Linshang Chemical
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1,1'-[Chloro(Phenyl)Methanediyl]Bis(4-Methoxybenzene)
Linshang Chemical
|
HS Code |
832830 |
| Chemical Formula | C21H19ClO2 |
| Molar Mass | 338.83 g/mol |
| Appearance | Solid (usually white or off - white) |
| Physical State At Room Temp | Solid |
| Melting Point | Typically in a certain temperature range (exact value may vary by source) |
| Boiling Point | Higher boiling point due to molecular structure |
| Solubility In Water | Low solubility in water |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
| Density | Value depending on the form and purity |
| Stability | Stable under normal conditions, but may react with strong oxidizing agents |
As an accredited 1,1'-[Chloro(Phenyl)Methanediyl]Bis(4-Methoxybenzene) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1,1'-[chloro(phenyl)methanediyl]bis(4 - methoxybenzene) in sealed chemical - grade container. |
| Storage | 1,1'-[Chloro(phenyl)methanediyl]bis(4 - methoxybenzene) 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 to prevent moisture absorption and potential degradation. It is advisable to store it in a dedicated chemical storage facility following safety regulations. |
| Shipping | 1,1'-[Chloro(phenyl)methanediyl]bis(4 - methoxybenzene) is shipped in well - sealed, corrosion - resistant containers. It follows strict chemical shipping regulations to ensure safety during transit, protecting from physical damage and environmental exposure. |
Competitive 1,1'-[Chloro(Phenyl)Methanediyl]Bis(4-Methoxybenzene) 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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Where to Buy 1,1'-[Chloro(Phenyl)Methanediyl]Bis(4-Methoxybenzene) in China?
As a trusted 1,1'-[Chloro(Phenyl)Methanediyl]Bis(4-Methoxybenzene) 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 1,1'-[Chloro(Phenyl)Methanediyl]Bis(4-Methoxybenzene) supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What is the main use of 1,1 '- [chloro (phenyl) methanediyl] bis (4-methoxybenzene)
1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29, this is an organic compound, most people call it by its English name, or simply call it a chloroaryl compound with a specific structure. Its main uses cover the following ends.
First, in the field of organic synthesis, it is often used as a key intermediate. As "Tiangong Kaiwu" said, "everything in the world can breed new things". This compound can be combined with many reagents through specific chemical reactions. After delicate steps, various organic products with complex structures and wide uses can be obtained. With its unique structure, chemists can introduce chlorine atoms and groups such as phenyl and methoxybenzene, paving the way for the construction of new organic molecules, just like skilled craftsmen build magnificent buildings with unique components.
Second, in the field of materials science, it is also of considerable value. Or due to the synergistic action of various groups in the molecule, it is endowed with special physical and chemical properties, such as affecting the optical and electrical properties of the material. It can be used to prepare materials with specific optoelectronic properties, just like the discovery and utilization of material properties in "Tiangong Kaiji". This compound can be rationally designed and processed, or it can contribute to the research and development of advanced materials, such as applications in organic Light Emitting Diodes, semiconductor materials and other fields.
Third, in pharmaceutical chemistry research, its unique structure may provide inspiration for drug development. The molecular design of some drugs often draws on such chlorine-containing and aryl structures, hoping to develop new and effective drugs by simulating their active sites or spatial structures to solve the pain of diseases, just as the ancients studied the properties of herbs to cure diseases. Nowadays, such compounds are also used to explore new medical prescriptions.
First, in the field of organic synthesis, it is often used as a key intermediate. As "Tiangong Kaiwu" said, "everything in the world can breed new things". This compound can be combined with many reagents through specific chemical reactions. After delicate steps, various organic products with complex structures and wide uses can be obtained. With its unique structure, chemists can introduce chlorine atoms and groups such as phenyl and methoxybenzene, paving the way for the construction of new organic molecules, just like skilled craftsmen build magnificent buildings with unique components.
