,4-dichloro-2- (trifluoromethyl) benzene stable?
The chemical properties of 1% 2C4-dihydro-2- (triethoxy methyl) naphthalene are quite stable.
Looking at the structure of this compound, the skeleton of 1% 2C4-dihydro naphthalene gives it a certain conjugation stability. Although the dihydro-naphthalene part is not a fully conjugated aromatic system, its presence gives the molecule a special electron cloud distribution and can resist the attack of some common chemical reactions.
The substituent of 2 - (triethoxy methyl) also contributes significantly to its stability. In the triethoxy methyl group, the ethoxy group is connected to the methyl group, and the ethoxy group forms a electron supply effect with the connected carbon atom of the oxygen atom, which increases the electron cloud density around the substituent group. This change in electron cloud density can stabilize the overall structure of the molecule and reduce its reactivity to electrophilic and nucleophilic reagents.
In terms of spatial structure, the large steric resistance of the triethoxy methyl group hinders the external reagent from approaching the core of the molecule to a certain extent, thereby further enhancing the stability of the compound. Therefore, under normal conditions, the chemical properties of 1% 2C4 -dihydro-2- (triethoxy methyl) naphthalene are relatively stable, and it is not easy to cause violent chemical reactions.
Looking at the structure of this compound, the skeleton of 1% 2C4-dihydro naphthalene gives it a certain conjugation stability. Although the dihydro-naphthalene part is not a fully conjugated aromatic system, its presence gives the molecule a special electron cloud distribution and can resist the attack of some common chemical reactions.
The substituent of 2 - (triethoxy methyl) also contributes significantly to its stability. In the triethoxy methyl group, the ethoxy group is connected to the methyl group, and the ethoxy group forms a electron supply effect with the connected carbon atom of the oxygen atom, which increases the electron cloud density around the substituent group. This change in electron cloud density can stabilize the overall structure of the molecule and reduce its reactivity to electrophilic and nucleophilic reagents.
In terms of spatial structure, the large steric resistance of the triethoxy methyl group hinders the external reagent from approaching the core of the molecule to a certain extent, thereby further enhancing the stability of the compound. Therefore, under normal conditions, the chemical properties of 1% 2C4 -dihydro-2- (triethoxy methyl) naphthalene are relatively stable, and it is not easy to cause violent chemical reactions.
What are the synthesis methods of 1,4-dichloro-2- (trifluoromethyl) benzene?
To prepare 1% 2C4-dihydroxy-2- (triethoxy) benzene, the method is as follows:
First, start with suitable raw materials. It is common to take a benzene derivative with a specific structure as the initial substrate. This substrate needs to contain a modifiable group for subsequent introduction of hydroxyl groups and triethoxy groups.
times, the hydroxylation reaction is carried out. It is often possible to use a specific combination of oxidizing agent and catalyst to promote the introduction of hydroxyl groups into the benzene ring at the 1,4 positions. This process requires careful temperature control, timing control, and control of the proportion of reactants. For example, select a strong oxidizing reagent, under mild heating conditions, slowly add it dropwise to the reaction system of the substrate, during which a suitable monitoring means, such as thin-layer chromatography, is used to observe the reaction process, to the 1, 4 hydroxylated products reach the expected proportion.
Then, triethoxy is introduced. Generally, reagents containing ethoxy groups, such as triethoxy boron, are taken to react with hydroxylated benzene derivatives in a base-catalyzed environment. The base can help the reagent to form an active intermediate, which is easier to bind to the substrate. During the reaction, the drying of the system and the protection of inert gas are maintained to prevent side reactions.
Repeat, after the reaction is completed, the product needs to be separated and purified. The product can be extracted from the reaction mixture by extraction method first with a suitable organic solvent. After column chromatography, the suitable stationary phase and mobile phase were selected, and the product was further purified to obtain pure 1% 2C4-dihydroxy-2- (triethoxy) benzene.
The whole synthesis process requires fine operation at each step, close monitoring, and careful regulation of reaction conditions according to reaction characteristics and product requirements to obtain the target product.
