Linshang Chemical
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Benzene, 2,6-Dichloro-1-(Chloromethyl)
Linshang Chemical
|
HS Code |
524556 |
| Chemical Formula | C7H5Cl3 |
| Molecular Weight | 195.47 |
| Appearance | Typically a solid (physical state can vary based on conditions) |
| Boiling Point | Data may vary, generally higher due to halogen substitution |
| Melting Point | Specific value depends on purity and measurement method |
| Solubility In Water | Low solubility, as it is an organic compound with non - polar groups |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone |
| Density | Requires experimental determination for precise value |
| Vapor Pressure | Relatively low, due to its non - volatile nature |
| Flash Point | Needs experimental testing to accurately determine |
| Odor | May have a characteristic chloro - aromatic odor |
As an accredited Benzene, 2,6-Dichloro-1-(Chloromethyl) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of 2,6 - dichloro - 1 - (chloromethyl)benzene in a sealed, chemical - resistant bottle. |
| Storage | **Storage of 2,6 - Dichloro - 1 - (chloromethyl)benzene** Store 2,6 - dichloro - 1 - (chloromethyl)benzene in a cool, well - ventilated area, away from heat and ignition sources. Keep it in a tightly closed container made of corrosion - resistant materials, as it may be reactive. Separate from oxidizing agents, bases, and moisture - sensitive substances to prevent chemical reactions. |
| Shipping | "2,6 - Dichloro - 1 - (chloromethyl)benzene is a chemical. Shipping must comply with strict regulations due to its potentially hazardous nature. It should be properly packaged, labeled, and transported by approved carriers." |
Competitive Benzene, 2,6-Dichloro-1-(Chloromethyl) prices that fit your budget—flexible terms and customized quotes for every order.
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What is the main use of this product 2,6-dichloro-1- (chloromethyl) benzene?
This is 2,6-dichloro-1- (chloromethyl) naphthalene, which has a wide range of uses. In the field of medicine, it can act as a key pharmaceutical intermediate to help synthesize drugs with specific therapeutic effects. The special structure contained in this compound can participate in the construction of many drug molecules, giving drugs unique pharmacological activities.
In the field of materials science, it can be used to prepare functional materials with excellent performance. Due to its structural properties, it can play a unique role in the synthesis of materials, giving materials special properties such as excellent optical and electrical properties, so as to meet the special needs of different fields.
In the field of organic synthesis, it is an extremely important starting material and intermediate. With the activity check point in its molecular structure, structural modification and derivatization can be achieved through various organic reactions, and then organic compounds with more complex structures and functions can be synthesized, which promotes the continuous development and innovation of organic synthetic chemistry.
2,6-dichloro-1- (chloromethyl) naphthalene plays an indispensable role in many important fields and is of great significance to the progress and development of related industries.
In the field of materials science, it can be used to prepare functional materials with excellent performance. Due to its structural properties, it can play a unique role in the synthesis of materials, giving materials special properties such as excellent optical and electrical properties, so as to meet the special needs of different fields.
In the field of organic synthesis, it is an extremely important starting material and intermediate. With the activity check point in its molecular structure, structural modification and derivatization can be achieved through various organic reactions, and then organic compounds with more complex structures and functions can be synthesized, which promotes the continuous development and innovation of organic synthetic chemistry.
2,6-dichloro-1- (chloromethyl) naphthalene plays an indispensable role in many important fields and is of great significance to the progress and development of related industries.
What are the physical properties of 2,6-dichloro-1- (chloromethyl) benzene?
2% 2C6-dioxy-1- (oxomethyl) naphthalene is a kind of organic compound. Its physical properties are particularly important, and it is related to many uses and characteristics of this substance.
Looking at its appearance, it is often white to light yellow crystalline, and this color state can be an important characteristic when it is initially identified. Its melting point is within a specific range. This value is stable and identifiable, because the melting point is a key physical constant when identifying organic compounds. By accurately measuring the melting point, the purity of this substance can be determined. If impurities are mixed in, the melting point often changes, or drops or the melting range becomes wider.
Furthermore, the boiling point of this substance is also an important physical property. The boiling point reflects the temperature at which it changes from liquid to gaseous state under a specific pressure. This property has a great impact on the separation and purification of this substance, or in the chemical process involving this substance. Knowing the boiling point, it is possible to design suitable operations such as distillation to achieve the purpose of purification or obtaining this substance.
