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1-(Chloromethyl)-2-[(2-Methylphenoxy)Methyl]Benzene
Linshang Chemical
|
HS Code |
739305 |
| Chemical Formula | C15H15ClO |
| Molecular Weight | 246.73 |
| Appearance | Typically a colorless to light - yellow liquid (description may vary) |
| Boiling Point | Estimated around 320 - 330 °C (approximate, may vary based on purity and conditions) |
| Density | Approximately 1.1 g/cm³ (estimated, subject to variation) |
| Solubility In Water | Insoluble in water |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether, chloroform |
| Flash Point | Relatively high, estimated around 120 - 130 °C (approximate) |
| Vapor Pressure | Low vapor pressure at room temperature |
As an accredited 1-(Chloromethyl)-2-[(2-Methylphenoxy)Methyl]Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 - (Chloromethyl)-2 - [(2 - methylphenoxy)methyl]benzene in 500g sealed chemical - grade bottles. |
| Storage | 1-(Chloromethyl)-2-[(2 - methylphenoxy)methyl]benzene should be stored in a cool, dry, well - ventilated area. Keep it away from heat sources, open flames, and oxidizing agents. Store in a tightly sealed container to prevent leakage and exposure to air or moisture, which could potentially lead to chemical reactions or degradation. |
| Shipping | 1-(Chloromethyl)-2-[(2 - methylphenoxy)methyl]benzene is shipped in accordance with strict chemical regulations. Packed in suitable containers, it's transported by specialized carriers, ensuring safety during transit. |
Competitive 1-(Chloromethyl)-2-[(2-Methylphenoxy)Methyl]Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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What is the use of 1- (chloromethyl) -2- [ (2-methylphenoxy) methyl] benzene?
1-% (cyanomethyl) -2- [ (2-methylphenoxymethyl) phenyl] benzene, this compound has important uses in many fields.
In the field of medicinal chemistry, as a key intermediate, it is of great significance for the development of new drugs. Taking drugs for the treatment of specific diseases as an example, through the modification and modification of its chemical structure, drug molecules with high activity, high selectivity and low toxicity and side effects can be obtained. Due to its unique chemical structure and activity, it can precisely act on disease-related targets and provide effective means for disease treatment.
In the field of materials science, this compound can participate in the preparation of high-performance materials. Such as the preparation of materials with special optical, electrical or mechanical properties, in the field of organic optoelectronic materials, it can be used as a core structural unit, endowing the material with excellent properties such as light absorption and charge transport, and used in the manufacture of high-efficiency organic Light Emitting Diodes, solar cells and other optoelectronic devices.
In the field of organic synthetic chemistry, it is an important building block for the construction of complex organic molecules. With the different activity check points in its structure, chemists can use a variety of organic reactions, such as nucleophilic substitution, coupling reactions, etc., to connect it with other organic molecules, build organic compounds with diverse structures and functions, expand the field of organic synthetic chemistry research, and help the discovery and synthesis of new organic compounds.
In the field of medicinal chemistry, as a key intermediate, it is of great significance for the development of new drugs. Taking drugs for the treatment of specific diseases as an example, through the modification and modification of its chemical structure, drug molecules with high activity, high selectivity and low toxicity and side effects can be obtained. Due to its unique chemical structure and activity, it can precisely act on disease-related targets and provide effective means for disease treatment.
In the field of materials science, this compound can participate in the preparation of high-performance materials. Such as the preparation of materials with special optical, electrical or mechanical properties, in the field of organic optoelectronic materials, it can be used as a core structural unit, endowing the material with excellent properties such as light absorption and charge transport, and used in the manufacture of high-efficiency organic Light Emitting Diodes, solar cells and other optoelectronic devices.
In the field of organic synthetic chemistry, it is an important building block for the construction of complex organic molecules. With the different activity check points in its structure, chemists can use a variety of organic reactions, such as nucleophilic substitution, coupling reactions, etc., to connect it with other organic molecules, build organic compounds with diverse structures and functions, expand the field of organic synthetic chemistry research, and help the discovery and synthesis of new organic compounds.
What are the physical properties of 1- (chloromethyl) -2- [ (2-methylphenoxy) methyl] benzene?
(1) This physical property is quite complicated, and I will come one by one.
