Linshang Chemical
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1,3-Dichloro-2-(Trifluoromethoxy)Benzene
Linshang Chemical
|
HS Code |
749418 |
| Chemical Formula | C7H3Cl2F3O |
| Molecular Weight | 230.999 |
| Appearance | Liquid (Typical) |
| Boiling Point | 185 - 186 °C |
| Density | 1.556 g/cm³ |
| Vapor Pressure | Low (Estimated) |
| Water Solubility | Insoluble |
| Flash Point | 77 °C |
| Refractive Index | 1.449 |
| Odor | Characteristic Aromatic Odor |
As an accredited 1,3-Dichloro-2-(Trifluoromethoxy)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 1,3 - dichloro - 2-(trifluoromethoxy)benzene packaged in a sealed, chemical - resistant bottle. |
| Storage | 1,3 - Dichloro - 2 - (trifluoromethoxy)benzene should be stored in a cool, well - ventilated area away from heat and ignition sources. Keep it in a tightly closed container, preferably made of corrosion - resistant materials due to its chemical nature. Store separately from oxidizing agents and incompatible substances to prevent potential reactions. |
| Shipping | 1,3 - dichloro - 2 - (trifluoromethoxy)benzene is shipped in specialized containers, ensuring proper sealing to prevent leakage. Transport follows strict chemical shipping regulations, with measures for safe handling and storage during transit. |
Competitive 1,3-Dichloro-2-(Trifluoromethoxy)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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What are the main uses of 1,3-dichloro-2- (trifluoromethoxy) benzene?
1% 2C3 -dioxy-2 - (triethoxyformyl) naphthalene, although this substance is not specifically mentioned in "Tiangong Kaiwu", it is based on ancient chemical technology and the use of the substance.
In ancient times, such organic compounds may have been useful in the preparation of dyes. Ancient dyeing processes were developed, and the production of dyes often involved a variety of chemical changes. Compounds containing special structures may be skillfully processed to produce key components of color. This naphthalene derivative, with its unique structure, may give fabrics a bright and lasting color, and has potential value in dyeing the clothes of dignitaries and pursuing unique color effects.
Furthermore, in some traditional medicine processing, it may also have traces. The ancients explored the medicinal uses of natural and synthetic substances in depth, and some organic compounds were specially processed, or had unique medicinal effects. Although their structures are complex, they can be reasonably compatible and refined, or can add new functions to the medicine, such as regulating qi and blood, treating sores, etc., or can play an auxiliary role.
Because of the exquisite production of ancient fragrances, complex organic compounds may add color to the preparation of fragrances. Its unique smell, or properly treated with other fragrances, creates an elegant and unique aroma, which is used for incense and sachet production to meet the needs of the ancients for aroma atmosphere creation.
In ancient times, such organic compounds may have been useful in the preparation of dyes. Ancient dyeing processes were developed, and the production of dyes often involved a variety of chemical changes. Compounds containing special structures may be skillfully processed to produce key components of color. This naphthalene derivative, with its unique structure, may give fabrics a bright and lasting color, and has potential value in dyeing the clothes of dignitaries and pursuing unique color effects.
Furthermore, in some traditional medicine processing, it may also have traces. The ancients explored the medicinal uses of natural and synthetic substances in depth, and some organic compounds were specially processed, or had unique medicinal effects. Although their structures are complex, they can be reasonably compatible and refined, or can add new functions to the medicine, such as regulating qi and blood, treating sores, etc., or can play an auxiliary role.
Because of the exquisite production of ancient fragrances, complex organic compounds may add color to the preparation of fragrances. Its unique smell, or properly treated with other fragrances, creates an elegant and unique aroma, which is used for incense and sachet production to meet the needs of the ancients for aroma atmosphere creation.
What are the physical properties of 1,3-dichloro-2- (trifluoromethoxy) benzene?
1% 2C3 -2- (triethoxy) silicon is one of the organosilicon compounds. Its physical properties are particularly important and affect the performance of many applications.
First of all, its phase state and appearance, under normal conditions, it is mostly colorless and transparent liquid, clear and clear, without significant impurities. This state is easy to observe and operate, and it is easy to control in many chemical processes.
times and boiling point, its boiling point is quite characteristic, about a certain temperature range, this boiling point value makes it possible to realize gas-liquid conversion under specific temperature conditions, which is conducive to distillation, separation and other process steps, and can be used to distinguish and purify from other substances.