Second, in the field of materials science, it is also of considerable value. Or due to the synergistic action of various groups in the molecule, it is endowed with special physical and chemical properties, such as affecting the optical and electrical properties of the material. It can be used to prepare materials with specific optoelectronic properties, just like the discovery and utilization of material properties in "Tiangong Kaiji". This compound can be rationally designed and processed, or it can contribute to the research and development of advanced materials, such as applications in organic Light Emitting Diodes, semiconductor materials and other fields.
Third, in pharmaceutical chemistry research, its unique structure may provide inspiration for drug development. The molecular design of some drugs often draws on such chlorine-containing and aryl structures, hoping to develop new and effective drugs by simulating their active sites or spatial structures to solve the pain of diseases, just as the ancients studied the properties of herbs to cure diseases. Nowadays, such compounds are also used to explore new medical prescriptions.
What are the physical properties of 1,1 '- [chloro (phenyl) methanediyl] bis (4-methoxybenzene)
1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29 is an organic compound commonly known as chlorobenzyl ether. This compound has unique physical properties, which are described in detail by you today.
First of all, under room temperature and pressure, it is mostly white to light yellow crystalline powder. It is delicate and uniform, and has a certain luster. It seems to hide the mystery of the microscopic world.
Second, the melting point is about 88-92 degrees Celsius. When the temperature approaches this range, the thermal motion of the molecule intensifies, the lattice structure gradually disintegrates, and the solid state slowly melts into a liquid state. This phase transition process follows the laws of thermodynamics and molecular dynamics.
Furthermore, it involves its solubility, and it has a certain solubility in organic solvents, such as ethanol, acetone, chloroform, etc. Due to the interaction between groups such as benzene ring and methoxy group in the molecular structure and organic solvent molecules, such as van der Waals force and hydrogen bond, it can be dispersed in the solvent system, but the solubility in water is extremely low. Because the polarity of water does not match the structural polarity of the compound, it is difficult for water molecules to form effective interactions with the compound molecules.
In addition, its volatility is very small, and it is difficult to see significant volatilization in the air at room temperature. Due to the strong intermolecular force, the molecule needs high energy to escape from the liquid phase or the solid phase into the gas phase, so it can exist relatively stably in the solid or liquid state at room temperature.
The physical properties of this compound are closely related to its molecular structure. The benzene ring endows it with a certain rigidity and conjugate system, while the chlorine atom and methoxy group affect the molecular polarity and electron cloud distribution, resulting in the above unique physical properties.
First of all, under room temperature and pressure, it is mostly white to light yellow crystalline powder. It is delicate and uniform, and has a certain luster. It seems to hide the mystery of the microscopic world.
Second, the melting point is about 88-92 degrees Celsius. When the temperature approaches this range, the thermal motion of the molecule intensifies, the lattice structure gradually disintegrates, and the solid state slowly melts into a liquid state. This phase transition process follows the laws of thermodynamics and molecular dynamics.
Furthermore, it involves its solubility, and it has a certain solubility in organic solvents, such as ethanol, acetone, chloroform, etc. Due to the interaction between groups such as benzene ring and methoxy group in the molecular structure and organic solvent molecules, such as van der Waals force and hydrogen bond, it can be dispersed in the solvent system, but the solubility in water is extremely low. Because the polarity of water does not match the structural polarity of the compound, it is difficult for water molecules to form effective interactions with the compound molecules.
In addition, its volatility is very small, and it is difficult to see significant volatilization in the air at room temperature. Due to the strong intermolecular force, the molecule needs high energy to escape from the liquid phase or the solid phase into the gas phase, so it can exist relatively stably in the solid or liquid state at room temperature.
The physical properties of this compound are closely related to its molecular structure. The benzene ring endows it with a certain rigidity and conjugate system, while the chlorine atom and methoxy group affect the molecular polarity and electron cloud distribution, resulting in the above unique physical properties.
