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Benzene, 1-(Chlorodiphenylmethyl)-4-Methoxy-
Linshang Chemical
|
HS Code |
217531 |
| Chemical Formula | C16H15ClO |
| Molecular Weight | 258.74 |
| Appearance | Solid (Typical) |
| Odor | Characteristic organic odor (Expected) |
| Melting Point | Varies, data needed for exact value |
| Boiling Point | Varies, data needed for exact value |
| Solubility In Water | Low solubility (Organic nature) |
| Solubility In Organic Solvents | Soluble in common organic solvents (Expected) |
| Density | Data needed for exact value |
| Vapor Pressure | Low (Solid nature, expected) |
| Flash Point | Data needed for exact value |
| Stability | Stable under normal conditions (Expected, without data) |
| Toxicity | Toxicity data needed |
As an accredited Benzene, 1-(Chlorodiphenylmethyl)-4-Methoxy- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1-(chlorodiphenylmethyl)-4 - methoxy - benzene in sealed chemical - grade packaging. |
| Storage | Store "Benzene, 1-(chlorodiphenylmethyl)-4-methoxy-" in a cool, dry, well - ventilated area, away from heat, ignition sources, and incompatible substances. Keep it in a tightly sealed container, preferably made of corrosion - resistant materials. Due to its potential hazards, it should be stored separately from oxidizing agents, acids, and bases to prevent dangerous reactions. |
| Shipping | Shipment of "Benzene, 1-(chlorodiphenylmethyl)-4-methoxy-" must follow strict chemical transport regulations. It should be properly packaged in corrosion - resistant containers, labeled clearly, and shipped via carriers compliant with hazardous chemical shipping laws. |
Competitive Benzene, 1-(Chlorodiphenylmethyl)-4-Methoxy- prices that fit your budget—flexible terms and customized quotes for every order.
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What are the main uses of 1- (chlorodiphenylmethyl) -4 -methoxybenzene?
(1) "1 + - (cyanodiethyl alkyl) - 4 -methoxybenzene", its main uses are as follows:
This compound is used in chemical synthesis, and its use is quite critical. In the field of organic synthesis, it often acts as an important intermediary. With its own special chemical structure, it can participate in a variety of chemical reactions, just like the cornerstone of building a delicate pavilion, laying the foundation for the construction of more complex organic molecular structures.
In the field of pharmaceutical research and development, it also has significance that cannot be ignored. The creation of many new drugs often relies on its participation in reactions to achieve specific molecular structures, which in turn endows drugs with unique pharmacological activities. It may help to enhance the affinity of drugs to specific targets, or enhance the metabolic stability of drugs in the body, and contribute to human health and well-being.
In the field of materials science, its use has also been demonstrated. It can be used as a starting material for the synthesis of functional materials, and through a series of chemical reactions, it can endow materials with special properties such as optics and electricity. For example, when preparing materials with specific photoelectric conversion properties, they can become an important component in the construction of molecular systems, which is expected to promote the progress and development of optoelectronic devices and other fields.
In conclusion, although "1 + - (cyanodiethyl alkyl) - 4 -methoxybenzene" is an organic compound, it plays an indispensable role in many important fields such as chemical industry, medicine, materials, etc. With its unique chemical properties, it has a potential and far-reaching impact on technological innovation and development in various fields.
This compound is used in chemical synthesis, and its use is quite critical. In the field of organic synthesis, it often acts as an important intermediary. With its own special chemical structure, it can participate in a variety of chemical reactions, just like the cornerstone of building a delicate pavilion, laying the foundation for the construction of more complex organic molecular structures.
In the field of pharmaceutical research and development, it also has significance that cannot be ignored. The creation of many new drugs often relies on its participation in reactions to achieve specific molecular structures, which in turn endows drugs with unique pharmacological activities. It may help to enhance the affinity of drugs to specific targets, or enhance the metabolic stability of drugs in the body, and contribute to human health and well-being.
In the field of materials science, its use has also been demonstrated. It can be used as a starting material for the synthesis of functional materials, and through a series of chemical reactions, it can endow materials with special properties such as optics and electricity. For example, when preparing materials with specific photoelectric conversion properties, they can become an important component in the construction of molecular systems, which is expected to promote the progress and development of optoelectronic devices and other fields.
In conclusion, although "1 + - (cyanodiethyl alkyl) - 4 -methoxybenzene" is an organic compound, it plays an indispensable role in many important fields such as chemical industry, medicine, materials, etc. With its unique chemical properties, it has a potential and far-reaching impact on technological innovation and development in various fields.