(2) First, about (cyanomethyl), this group has special activity. In its structure, the cyanyl group is connected to the methyl group, and the carbon and nitrogen triple bond of the cyanyl group is active in nature and electron-rich cloud density. It is often used in many reactions as a nucleophilic reagent and is easy to interact with electron-deficient systems. And the cyanyl group has an electron-absorbing effect, which can affect the activity of hydrogen atoms on the methyl group, resulting in its unique chemical properties and can participate in various reactions such as substitution and addition.
(3) Second, for [ (2-acetoxyacetyl) methyl] ethers, its structure is more complicated. Acetoxy acetyl moiety, in acetoxy, the carbonyl group conjugates with the oxygen atom, which reduces the electron cloud density of the oxygen atom, and the electron-giving effect of the acetyl group has a certain influence. After this part is connected to the methyl group, it is connected to the ether bond. The oxygen atom of the ether bond has a solitary pair of electrons and has a certain nucleophilicity, but its activity also changes due to the influence of surrounding groups. Overall, the substance exhibits special physical and chemical properties due to the interaction of various groups. From the perspective of physical properties, because it contains polar groups and non-polar parts, it has a certain solubility in organic solvents. And intermolecular forces, including van der Waals forces, dipole-dipole forces, etc., affect its melting point, boiling point and other physical parameters. Chemically, various groups cooperate to enable them to participate in reactions such as hydrolysis and esterification. They are often important intermediates in the field of organic synthesis and play a key role in drug synthesis and material preparation.
(2) First, about (cyanomethyl), this group has special activity. In its structure, the cyanyl group is connected to the methyl group, and the carbon and nitrogen triple bond of the cyanyl group is active in nature and electron-rich cloud density. It is often used in many reactions as a nucleophilic reagent and is easy to interact with electron-deficient systems. And the cyanyl group has an electron-absorbing effect, which can affect the activity of hydrogen atoms on the methyl group, resulting in its unique chemical properties and can participate in various reactions such as substitution and addition.
(3) Second, for [ (2-acetoxyacetyl) methyl] ethers, its structure is more complicated. Acetoxy acetyl moiety, in acetoxy, the carbonyl group conjugates with the oxygen atom, which reduces the electron cloud density of the oxygen atom, and the electron-giving effect of the acetyl group has a certain influence. After this part is connected to the methyl group, it is connected to the ether bond. The oxygen atom of the ether bond has a solitary pair of electrons and has a certain nucleophilicity, but its activity also changes due to the influence of surrounding groups. Overall, the substance exhibits special physical and chemical properties due to the interaction of various groups. From the perspective of physical properties, because it contains polar groups and non-polar parts, it has a certain solubility in organic solvents. And intermolecular forces, including van der Waals forces, dipole-dipole forces, etc., affect its melting point, boiling point and other physical parameters. Chemically, various groups cooperate to enable them to participate in reactions such as hydrolysis and esterification. They are often important intermediates in the field of organic synthesis and play a key role in drug synthesis and material preparation.
What are the chemical properties of 1- (chloromethyl) -2- [ (2-methylphenoxy) methyl] benzene
1 - (cyanomethyl) - 2 - [ (2 - methylphenoxymethyl) phenyl] benzene, the detailed physical properties are related to the category of organic chemistry. It has certain physical and chemical characteristics.
In terms of its physical properties, at room temperature, it is mostly in a solid state due to its intermolecular forces and structure. Melting point and boiling point are key indicators of physical state changes, but the exact value needs to be tested experimentally, because it is affected by various groups in the molecular structure. Within the molecule, the benzene ring structure gives it a certain rigidity, and the substituents such as methyl, cyanomethyl and phenoxymethyl have the effect of regulating the interaction between molecules, which in turn affects the melting boiling point.
As for the solubility, according to the principle of similar miscibility, because the molecule is rich in aromatic rings, it is the non-polar part dominant, and it should have good solubility in non-polar organic solvents, such as toluene and dichloromethane; in polar solvents, such as water, the solubility is poor, and the cover water is a strong polar solvent, which does not match the force between the organic molecules.
Its chemical properties, the presence of the benzene ring makes it aromatic, and electrophilic substitution reactions can occur. In case of electrophilic reagents, hydrogen atoms on the benzene ring can be replaced. Because the methyl group is the power supply group, the electron cloud density of the benzene ring can be increased, making the electrophilic substitution reactions more likely to occur in the adjacent and para-position. The cyanyl group in cyanomethyl has strong electron-absorbing properties. Although it is far away from the benzene ring, it also has an impact on the distribution of molecular electron clouds.