What are the chemical properties of 1,1 '- [chloro (phenyl) methanediyl] bis (4-methoxybenzene)
1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29, this is the name of an organic compound. According to its name, its structure contains chlorine, phenyl, methyldiyl and two 4-methoxyphenyl groups.
Looking at its chemical properties, it has the characteristics of chlorine atoms or halogenated hydrocarbons. Chlorine atoms are highly active and can participate in nucleophilic substitution reactions. Under appropriate conditions, chlorine atoms can be replaced by other nucleophilic reagents, such as hydroxyl and amino groups, and then different compounds can be derived.
Furthermore, the structure of the benzene ring gives it aromaticity. The benzene ring is stable and does not easily undergo addition reactions, but is prone to electrophilic substitution reactions. Electrophilic substitution reactions such as halogenation, nitrification, and sulfonation may occur on the benzene ring. And the methoxy group is the power supply group, which can increase the electron cloud density of the benzene ring, make the electrophilic substitution reaction easier to carry out, and the reaction check point may be mainly concentrated in the adjacent and para-position of the methoxy group.
In addition, two 4-methoxy phenyl groups in the molecule are connected by chlorine-containing methyl digroups, which may affect the spatial configuration and physical properties of the molecule. Or due to the steric resistance, it also has a certain impact on its reactivity and chemical properties. Its solubility or is affected by the polarity of the molecule, the methoxy group has a certain polarity, but the whole molecule is more soluble in organic solvents or better than water due to the existence of the benzene ring.
In summary, 1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29 has some chemical properties of halogenated hydrocarbons and aromatic compounds due to its unique structure, and may have potential application value in organic synthesis and other fields.
Looking at its chemical properties, it has the characteristics of chlorine atoms or halogenated hydrocarbons. Chlorine atoms are highly active and can participate in nucleophilic substitution reactions. Under appropriate conditions, chlorine atoms can be replaced by other nucleophilic reagents, such as hydroxyl and amino groups, and then different compounds can be derived.
Furthermore, the structure of the benzene ring gives it aromaticity. The benzene ring is stable and does not easily undergo addition reactions, but is prone to electrophilic substitution reactions. Electrophilic substitution reactions such as halogenation, nitrification, and sulfonation may occur on the benzene ring. And the methoxy group is the power supply group, which can increase the electron cloud density of the benzene ring, make the electrophilic substitution reaction easier to carry out, and the reaction check point may be mainly concentrated in the adjacent and para-position of the methoxy group.
In addition, two 4-methoxy phenyl groups in the molecule are connected by chlorine-containing methyl digroups, which may affect the spatial configuration and physical properties of the molecule. Or due to the steric resistance, it also has a certain impact on its reactivity and chemical properties. Its solubility or is affected by the polarity of the molecule, the methoxy group has a certain polarity, but the whole molecule is more soluble in organic solvents or better than water due to the existence of the benzene ring.
In summary, 1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29 has some chemical properties of halogenated hydrocarbons and aromatic compounds due to its unique structure, and may have potential application value in organic synthesis and other fields.
What is the production method of 1,1 '- [chloro (phenyl) methanediyl] bis (4-methoxybenzene)
To make 1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29, the following method is often followed.
First take an appropriate amount of 4-methoxybenzene and place it in a clean reaction vessel. In this vessel, add a specific catalyst, which needs to be carefully selected according to the characteristics and conditions of the reaction to promote the smooth subsequent reaction.
Then slowly inject the benzoyl reactants containing chlorine. When injecting, be sure to pay attention to the speed to avoid excessive reaction. The reaction system needs to be maintained in a specific temperature range, which may need to be controlled by a precise temperature control device. If the temperature is too high or too low, the reaction can deviate from the expected.
During the reaction process, stirring should be continued to make the reactants fully mixed and the reaction proceed uniformly. When the reaction reaches a certain extent, the product is separated from the reaction mixing system by suitable separation means, such as extraction, distillation, etc.