What are the physical properties of 1- (chlorodiphenylmethyl) -4 -methoxybenzene
(1) On the Physical Properties of Hydroxyethyl and Methoxyphenyl
Husband (1) plus (hydroxyethyl) minus tetramethoxyphenyl, each of which has its own unique physical properties.
Hydroxyethyl, hydrophilic. Due to the presence of hydroxyl groups, it is easy to form hydrogen bonds with water. It is like an alcohol, and its hydroxyl groups can attract water molecules, so hydroxyethyl groups often make the compounds in which it is located have a certain solubility in water. And hydroxyl groups have active chemical activity and can participate in many reactions, such as esterification reactions, and react with acids to form esters. In its spatial structure, the electronegativity of the oxygen atom is strong, causing the electron cloud to be biased towards it, causing the hydroxyl group to have polarity. This polarity affects the intermolecular force of the compound, which in turn affects its boiling point and melting point. Usually, compounds containing hydroxyethyl groups have higher boiling points. In addition to van der Waals forces between molecules, the action of hydrogen bonds also increases the intermolecular binding force.
In methoxy phenyl groups, methoxy groups have a electron supply effect. Phenyl groups are conjugated systems, and the oxygen atoms of methoxy groups have lone pairs of electrons, which can be conjugated with the π electrons of phenyl groups, increasing the electron cloud density of the phenyl ring. This electronic effect affects the chemical activity and physical properties of the compound. In terms of physical properties, it affects its solubility. Due to the combination of methoxy and phenyl groups, the compound has a certain lipid solubility and can be soluble in some organic solvents. However, its overall solubility varies depending on the relative position of methoxy and benzene rings. And the planar structure of phenyl groups imparts a certain rigidity to the compound, which affects its molecular stacking mode and has an effect on melting point and crystal form.
Furthermore, in the mixture, hydroxyethyl interacts with methoxyphenyl. The functional groups of the two may have weak interactions, such as van der Waals force, hydrogen bond (if conditions are suitable), which affect the phase state and rheological properties of the mixture.
In summary, hydroxyethyl and methoxyphenyl each exhibit unique physical properties due to their functional groups and structural characteristics, and interact with each other when coexisting, which is of great significance in the fields of chemical industry and materials.
Husband (1) plus (hydroxyethyl) minus tetramethoxyphenyl, each of which has its own unique physical properties.
Hydroxyethyl, hydrophilic. Due to the presence of hydroxyl groups, it is easy to form hydrogen bonds with water. It is like an alcohol, and its hydroxyl groups can attract water molecules, so hydroxyethyl groups often make the compounds in which it is located have a certain solubility in water. And hydroxyl groups have active chemical activity and can participate in many reactions, such as esterification reactions, and react with acids to form esters. In its spatial structure, the electronegativity of the oxygen atom is strong, causing the electron cloud to be biased towards it, causing the hydroxyl group to have polarity. This polarity affects the intermolecular force of the compound, which in turn affects its boiling point and melting point. Usually, compounds containing hydroxyethyl groups have higher boiling points. In addition to van der Waals forces between molecules, the action of hydrogen bonds also increases the intermolecular binding force.
In methoxy phenyl groups, methoxy groups have a electron supply effect. Phenyl groups are conjugated systems, and the oxygen atoms of methoxy groups have lone pairs of electrons, which can be conjugated with the π electrons of phenyl groups, increasing the electron cloud density of the phenyl ring. This electronic effect affects the chemical activity and physical properties of the compound. In terms of physical properties, it affects its solubility. Due to the combination of methoxy and phenyl groups, the compound has a certain lipid solubility and can be soluble in some organic solvents. However, its overall solubility varies depending on the relative position of methoxy and benzene rings. And the planar structure of phenyl groups imparts a certain rigidity to the compound, which affects its molecular stacking mode and has an effect on melting point and crystal form.
Furthermore, in the mixture, hydroxyethyl interacts with methoxyphenyl. The functional groups of the two may have weak interactions, such as van der Waals force, hydrogen bond (if conditions are suitable), which affect the phase state and rheological properties of the mixture.
In summary, hydroxyethyl and methoxyphenyl each exhibit unique physical properties due to their functional groups and structural characteristics, and interact with each other when coexisting, which is of great significance in the fields of chemical industry and materials.
What are the chemical properties of 1- (chlorodiphenylmethyl) -4 -methoxybenzene
(Monochlorodifluoromethyl) -1-4-methoxybenzene, which is an organic compound. Its chemical properties are as follows:
First of all, it contains fluorine atoms. Due to the high electronegativity of fluorine atoms, it will significantly affect the distribution of molecular electron clouds, resulting in the compound exhibiting unique chemical activity. It is relatively stable, and the fluorine atom makes the C-F bond more energetic. Under many common chemical reaction conditions, this bond is not easy to break.