First, start with suitable raw materials. It is common to take a benzene derivative with a specific structure as the initial substrate. This substrate needs to contain a modifiable group for subsequent introduction of hydroxyl groups and triethoxy groups.
times, the hydroxylation reaction is carried out. It is often possible to use a specific combination of oxidizing agent and catalyst to promote the introduction of hydroxyl groups into the benzene ring at the 1,4 positions. This process requires careful temperature control, timing control, and control of the proportion of reactants. For example, select a strong oxidizing reagent, under mild heating conditions, slowly add it dropwise to the reaction system of the substrate, during which a suitable monitoring means, such as thin-layer chromatography, is used to observe the reaction process, to the 1, 4 hydroxylated products reach the expected proportion.
Then, triethoxy is introduced. Generally, reagents containing ethoxy groups, such as triethoxy boron, are taken to react with hydroxylated benzene derivatives in a base-catalyzed environment. The base can help the reagent to form an active intermediate, which is easier to bind to the substrate. During the reaction, the drying of the system and the protection of inert gas are maintained to prevent side reactions.
Repeat, after the reaction is completed, the product needs to be separated and purified. The product can be extracted from the reaction mixture by extraction method first with a suitable organic solvent. After column chromatography, the suitable stationary phase and mobile phase were selected, and the product was further purified to obtain pure 1% 2C4-dihydroxy-2- (triethoxy) benzene.
The whole synthesis process requires fine operation at each step, close monitoring, and careful regulation of reaction conditions according to reaction characteristics and product requirements to obtain the target product.
What are the precautions for storing and transporting 1,4-dichloro-2- (trifluoromethyl) benzene?
1% 2C4-dioxy-2- (triethoxy) benzene, when storing and transporting, pay attention to many matters.
First, because of its certain chemical activity, it may burn in case of heat or open flame, so the storage place must be far away from fire and heat sources, keep cool and well ventilated. Just like the ancients hid things in a secluded place, to avoid the disturbance of sun and fire.
Second, this material has strict requirements on packaging materials. The packaging used needs to be able to be effectively sealed to prevent leakage. If the packaging is not good, the leaked material may react with the surrounding materials, causing an accident, just like a tightly sealed treasure, so as not to expose damage.
Third, when transporting, be sure to follow specific rules. The handling process must be handled with care, and cannot be loaded and unloaded brutally to avoid damage to the packaging. Just like escorting fragile porcelain, proceed with caution.
Fourth, the humidity of the storage environment should also be paid attention to. If the humidity is too high or affects its chemical properties, it should be stored in a dry place, just like an ancient book collection, in a dry place to prevent mildew.
Fifth, those who come into contact with it should be well protected. Because it may be irritating to the human body, the operation should be equipped with appropriate protective equipment, such as gloves, goggles, etc., like a soldier going into battle, wearing a sharp armor to protect himself.
All of these should be taken into account when storing and transporting 1% 2C4 -dioxy-2- (triethoxy) benzene and should not be ignored.
First, because of its certain chemical activity, it may burn in case of heat or open flame, so the storage place must be far away from fire and heat sources, keep cool and well ventilated. Just like the ancients hid things in a secluded place, to avoid the disturbance of sun and fire.
Second, this material has strict requirements on packaging materials. The packaging used needs to be able to be effectively sealed to prevent leakage. If the packaging is not good, the leaked material may react with the surrounding materials, causing an accident, just like a tightly sealed treasure, so as not to expose damage.
Third, when transporting, be sure to follow specific rules. The handling process must be handled with care, and cannot be loaded and unloaded brutally to avoid damage to the packaging. Just like escorting fragile porcelain, proceed with caution.
Fourth, the humidity of the storage environment should also be paid attention to. If the humidity is too high or affects its chemical properties, it should be stored in a dry place, just like an ancient book collection, in a dry place to prevent mildew.
Fifth, those who come into contact with it should be well protected. Because it may be irritating to the human body, the operation should be equipped with appropriate protective equipment, such as gloves, goggles, etc., like a soldier going into battle, wearing a sharp armor to protect himself.
All of these should be taken into account when storing and transporting 1% 2C4 -dioxy-2- (triethoxy) benzene and should not be ignored.
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