The separated product still needs to be purified. The method of recrystallization can be used to select a suitable solvent, so that the product can be dissolved and recrystallized in it to remove impurities and improve the purity of the product. After these steps, 1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29 can be obtained. During the whole process, the control of the conditions of each link is the key, and a slight difference will affect the quality and quantity of the product.
First take an appropriate amount of 4-methoxybenzene and place it in a clean reaction vessel. In this vessel, add a specific catalyst, which needs to be carefully selected according to the characteristics and conditions of the reaction to promote the smooth subsequent reaction.
Then slowly inject the benzoyl reactants containing chlorine. When injecting, be sure to pay attention to the speed to avoid excessive reaction. The reaction system needs to be maintained in a specific temperature range, which may need to be controlled by a precise temperature control device. If the temperature is too high or too low, the reaction can deviate from the expected.
During the reaction process, stirring should be continued to make the reactants fully mixed and the reaction proceed uniformly. When the reaction reaches a certain extent, the product is separated from the reaction mixing system by suitable separation means, such as extraction, distillation, etc.
The separated product still needs to be purified. The method of recrystallization can be used to select a suitable solvent, so that the product can be dissolved and recrystallized in it to remove impurities and improve the purity of the product. After these steps, 1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29 can be obtained. During the whole process, the control of the conditions of each link is the key, and a slight difference will affect the quality and quantity of the product.
1,1 '- [chloro (phenyl) methanediyl] bis (4-methoxybenzene) What are the precautions during use?
1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29 is an organic compound, and all precautions must be paid attention to during use.
Bear the brunt, and safety protection must be comprehensive. This compound may be toxic and irritating, and protective equipment such as gloves, goggles and masks are indispensable when operating to protect the skin, eyes and respiratory tract from damage.
Furthermore, the use of this compound should be carried out in a well-ventilated place or in a fume hood to prevent the accumulation of harmful gases and endanger personal safety. When weighing and transferring, the action should be precise and careful to avoid its spilling or splashing.
Storage should also not be underestimated. It must be placed in a cool, dry place away from ignition and oxidants to prevent deterioration or dangerous reactions.
In addition, chemical properties are also exquisite. When it participates in the reaction, the reaction conditions are strict, and factors such as temperature, pH and reaction time will affect the reaction effect and product purity. Before use, be sure to be familiar with its reaction characteristics and possible side reactions in order to be fully prepared.
At the same time, the waste generated during use should not be discarded at will, and it should be properly disposed of in accordance with relevant regulations to avoid environmental pollution.
In short, when using 1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29, we must be cautious and strictly abide by safety regulations and operating procedures to ensure safety and smooth progress of experiments or production.
Bear the brunt, and safety protection must be comprehensive. This compound may be toxic and irritating, and protective equipment such as gloves, goggles and masks are indispensable when operating to protect the skin, eyes and respiratory tract from damage.
Furthermore, the use of this compound should be carried out in a well-ventilated place or in a fume hood to prevent the accumulation of harmful gases and endanger personal safety. When weighing and transferring, the action should be precise and careful to avoid its spilling or splashing.
Storage should also not be underestimated. It must be placed in a cool, dry place away from ignition and oxidants to prevent deterioration or dangerous reactions.
In addition, chemical properties are also exquisite. When it participates in the reaction, the reaction conditions are strict, and factors such as temperature, pH and reaction time will affect the reaction effect and product purity. Before use, be sure to be familiar with its reaction characteristics and possible side reactions in order to be fully prepared.
At the same time, the waste generated during use should not be discarded at will, and it should be properly disposed of in accordance with relevant regulations to avoid environmental pollution.
In short, when using 1%2C1%27-%5Bchloro%28phenyl%29methanediyl%5Dbis%284-methoxybenzene%29, we must be cautious and strictly abide by safety regulations and operating procedures to ensure safety and smooth progress of experiments or production.
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