Furthermore, the presence of methoxy groups also affects the properties of compounds. Methoxy groups are the power supply groups, which can enhance the electron cloud density of the benzene ring, making the benzene ring more prone to electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. For example, under appropriate conditions, when interacting with halogenating reagents, halogen atoms can be introduced at specific positions in the benzene ring.
In addition, chlorine atoms in (monochlorodifluoromethyl) have certain reactivity. Under the action of specific nucleophiles, chlorine atoms can be replaced to form new compounds. For example, when reacting with nucleophiles such as sodium alcohol, chlorine atoms will be replaced by alkoxy groups.
Moreover, this compound may participate in coupling reactions in organic synthesis. With the characteristics of benzene rings and (monochlorodifluoromethyl), under the action of suitable catalysts, it can be coupled with other organic halides or organometallic reagents to realize the construction of carbon-carbon bonds or carbon-heteroatom bonds, providing a way for the synthesis of more complex organic compounds.
The chemical properties of this compound make it potentially valuable in the fields of organic synthesis, medicinal chemistry, etc., and can be used as a key intermediate to create various functional organic materials or drug molecules.
First of all, it contains fluorine atoms. Due to the high electronegativity of fluorine atoms, it will significantly affect the distribution of molecular electron clouds, resulting in the compound exhibiting unique chemical activity. It is relatively stable, and the fluorine atom makes the C-F bond more energetic. Under many common chemical reaction conditions, this bond is not easy to break.
Furthermore, the presence of methoxy groups also affects the properties of compounds. Methoxy groups are the power supply groups, which can enhance the electron cloud density of the benzene ring, making the benzene ring more prone to electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. For example, under appropriate conditions, when interacting with halogenating reagents, halogen atoms can be introduced at specific positions in the benzene ring.
In addition, chlorine atoms in (monochlorodifluoromethyl) have certain reactivity. Under the action of specific nucleophiles, chlorine atoms can be replaced to form new compounds. For example, when reacting with nucleophiles such as sodium alcohol, chlorine atoms will be replaced by alkoxy groups.
Moreover, this compound may participate in coupling reactions in organic synthesis. With the characteristics of benzene rings and (monochlorodifluoromethyl), under the action of suitable catalysts, it can be coupled with other organic halides or organometallic reagents to realize the construction of carbon-carbon bonds or carbon-heteroatom bonds, providing a way for the synthesis of more complex organic compounds.
The chemical properties of this compound make it potentially valuable in the fields of organic synthesis, medicinal chemistry, etc., and can be used as a key intermediate to create various functional organic materials or drug molecules.
What are the applications of 1- (chlorodiphenylmethyl) - 4 -methoxybenzene in synthesis?
1 + - (cyanodiethyl alkyl) - 4 -methoxybenzyl has many uses in synthesis.
This cyanodiethyl alkyl and methoxybenzyl related substances play an extraordinary role in the synthesis of medicine. When creating drugs for the treatment of cardiovascular diseases, 1 + - (cyanodiethyl alkyl) - 4 -methoxybenzyl can act as a key intermediate. Its unique chemical structure can be precisely combined with other compounds through a series of delicate chemical reactions to shape a molecular structure with specific pharmacological activities. By adjusting its substituents, the lipophilicity, water solubility and affinity with the target can be fine-tuned to improve the efficacy of the drug and reduce the toxic and side effects.
In the field of materials science, both are also useful. 1 + - (cyanodiethyl alkyl) - 4 -methoxybenzyl can participate in the synthesis of high-performance polymers. By introducing it into the main or side chains of the polymer, it can impart unique electrical, optical or mechanical properties to the polymer. For example, polymer materials with special fluorescent properties can be prepared, which can be used in optical sensors, Light Emitting Diodes, etc.; or to enhance the heat resistance and chemical stability of polymers, expanding their application scope in extreme environments.
In the field of organic synthetic chemistry, 1 + - (cyanodiethyl alkyl) - 4 -methoxybenzyl is like a cornerstone. Due to the activity check point in its structure, it can trigger various classical organic reactions, such as nucleophilic substitution, electrophilic addition, oxidation reduction, etc. Chemists can use it as a starting material to build complex and diverse organic compounds by ingeniously designing reaction paths, providing a rich material basis for new drug development and material innovation.