Furthermore, density is also a key property. Its density is relatively stable and has a specific value. This value is of great significance in the preparation of solutions and the determination of dosage, etc., which is related to the accuracy of the reaction and the quality of the product.
Solubility cannot be ignored. 1% 2C3 -2- (triethoxy) silicon exhibits a certain solubility in common organic solvents and can be well miscible with some organic solvents. This property lays the foundation for its application in coatings, adhesives and other fields, allowing it to be evenly dispersed in the system and play its due role.
In addition, its viscosity also has unique features. The appropriate viscosity gives it good fluidity and coatability, and can evenly cover the surface of the substrate during the coating process, forming a uniform film layer to ensure the uniformity of product quality.
In summary, the physical properties of 1% 2C3 -dioxide- 2 - (triethoxy) silicon, such as phase state, boiling point, density, solubility, viscosity, etc., are interrelated and jointly determine its application in many fields such as chemical industry and materials. It is of great significance to industrial production and scientific research.
First of all, its phase state and appearance, under normal conditions, it is mostly colorless and transparent liquid, clear and clear, without significant impurities. This state is easy to observe and operate, and it is easy to control in many chemical processes.
times and boiling point, its boiling point is quite characteristic, about a certain temperature range, this boiling point value makes it possible to realize gas-liquid conversion under specific temperature conditions, which is conducive to distillation, separation and other process steps, and can be used to distinguish and purify from other substances.
Furthermore, density is also a key property. Its density is relatively stable and has a specific value. This value is of great significance in the preparation of solutions and the determination of dosage, etc., which is related to the accuracy of the reaction and the quality of the product.
Solubility cannot be ignored. 1% 2C3 -2- (triethoxy) silicon exhibits a certain solubility in common organic solvents and can be well miscible with some organic solvents. This property lays the foundation for its application in coatings, adhesives and other fields, allowing it to be evenly dispersed in the system and play its due role.
In addition, its viscosity also has unique features. The appropriate viscosity gives it good fluidity and coatability, and can evenly cover the surface of the substrate during the coating process, forming a uniform film layer to ensure the uniformity of product quality.
In summary, the physical properties of 1% 2C3 -dioxide- 2 - (triethoxy) silicon, such as phase state, boiling point, density, solubility, viscosity, etc., are interrelated and jointly determine its application in many fields such as chemical industry and materials. It is of great significance to industrial production and scientific research.
What are the chemical properties of 1,3-dichloro-2- (trifluoromethoxy) benzene?
1% 2C3 -dioxy-2 - (triethoxyformyl) naphthalene, this is an organic compound. Its chemical properties are quite unique and contain specific structures and reactivity.
From the structural point of view, the naphthalene ring is its core structure, which endows the compound with certain stability and conjugation properties. The conjugation system of the naphthalene ring makes the electron cloud distribution more uniform, which affects its physical and chemical properties. The introduction of dioxy groups changes the electron density and spatial configuration of the molecule. Oxygen atoms have high electronegativity, which can attract electrons, reduce the electron cloud density of the atoms or groups connected to them, and then affect the reactivity of the compound.
Triethoxyformyl groups are also key structural parts. The presence of ethoxy increases the lipophilicity of the molecule, while the carbonyl group of the formyl group has strong reactivity. Carbonyl carbons have a partial positive charge and are susceptible to attack by nucleophiles, resulting in reactions such as nucleophilic addition.
In chemical reactions, the compound may exhibit a variety of properties. Because it contains active groups, it can participate in substitution reactions. For example, nucleophiles or carbonyl carbons can be attacked to achieve the substitution of ethoxy groups and generate new compounds. The conjugated system of the naphthalene ring can also participate in some aromatic electrophilic substitution reactions. Under appropriate conditions, the electrophilic reagents can attack the naphthalene ring and introduce substituents at specific positions.
At the same time, the oxygen atoms in the compound can participate in the formation of hydrogen bonds, which affects its solubility in solution and intermolecular interactions. Its chemical properties make it potentially useful in the field of organic synthesis, and it can be used as an intermediate for the synthesis of more complex organic compounds, providing an important material basis for the study of organic synthetic chemistry.
