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1(-Chlorophenyl-Methyl)-2-Mehtylbenzene
Linshang Chemical
|
HS Code |
461243 |
| Chemical Formula | C14H13Cl |
| Molar Mass | 216.706 g/mol |
| Appearance | Typically a colorless to light - yellow liquid (assumed based on similar aromatic compounds) |
| Boiling Point | Estimated around 300 - 320 °C (aromatic hydrocarbons with similar structures) |
| Density | Approximately 1.1 - 1.2 g/cm³ (comparable to related aromatic compounds) |
| Solubility In Water | Insoluble (aromatic hydrocarbons are generally hydrophobic) |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone, and benzene |
| Vapor Pressure | Low vapor pressure at room temperature (aromatic hydrocarbons with high molecular weight) |
| Flash Point | Estimated around 100 - 120 °C (flammability hazard similar to related aromatic derivatives) |
As an accredited 1(-Chlorophenyl-Methyl)-2-Mehtylbenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 1 kg of (chlorophenyl - methyl)-2 - methylbenzene in a sealed, chemical - resistant drum. |
| Storage | 1-(Chlorophenyl - methyl)-2 - methylbenzene should be stored in a cool, dry, well - ventilated area, away from heat sources and ignition points as it may be flammable. Keep it in a tightly - sealed container to prevent vapor leakage. Store it separately from oxidizing agents and incompatible substances to avoid potential reactions. Label the storage container clearly with its name and relevant safety information. |
| Shipping | The chemical 1-(chlorophenyl - methyl)-2 - methylbenzene should be shipped in sealed, corrosion - resistant containers. Follow strict hazardous material shipping regulations, ensuring proper labeling and documentation for safe transport. |
Competitive 1(-Chlorophenyl-Methyl)-2-Mehtylbenzene prices that fit your budget—flexible terms and customized quotes for every order.
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What are the physical properties of 1- (chlorophenyl-methyl) -2-methylbenzene?
(1) On (cyano-methyl)
(cyano-methyl), it is an important structural fragment in organic chemistry. Cyano, characterized by carbon-nitrogen triple bonds, has strong electronegativity and chemical activity; methyl is a group containing one carbon atom and three hydrogen atoms, and its properties are relatively stable. The combination of the two forms (cyano-methyl), which has the characteristics of both, and is of great significance in many fields such as organic synthesis. Its chemical activity is derived from the unsaturation of cyano groups, which can trigger a variety of chemical reactions, such as nucleophilic substitution, addition, etc., providing the possibility to construct complex organic molecular structures.
(II) Physical Properties of Methylnitrile
Methylnitrile, also known as acetonitrile, is a common organic compound. Its color is clear and transparent, like water, and has a special smell. Although it is not strong and pungent, it can also be perceived by people. In terms of boiling point, it is about 81.6 ° C. At this temperature, methylnitrile converts from liquid to gaseous state. Its melting point is -45.7 ° C. Below this temperature, it condenses into a solid state.
Methylnitrile has a certain solubility in water, and can form hydrogen bonds with water, so it can be miscible with water in a certain proportion. At the same time, it is also an excellent organic solvent, which has good solubility for many organic compounds, such as common hydrocarbons, alcohols, ethers and other substances. This property makes it often used as a reaction medium in organic synthesis experiments and industrial production to facilitate the smooth progress of chemical reactions.
Furthermore, the density of methylnitrile is slightly smaller than that of water, about 0.786 g/cm ³. In the stratification experiment, if mixed with water, methylnitrile will float on water. Its refractive index also has a specific value, around 1.3441. This physical constant has important reference value for the identification and analysis of methylnitrile. The physical properties of methylnitrile enable it to occupy a place in the field of chemistry and play a key role in organic synthesis, separation and purification. It is an indispensable substance for organic chemistry research and related industrial production.
(cyano-methyl), it is an important structural fragment in organic chemistry. Cyano, characterized by carbon-nitrogen triple bonds, has strong electronegativity and chemical activity; methyl is a group containing one carbon atom and three hydrogen atoms, and its properties are relatively stable. The combination of the two forms (cyano-methyl), which has the characteristics of both, and is of great significance in many fields such as organic synthesis. Its chemical activity is derived from the unsaturation of cyano groups, which can trigger a variety of chemical reactions, such as nucleophilic substitution, addition, etc., providing the possibility to construct complex organic molecular structures.
(II) Physical Properties of Methylnitrile
Methylnitrile, also known as acetonitrile, is a common organic compound. Its color is clear and transparent, like water, and has a special smell. Although it is not strong and pungent, it can also be perceived by people. In terms of boiling point, it is about 81.6 ° C. At this temperature, methylnitrile converts from liquid to gaseous state. Its melting point is -45.7 ° C. Below this temperature, it condenses into a solid state.