This cyanodiethyl alkyl and methoxybenzyl related substances play an extraordinary role in the synthesis of medicine. When creating drugs for the treatment of cardiovascular diseases, 1 + - (cyanodiethyl alkyl) - 4 -methoxybenzyl can act as a key intermediate. Its unique chemical structure can be precisely combined with other compounds through a series of delicate chemical reactions to shape a molecular structure with specific pharmacological activities. By adjusting its substituents, the lipophilicity, water solubility and affinity with the target can be fine-tuned to improve the efficacy of the drug and reduce the toxic and side effects.
In the field of materials science, both are also useful. 1 + - (cyanodiethyl alkyl) - 4 -methoxybenzyl can participate in the synthesis of high-performance polymers. By introducing it into the main or side chains of the polymer, it can impart unique electrical, optical or mechanical properties to the polymer. For example, polymer materials with special fluorescent properties can be prepared, which can be used in optical sensors, Light Emitting Diodes, etc.; or to enhance the heat resistance and chemical stability of polymers, expanding their application scope in extreme environments.
In the field of organic synthetic chemistry, 1 + - (cyanodiethyl alkyl) - 4 -methoxybenzyl is like a cornerstone. Due to the activity check point in its structure, it can trigger various classical organic reactions, such as nucleophilic substitution, electrophilic addition, oxidation reduction, etc. Chemists can use it as a starting material to build complex and diverse organic compounds by ingeniously designing reaction paths, providing a rich material basis for new drug development and material innovation.
What is the preparation method of 1- (chlorodiphenylmethyl) - 4 -methoxybenzene?
To prepare (cyanodiethyl alkyl) and 1 - (cyanodiethyl alkyl) - 4 - methoxybenzene, the method is as follows:
First take an appropriate amount of raw materials, such as compounds containing ethyl groups, and after fine treatment, make them meet cyanide in a specific reactor. The environment in the kettle needs to be precisely controlled, and the temperature should be maintained in a certain range. This range is determined by repeated tests, which is about XX degrees Celsius to XX degrees Celsius. At the same time, the pressure must also be stable at the corresponding value to ensure that the reaction can proceed in the expected direction. When
reacting, an appropriate catalyst needs to be added. The choice of this catalyst is very critical, depending on the rate of the reaction and the purity of the product. The dosage also needs to be accurately weighed, and too much or too little can cause the reaction deviation.
After the initial formation of (cyanodiethylalkyl), it is mixed with the raw materials required for the preparation of methoxybenzene. This mixing process also needs to be carefully added in a specific ratio. Then the reaction is carried out under another reaction condition, which has different settings in terms of temperature, pressure and catalyst. The temperature may rise to XX degrees Celsius, and the pressure is adjusted accordingly. The catalyst may be changed to another category, or the dosage may be fine-tuned on the basis of the original catalyst.
During this period, it is necessary to closely monitor the reaction process, and rely on various delicate instruments, such as spectrometers, to gain insight into the formation of products and the amount of impurities in the reaction. In case of abnormalities, adjust the reaction parameters immediately.
After many complex processes such as reaction, separation, and purification, pure 1- (cyanodiethyl alkyl) -4-methoxybenzene and (cyanodiethyl alkyl) can be obtained. Each step requires fine operation, and it is difficult to achieve the expected product quality and yield due to slight errors.
First take an appropriate amount of raw materials, such as compounds containing ethyl groups, and after fine treatment, make them meet cyanide in a specific reactor. The environment in the kettle needs to be precisely controlled, and the temperature should be maintained in a certain range. This range is determined by repeated tests, which is about XX degrees Celsius to XX degrees Celsius. At the same time, the pressure must also be stable at the corresponding value to ensure that the reaction can proceed in the expected direction. When
reacting, an appropriate catalyst needs to be added. The choice of this catalyst is very critical, depending on the rate of the reaction and the purity of the product. The dosage also needs to be accurately weighed, and too much or too little can cause the reaction deviation.
After the initial formation of (cyanodiethylalkyl), it is mixed with the raw materials required for the preparation of methoxybenzene. This mixing process also needs to be carefully added in a specific ratio. Then the reaction is carried out under another reaction condition, which has different settings in terms of temperature, pressure and catalyst. The temperature may rise to XX degrees Celsius, and the pressure is adjusted accordingly. The catalyst may be changed to another category, or the dosage may be fine-tuned on the basis of the original catalyst.
During this period, it is necessary to closely monitor the reaction process, and rely on various delicate instruments, such as spectrometers, to gain insight into the formation of products and the amount of impurities in the reaction. In case of abnormalities, adjust the reaction parameters immediately.
After many complex processes such as reaction, separation, and purification, pure 1- (cyanodiethyl alkyl) -4-methoxybenzene and (cyanodiethyl alkyl) can be obtained. Each step requires fine operation, and it is difficult to achieve the expected product quality and yield due to slight errors.
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