From the structural point of view, the naphthalene ring is its core structure, which endows the compound with certain stability and conjugation properties. The conjugation system of the naphthalene ring makes the electron cloud distribution more uniform, which affects its physical and chemical properties. The introduction of dioxy groups changes the electron density and spatial configuration of the molecule. Oxygen atoms have high electronegativity, which can attract electrons, reduce the electron cloud density of the atoms or groups connected to them, and then affect the reactivity of the compound.
Triethoxyformyl groups are also key structural parts. The presence of ethoxy increases the lipophilicity of the molecule, while the carbonyl group of the formyl group has strong reactivity. Carbonyl carbons have a partial positive charge and are susceptible to attack by nucleophiles, resulting in reactions such as nucleophilic addition.
In chemical reactions, the compound may exhibit a variety of properties. Because it contains active groups, it can participate in substitution reactions. For example, nucleophiles or carbonyl carbons can be attacked to achieve the substitution of ethoxy groups and generate new compounds. The conjugated system of the naphthalene ring can also participate in some aromatic electrophilic substitution reactions. Under appropriate conditions, the electrophilic reagents can attack the naphthalene ring and introduce substituents at specific positions.
At the same time, the oxygen atoms in the compound can participate in the formation of hydrogen bonds, which affects its solubility in solution and intermolecular interactions. Its chemical properties make it potentially useful in the field of organic synthesis, and it can be used as an intermediate for the synthesis of more complex organic compounds, providing an important material basis for the study of organic synthetic chemistry.
What is the production method of 1,3-dichloro-2- (trifluoromethoxy) benzene?
The preparation method of 1% 2C3-dioxy-2- (triethoxyformyl) naphthalene, although it is not explicitly stated in Tiangong Kaiwu, it can be deduced from the chemical process ideas and similar production methods of the ancients.
In the past, the preparation of such compounds relied mostly on natural materials and ingenious chemical reactions. When organic synthesis was first developed, natural naphthalene-containing substances were often taken, such as some special plant extracts or coal tar fractions. Covered coal tar is a treasure trove of organic compounds, containing many aromatic hydrocarbons, of which naphthalene is the key component.
First, the naphthalene-containing raw materials were separated and purified by a suitable method. The ancients used distillation and extraction techniques, although the technology was simple at that time, they could still obtain relatively pure naphthalene.
Then, for the introduction of dioxy groups, or the method of oxidation. Oxygen in the air can be used, accompanied by a specific catalyst. In ancient times, although there was no modern precise catalyst, it was found that some metal oxides, such as copper and iron oxides, can promote the oxidation reaction. Under mild heating conditions, the naphthalene and oxygen were slowly interacted, and oxygen atoms were introduced at specific positions in the naphthalene ring to form a dioxy structure.
As for the introduction of (triethoxyformyl) groups, it can be achieved by esterification. Although there were no advanced chemical reagents at that time, natural acids and alcohols could be used. If the corresponding carboxylic acid and ethanol are used under the action of an acidic catalyst to form ethoxy formate. Then the ester is reacted with the dioxy-containing naphthalene derivative, and the (triethoxy formyl) group is successfully attached to the naphthalene ring under ingenious reaction conditions, such as controlling the temperature, reaction time and the proportion of the reactants.
In this process, the ancients used experience and repeated attempts to find suitable reaction conditions to achieve the purpose of preparing 1% 2C3 -dioxy-2- (triethoxy formyl) naphthalene. Although there is no precise theory and advanced equipment of modern chemistry, its wisdom and spirit of exploration have laid the foundation for future organic synthetic chemistry.
In the past, the preparation of such compounds relied mostly on natural materials and ingenious chemical reactions. When organic synthesis was first developed, natural naphthalene-containing substances were often taken, such as some special plant extracts or coal tar fractions. Covered coal tar is a treasure trove of organic compounds, containing many aromatic hydrocarbons, of which naphthalene is the key component.
First, the naphthalene-containing raw materials were separated and purified by a suitable method. The ancients used distillation and extraction techniques, although the technology was simple at that time, they could still obtain relatively pure naphthalene.
Then, for the introduction of dioxy groups, or the method of oxidation. Oxygen in the air can be used, accompanied by a specific catalyst. In ancient times, although there was no modern precise catalyst, it was found that some metal oxides, such as copper and iron oxides, can promote the oxidation reaction. Under mild heating conditions, the naphthalene and oxygen were slowly interacted, and oxygen atoms were introduced at specific positions in the naphthalene ring to form a dioxy structure.