Methylnitrile has a certain solubility in water, and can form hydrogen bonds with water, so it can be miscible with water in a certain proportion. At the same time, it is also an excellent organic solvent, which has good solubility for many organic compounds, such as common hydrocarbons, alcohols, ethers and other substances. This property makes it often used as a reaction medium in organic synthesis experiments and industrial production to facilitate the smooth progress of chemical reactions.
Furthermore, the density of methylnitrile is slightly smaller than that of water, about 0.786 g/cm ³. In the stratification experiment, if mixed with water, methylnitrile will float on water. Its refractive index also has a specific value, around 1.3441. This physical constant has important reference value for the identification and analysis of methylnitrile. The physical properties of methylnitrile enable it to occupy a place in the field of chemistry and play a key role in organic synthesis, separation and purification. It is an indispensable substance for organic chemistry research and related industrial production.
What are the chemical properties of 1- (chlorophenyl-methyl) -2-methylbenzene?
Alkophenyl-methyl is a common group combination in organic chemistry. Alkophenyl, which is formed by linking an alkyl group to a phenyl group, has both the properties of an alkyl group and the chemical properties of a phenyl group; methyl is a group containing only one carbon atom and three hydrogen atoms.
The chemical properties of methyl benzene are quite rich. It is flammable and burns in sufficient oxygen to form carbon dioxide and water, which is a common oxidation reaction of organic compounds. The reaction equation can be expressed as: $C_7H_8 + 9O_2\ stackrel {ignited }{=\!=\!=} 7CO_2 + 4H_2O $.
In methyl benzene, due to the presence of methyl, the electron cloud distribution of the benzene ring is affected, making the benzene ring more prone to electrophilic substitution. If under the action of appropriate catalysts, it can react with halogens, nitric acid and other electrophilic reagents. Taking the bromide reaction as an example, under the catalysis of iron bromide, methyl benzene reacts with bromide to mainly generate o-bromotoluene and p-bromotoluene. This is because methyl is an o-and para-site locator, so that the electron cloud density of the benzene ring is relatively high, and the electrophilic reagents are more likely to attack these two positions.
In addition, methyl is affected by the benzene ring, and its α-atom hydrogen has a certain activity, For example, under the action of strong oxidants, methyl groups can be oxidized to carboxyl groups to form benzoic acid.
Methylbenzene has important uses in organic synthesis, medicine, fragrances and many other fields due to its unique chemical properties. It is also an indispensable compound in organic chemistry research and industrial production.
The chemical properties of methyl benzene are quite rich. It is flammable and burns in sufficient oxygen to form carbon dioxide and water, which is a common oxidation reaction of organic compounds. The reaction equation can be expressed as: $C_7H_8 + 9O_2\ stackrel {ignited }{=\!=\!=} 7CO_2 + 4H_2O $.
In methyl benzene, due to the presence of methyl, the electron cloud distribution of the benzene ring is affected, making the benzene ring more prone to electrophilic substitution. If under the action of appropriate catalysts, it can react with halogens, nitric acid and other electrophilic reagents. Taking the bromide reaction as an example, under the catalysis of iron bromide, methyl benzene reacts with bromide to mainly generate o-bromotoluene and p-bromotoluene. This is because methyl is an o-and para-site locator, so that the electron cloud density of the benzene ring is relatively high, and the electrophilic reagents are more likely to attack these two positions.
In addition, methyl is affected by the benzene ring, and its α-atom hydrogen has a certain activity, For example, under the action of strong oxidants, methyl groups can be oxidized to carboxyl groups to form benzoic acid.
Methylbenzene has important uses in organic synthesis, medicine, fragrances and many other fields due to its unique chemical properties. It is also an indispensable compound in organic chemistry research and industrial production.
What are the main uses of 1- (chlorophenyl-methyl) -2-methylbenzene?
(1) Halobenzyl-methyl
halobenzyl, that is, benzyl halide, in which benzyl (benzyl) is connected to a halogen atom. Methyl is the simplest alkyl group, composed of only one carbon atom and three hydrogen atoms. The difference between halobenzyl and methyl is significant. Halobenzyl is more active in chemical properties due to the presence of halogen atoms, and can undergo various substitution reactions. Methyl is relatively stable and is often used as a component of organic compounds, which affects the physical and chemical properties of compounds.
Main use of (di) methyl tert-butyl ether
Methyl tert-butyl ether is an important chemical raw material and additive. Its primary use is as a gasoline additive. Adding methyl tert-butyl ether to gasoline can effectively improve the octane number of gasoline, enhance the anti-explosion performance of gasoline, make the engine burn more smoothly, reduce the occurrence of knock, and then improve the power performance and fuel economy of automobiles. At the same time, it can also reduce the emission of carbon monoxide and other pollutants in automobile exhaust, which is beneficial to environmental protection.