The phenoxy group of the benzene part, the oxygen atom has lone pair electrons, and can participate in chemical reactions, such as interacting with electrophilic reagents, or under appropriate conditions, ether bond cleavage reactions. Overall, 1 - (cyanomethyl) - 2 - [ (2 - methylphenoxymethyl) phenyl] benzene has a complex structure and contains a variety of chemical reaction activity check points, which may have specific uses and values in the field of organic synthesis.
In terms of its physical properties, at room temperature, it is mostly in a solid state due to its intermolecular forces and structure. Melting point and boiling point are key indicators of physical state changes, but the exact value needs to be tested experimentally, because it is affected by various groups in the molecular structure. Within the molecule, the benzene ring structure gives it a certain rigidity, and the substituents such as methyl, cyanomethyl and phenoxymethyl have the effect of regulating the interaction between molecules, which in turn affects the melting boiling point.
As for the solubility, according to the principle of similar miscibility, because the molecule is rich in aromatic rings, it is the non-polar part dominant, and it should have good solubility in non-polar organic solvents, such as toluene and dichloromethane; in polar solvents, such as water, the solubility is poor, and the cover water is a strong polar solvent, which does not match the force between the organic molecules.
Its chemical properties, the presence of the benzene ring makes it aromatic, and electrophilic substitution reactions can occur. In case of electrophilic reagents, hydrogen atoms on the benzene ring can be replaced. Because the methyl group is the power supply group, the electron cloud density of the benzene ring can be increased, making the electrophilic substitution reactions more likely to occur in the adjacent and para-position. The cyanyl group in cyanomethyl has strong electron-absorbing properties. Although it is far away from the benzene ring, it also has an impact on the distribution of molecular electron clouds.
The phenoxy group of the benzene part, the oxygen atom has lone pair electrons, and can participate in chemical reactions, such as interacting with electrophilic reagents, or under appropriate conditions, ether bond cleavage reactions. Overall, 1 - (cyanomethyl) - 2 - [ (2 - methylphenoxymethyl) phenyl] benzene has a complex structure and contains a variety of chemical reaction activity check points, which may have specific uses and values in the field of organic synthesis.
What are the synthesis methods of 1- (chloromethyl) -2- [ (2-methylphenoxy) methyl] benzene?
To prepare 1 - (cyanomethyl) - 2 - [ (2 - methylphenoxymethyl) phenyl] benzene, there are many methods for its synthesis, which are described below.
First, it can be started from the corresponding halogenate. First, a suitable halogenated benzyl is reacted with sodium cyanide, and a cyanomethyl derivative is prepared by nucleophilic substitution. In this step, attention should be paid to the control of the reaction conditions, such as the choice of solvent and the regulation of temperature, in order to improve the yield. Then the obtained cyanomethyl compound is reacted with a specific phenol under alkaline conditions to complete the construction of ether bonds, and then the synthesis of the target is completed through subsequent steps.
Second, an aldehyde and ketone compound is used as a raw material. The cyanoalcohol is formed by the reaction of aldol and ketone with cyanide reagent, and the cyanide-containing methyl structure is appropriately converted. Then it reacts with benzene ring derivatives through condensation to gradually build the skeleton of the target molecule. In this path, the activity regulation of carbonyl compounds is involved to ensure that the reaction proceeds in the expected direction.
Third, the strategy of metal catalysis is used. For example, the coupling reaction catalyzed by palladium, the different halogenated aromatics, alkenyl halides and other substrates are coupled under the action of palladium catalyst and ligand. The connection between the benzene rings can be constructed first, and then the substituents such as cyanomethyl and phenoxy methyl are introduced. This method requires high activity and selectivity of the catalyst, and requires careful screening and optimization. In the
synthesis process, the purity of raw materials, the precise control of reaction conditions, and the effective separation and purification of intermediates are all key factors affecting the yield and purity of the product. Experimenters need to adjust and optimize flexibly according to the actual situation to achieve the best synthesis effect.
First, it can be started from the corresponding halogenate. First, a suitable halogenated benzyl is reacted with sodium cyanide, and a cyanomethyl derivative is prepared by nucleophilic substitution. In this step, attention should be paid to the control of the reaction conditions, such as the choice of solvent and the regulation of temperature, in order to improve the yield. Then the obtained cyanomethyl compound is reacted with a specific phenol under alkaline conditions to complete the construction of ether bonds, and then the synthesis of the target is completed through subsequent steps.