As for the introduction of (triethoxyformyl) groups, it can be achieved by esterification. Although there were no advanced chemical reagents at that time, natural acids and alcohols could be used. If the corresponding carboxylic acid and ethanol are used under the action of an acidic catalyst to form ethoxy formate. Then the ester is reacted with the dioxy-containing naphthalene derivative, and the (triethoxy formyl) group is successfully attached to the naphthalene ring under ingenious reaction conditions, such as controlling the temperature, reaction time and the proportion of the reactants.
In this process, the ancients used experience and repeated attempts to find suitable reaction conditions to achieve the purpose of preparing 1% 2C3 -dioxy-2- (triethoxy formyl) naphthalene. Although there is no precise theory and advanced equipment of modern chemistry, its wisdom and spirit of exploration have laid the foundation for future organic synthetic chemistry.
What are the precautions for the use of 1,3-dichloro-2- (trifluoromethoxy) benzene?
1% 2C3-dioxy-2- (triethoxy) silicon should pay attention to the following matters during use:
First, it is related to storage. This substance should be stored in a cool, dry and well-ventilated place. It must not come into contact with water or moisture. It is prone to hydrolysis reaction in contact with water, resulting in deterioration and thus affecting its performance. It needs to be tightly sealed in a specific container to prevent external factors from interfering.
Second, caution should be taken during operation. During access and use, wear appropriate protective equipment, such as gloves, goggles, etc. Because it may be irritating to the skin and eyes, if you come into contact accidentally, you should immediately rinse with a large amount of water and seek medical treatment in a timely manner. And the operation should be carried out in a fume hood to prevent inhalation of volatile aerosols, so as not to endanger respiratory health.
Third, it involves the reaction conditions. When participating in a chemical reaction, it is necessary to precisely control the reaction temperature, time and proportion of the reactants. Different reaction conditions have a great impact on the reaction process and the quality of the product. For example, if the temperature is too high, or side reactions are triggered, the purity of the product is damaged; if the reaction time is insufficient, the reaction may be incomplete.
Fourth, compatibility taboos cannot be ignored. Be sure to check its compatibility with other chemical substances, some substances mix with it, or react violently, or even cause dangerous conditions. Before mixing it with other reagents, be sure to pass reliable data or experiments to confirm whether the two are compatible.
Fifth, disposal after use. The remaining materials should not be discarded at will, and should be properly disposed of in accordance with relevant regulations. The used containers should also be thoroughly cleaned to prevent residual substances from affecting subsequent use.
All these precautions require the user's careful attention to ensure the safety and efficacy of 1% 2C3-dioxide-2- (triethoxy) silicon during use.
First, it is related to storage. This substance should be stored in a cool, dry and well-ventilated place. It must not come into contact with water or moisture. It is prone to hydrolysis reaction in contact with water, resulting in deterioration and thus affecting its performance. It needs to be tightly sealed in a specific container to prevent external factors from interfering.
Second, caution should be taken during operation. During access and use, wear appropriate protective equipment, such as gloves, goggles, etc. Because it may be irritating to the skin and eyes, if you come into contact accidentally, you should immediately rinse with a large amount of water and seek medical treatment in a timely manner. And the operation should be carried out in a fume hood to prevent inhalation of volatile aerosols, so as not to endanger respiratory health.
Third, it involves the reaction conditions. When participating in a chemical reaction, it is necessary to precisely control the reaction temperature, time and proportion of the reactants. Different reaction conditions have a great impact on the reaction process and the quality of the product. For example, if the temperature is too high, or side reactions are triggered, the purity of the product is damaged; if the reaction time is insufficient, the reaction may be incomplete.
Fourth, compatibility taboos cannot be ignored. Be sure to check its compatibility with other chemical substances, some substances mix with it, or react violently, or even cause dangerous conditions. Before mixing it with other reagents, be sure to pass reliable data or experiments to confirm whether the two are compatible.
Fifth, disposal after use. The remaining materials should not be discarded at will, and should be properly disposed of in accordance with relevant regulations. The used containers should also be thoroughly cleaned to prevent residual substances from affecting subsequent use.
All these precautions require the user's careful attention to ensure the safety and efficacy of 1% 2C3-dioxide-2- (triethoxy) silicon during use.
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