Furthermore, methyl tert-butyl ether also has important applications in the field of organic synthesis. Because of its specific chemical structure and reactivity, it can be used as a reaction intermediate to participate in many organic synthesis reactions, and is used in the preparation of various fine chemicals and drugs. In chemical production, it is often used as a solvent because it has good solubility, can dissolve a variety of organic compounds, and has a suitable boiling point, which is convenient for separation and recovery, and is conducive to the progress of the reaction and the purification of the product.
halobenzyl, that is, benzyl halide, in which benzyl (benzyl) is connected to a halogen atom. Methyl is the simplest alkyl group, composed of only one carbon atom and three hydrogen atoms. The difference between halobenzyl and methyl is significant. Halobenzyl is more active in chemical properties due to the presence of halogen atoms, and can undergo various substitution reactions. Methyl is relatively stable and is often used as a component of organic compounds, which affects the physical and chemical properties of compounds.
Main use of (di) methyl tert-butyl ether
Methyl tert-butyl ether is an important chemical raw material and additive. Its primary use is as a gasoline additive. Adding methyl tert-butyl ether to gasoline can effectively improve the octane number of gasoline, enhance the anti-explosion performance of gasoline, make the engine burn more smoothly, reduce the occurrence of knock, and then improve the power performance and fuel economy of automobiles. At the same time, it can also reduce the emission of carbon monoxide and other pollutants in automobile exhaust, which is beneficial to environmental protection.
Furthermore, methyl tert-butyl ether also has important applications in the field of organic synthesis. Because of its specific chemical structure and reactivity, it can be used as a reaction intermediate to participate in many organic synthesis reactions, and is used in the preparation of various fine chemicals and drugs. In chemical production, it is often used as a solvent because it has good solubility, can dissolve a variety of organic compounds, and has a suitable boiling point, which is convenient for separation and recovery, and is conducive to the progress of the reaction and the purification of the product.
What are the synthesis methods of 1- (chlorophenyl-methyl) -2-methylbenzene?
(1) The preparation of halobenzyl-methyl
The preparation of halobenzyl and methyl is an important way for organic synthesis. In the case of halobenzyl, the benzyl group is also a compound connected to the halogen atom; methyl is the group left after the removal of one hydrogen atom from methane. To make halobenzyl, toluene is often used as the starting material and can be obtained by halogenation. If chlorine or bromine is used, under the action of light or initiator, the hydrogen atom in the benzyl position of toluene can be replaced by a halogen atom to produce halobenzyl. In this process, light or initiator can promote the splitting of halogen molecules into free radicals, and then the radical substitution reaction with toluene occurs.
As for the preparation of methyl, it can be started from methanol Methanol under the action of an appropriate catalyst can generate methyl free radicals through dehydration reaction, and then a series of reactions can be used to obtain methyl-containing compounds. There are also halogenated methane as raw materials, and methyl groups are introduced by reacting with metal-organic reagents.
Synthesis of (di) Methylbenzene
Methylbenzene, also known as toluene, has many synthesis methods. First, it can be synthesized from benzene and monochloromethane under the catalysis of anhydrous aluminum trichloride and other Lewis acids by Fu-g alkylation reaction. In this reaction, monochloromethane generates carbon cations under the action of Lewis acid, which attack the benzene ring as an electrophilic reagent, and an electrophilic substitution reaction occurs to generate toluene. However, the reaction requires attention to control the reaction conditions, because the generated toluene is more prone to electrophilic substitution than benzene, and multiple substitution products may be produced.
Second, it can be prepared by the reaction of benzene and methanol under the action of a specific molecular sieve catalyst. This reaction condition is relatively mild, and the molecular sieve catalyst has good form selection, which can reduce the formation of multiple substitution products. During the reaction process, methanol undergoes dehydration and activation on the surface of the catalyst, forming active intermediates to attack the benzene ring and realize the synthesis of methyl benzene.
Third, coal tar is used as raw material, and the aromatic hydrocarbon mixture such as benzene can be obtained by fractionation, and then toluene can be obtained by further separation and refining. Coal tar is a by-product of coal dry distillation, which is rich in a variety of aromatic compounds. After proper treatment, methyl benzene can be effectively obtained.