Second, an aldehyde and ketone compound is used as a raw material. The cyanoalcohol is formed by the reaction of aldol and ketone with cyanide reagent, and the cyanide-containing methyl structure is appropriately converted. Then it reacts with benzene ring derivatives through condensation to gradually build the skeleton of the target molecule. In this path, the activity regulation of carbonyl compounds is involved to ensure that the reaction proceeds in the expected direction.
Third, the strategy of metal catalysis is used. For example, the coupling reaction catalyzed by palladium, the different halogenated aromatics, alkenyl halides and other substrates are coupled under the action of palladium catalyst and ligand. The connection between the benzene rings can be constructed first, and then the substituents such as cyanomethyl and phenoxy methyl are introduced. This method requires high activity and selectivity of the catalyst, and requires careful screening and optimization. In the
synthesis process, the purity of raw materials, the precise control of reaction conditions, and the effective separation and purification of intermediates are all key factors affecting the yield and purity of the product. Experimenters need to adjust and optimize flexibly according to the actual situation to achieve the best synthesis effect.
What are the precautions for 1- (chloromethyl) -2- [ (2-methylphenoxy) methyl] benzene during storage and transportation?
When storing and transporting (1 - (cyanomethyl) - 2 - [ (2 - methylphenoxy methyl) phenyl] ether, there are many key points to be paid attention to.
First of all, because of its specific chemical properties, the storage environment is strict. It should be placed in a cool, dry and well-ventilated place, away from fires and heat sources. This substance may cause combustion and explosion in case of open flames and hot topics, so fireworks must be strictly prohibited in the storage place. And it needs to be stored separately from oxidants, acids, bases, etc., and must not be mixed to prevent violent chemical reactions.
The transportation process should also not be taken lightly. Make sure the packaging is complete and the loading is secure. Transportation vehicles should be equipped with the appropriate variety and quantity of fire-fighting equipment and leakage emergency treatment equipment. During driving, it should be protected from exposure to the sun, rain and high temperature. During road transportation, it should be driven according to the specified route, and do not stop in residential areas and densely populated areas. If a leak occurs during transportation, personnel in the leaked contaminated area should be quickly evacuated to a safe area and quarantined, and access should be strictly restricted. Emergency personnel should wear self-contained positive pressure breathing apparatus, wear anti-toxic clothing, and cut off the source of leakage as much as possible. For small leaks, it can be absorbed by sand, vermiculite or other inert materials; when a large number of leaks occur, it is necessary to build a dike or dig a pit for containment, cover it with foam, reduce steam disasters, and then transfer it to a tank car or a special collector for recycling or transportation to a waste treatment site for disposal.
In conclusion, whether it is the storage or transportation of this chemical, relevant safety procedures must be strictly followed to ensure the safety of personnel and the environment.
First of all, because of its specific chemical properties, the storage environment is strict. It should be placed in a cool, dry and well-ventilated place, away from fires and heat sources. This substance may cause combustion and explosion in case of open flames and hot topics, so fireworks must be strictly prohibited in the storage place. And it needs to be stored separately from oxidants, acids, bases, etc., and must not be mixed to prevent violent chemical reactions.
The transportation process should also not be taken lightly. Make sure the packaging is complete and the loading is secure. Transportation vehicles should be equipped with the appropriate variety and quantity of fire-fighting equipment and leakage emergency treatment equipment. During driving, it should be protected from exposure to the sun, rain and high temperature. During road transportation, it should be driven according to the specified route, and do not stop in residential areas and densely populated areas. If a leak occurs during transportation, personnel in the leaked contaminated area should be quickly evacuated to a safe area and quarantined, and access should be strictly restricted. Emergency personnel should wear self-contained positive pressure breathing apparatus, wear anti-toxic clothing, and cut off the source of leakage as much as possible. For small leaks, it can be absorbed by sand, vermiculite or other inert materials; when a large number of leaks occur, it is necessary to build a dike or dig a pit for containment, cover it with foam, reduce steam disasters, and then transfer it to a tank car or a special collector for recycling or transportation to a waste treatment site for disposal.
In conclusion, whether it is the storage or transportation of this chemical, relevant safety procedures must be strictly followed to ensure the safety of personnel and the environment.
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