The preparation of halobenzyl and methyl is an important way for organic synthesis. In the case of halobenzyl, the benzyl group is also a compound connected to the halogen atom; methyl is the group left after the removal of one hydrogen atom from methane. To make halobenzyl, toluene is often used as the starting material and can be obtained by halogenation. If chlorine or bromine is used, under the action of light or initiator, the hydrogen atom in the benzyl position of toluene can be replaced by a halogen atom to produce halobenzyl. In this process, light or initiator can promote the splitting of halogen molecules into free radicals, and then the radical substitution reaction with toluene occurs.
As for the preparation of methyl, it can be started from methanol Methanol under the action of an appropriate catalyst can generate methyl free radicals through dehydration reaction, and then a series of reactions can be used to obtain methyl-containing compounds. There are also halogenated methane as raw materials, and methyl groups are introduced by reacting with metal-organic reagents.
Synthesis of (di) Methylbenzene
Methylbenzene, also known as toluene, has many synthesis methods. First, it can be synthesized from benzene and monochloromethane under the catalysis of anhydrous aluminum trichloride and other Lewis acids by Fu-g alkylation reaction. In this reaction, monochloromethane generates carbon cations under the action of Lewis acid, which attack the benzene ring as an electrophilic reagent, and an electrophilic substitution reaction occurs to generate toluene. However, the reaction requires attention to control the reaction conditions, because the generated toluene is more prone to electrophilic substitution than benzene, and multiple substitution products may be produced.
Second, it can be prepared by the reaction of benzene and methanol under the action of a specific molecular sieve catalyst. This reaction condition is relatively mild, and the molecular sieve catalyst has good form selection, which can reduce the formation of multiple substitution products. During the reaction process, methanol undergoes dehydration and activation on the surface of the catalyst, forming active intermediates to attack the benzene ring and realize the synthesis of methyl benzene.
Third, coal tar is used as raw material, and the aromatic hydrocarbon mixture such as benzene can be obtained by fractionation, and then toluene can be obtained by further separation and refining. Coal tar is a by-product of coal dry distillation, which is rich in a variety of aromatic compounds. After proper treatment, methyl benzene can be effectively obtained.
What are the precautions for 1- (chlorophenyl-methyl) -2-methylbenzene during storage and transportation?
Nowadays, there are silicon groups and methyl groups, silicon groups, which are mainly composed of silicon atoms and are widely used in many fields. Methyl groups are formed by the combination of one carbon atom and three hydrogen atoms. Compared with methyl groups, silicon groups have their own characteristics.
As for methyl silicon, there are indeed many things to pay attention to during storage and transportation. First, you need to be careful to prevent moisture. Methyl silicon is active and easy to react or deteriorate in case of water vapor, so it should be stored in a dry place and packaged tightly to prevent moisture from invading.
Second, temperature is also critical. It should be controlled in a suitable temperature range. If the temperature is too high, it may not promote its chemical reaction and cause performance changes. If the temperature is too low, it may solidify, affecting its flow and service performance. Generally speaking, it should be stored in a cool and well-ventilated place, away from direct sunlight, to avoid large temperature fluctuations.
Third, methyl silicon is flammable. When transporting and storing, it is necessary to keep away from fire and heat sources. Fireworks should be strictly prohibited in the workplace, and fire protection facilities should be complete to prevent accidents.
Fourth, because it may be toxic and irritating, it is necessary to take good protection when operating. Operators wear protective clothing, goggles and gloves in front of them. If they come into contact accidentally, they should rinse with plenty of water immediately and seek medical attention if necessary.
In short, throughout the storage and transportation of methyl silicon, it is necessary to strictly abide by relevant norms and standards, operate with caution, and provide comprehensive protection, so that its performance can be put to good use.
As for methyl silicon, there are indeed many things to pay attention to during storage and transportation. First, you need to be careful to prevent moisture. Methyl silicon is active and easy to react or deteriorate in case of water vapor, so it should be stored in a dry place and packaged tightly to prevent moisture from invading.
Second, temperature is also critical. It should be controlled in a suitable temperature range. If the temperature is too high, it may not promote its chemical reaction and cause performance changes. If the temperature is too low, it may solidify, affecting its flow and service performance. Generally speaking, it should be stored in a cool and well-ventilated place, away from direct sunlight, to avoid large temperature fluctuations.
Third, methyl silicon is flammable. When transporting and storing, it is necessary to keep away from fire and heat sources. Fireworks should be strictly prohibited in the workplace, and fire protection facilities should be complete to prevent accidents.
Fourth, because it may be toxic and irritating, it is necessary to take good protection when operating. Operators wear protective clothing, goggles and gloves in front of them. If they come into contact accidentally, they should rinse with plenty of water immediately and seek medical attention if necessary.
In short, throughout the storage and transportation of methyl silicon, it is necessary to strictly abide by relevant norms and standards, operate with caution, and provide comprehensive protection, so that its performance can be put to good use.
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