The solubility of this substance is also worthy of attention. In organic solvents, such as some common aromatic hydrocarbon solvents, it may have a certain solubility, but in water, the solubility is usually very small. This difference in solubility is of great significance in terms of extraction, reaction medium selection, etc. For example, in a chemical reaction, selecting a suitable solvent requires consideration of the solubility of this substance to ensure the smooth progress of the reaction, so that the reactants are fully contacted, and the reaction efficiency is improved.
Its density is also a physical property. Although the value is normal, it is indispensable in the mixing system involving this substance, or in the design of container volume during storage and transportation. Knowing the density can accurately calculate the relationship between the mass and volume of this substance under specific conditions, ensuring that the relevant operation is safe and efficient.
In addition, the volatility of this substance is relatively low, and it is not easy to quickly evaporate into the air under normal temperature and pressure. This characteristic reduces the loss and safety risk caused by volatilization during storage and use. However, it should also be noted that if the ambient temperature rises or under specific pressure conditions, its volatility may change.
Looking at its appearance, it is often white to light yellow crystalline, and this color state can be an important characteristic when it is initially identified. Its melting point is within a specific range. This value is stable and identifiable, because the melting point is a key physical constant when identifying organic compounds. By accurately measuring the melting point, the purity of this substance can be determined. If impurities are mixed in, the melting point often changes, or drops or the melting range becomes wider.
Furthermore, the boiling point of this substance is also an important physical property. The boiling point reflects the temperature at which it changes from liquid to gaseous state under a specific pressure. This property has a great impact on the separation and purification of this substance, or in the chemical process involving this substance. Knowing the boiling point, it is possible to design suitable operations such as distillation to achieve the purpose of purification or obtaining this substance.
The solubility of this substance is also worthy of attention. In organic solvents, such as some common aromatic hydrocarbon solvents, it may have a certain solubility, but in water, the solubility is usually very small. This difference in solubility is of great significance in terms of extraction, reaction medium selection, etc. For example, in a chemical reaction, selecting a suitable solvent requires consideration of the solubility of this substance to ensure the smooth progress of the reaction, so that the reactants are fully contacted, and the reaction efficiency is improved.
Its density is also a physical property. Although the value is normal, it is indispensable in the mixing system involving this substance, or in the design of container volume during storage and transportation. Knowing the density can accurately calculate the relationship between the mass and volume of this substance under specific conditions, ensuring that the relevant operation is safe and efficient.
In addition, the volatility of this substance is relatively low, and it is not easy to quickly evaporate into the air under normal temperature and pressure. This characteristic reduces the loss and safety risk caused by volatilization during storage and use. However, it should also be noted that if the ambient temperature rises or under specific pressure conditions, its volatility may change.
What are the chemical properties of 2,6-dichloro-1- (chloromethyl) benzene?
2% 2C6-dioxy-1- (oxomethyl) naphthalene is one of the organic compounds. Its chemical properties are quite characteristic, and I will describe them in detail today.
First of all, its physical properties, this compound may be a solid under normal conditions, with a specific melting point and boiling point. The melting point is the temperature at which the substance changes from solid to liquid; the boiling point is the temperature at which the liquid state changes to gaseous state. However, the exact value needs to be determined accurately by experiments. Its appearance may be white to light yellow crystalline, which is also a preliminary observation feature.
Furthermore, on its chemical activity. In this molecular structure, the combination of dioxygen, naphthalene ring and oxomethyl gives it unique reactivity. The naphthalene ring is an aromatic structure with high stability, but it can also participate in many electrophilic substitution reactions. The electrophilic substitution is the reaction in which the electrophilic reagent attacks the electron-rich naphthalene ring, causing the hydrogen atom on the ring to be replaced.
The dioxy part can affect the electron cloud distribution of the molecule, or change the electron cloud density at a specific position of the naphthalene ring, which in turn affects the check point selectivity of the electrophilic substitution reaction. The presence of oxygen methyl groups may exhibit unique chemical behaviors in some reactions. The lone pair electrons on its oxygen atoms can participate in coordination and form complexes with metal ions, etc. This property may have potential applications in catalytic reactions and other fields.
At the same time, this compound may undergo redox reactions. Under appropriate oxidation conditions, the naphthalene ring or the dioxy part can be oxidized, resulting in changes in structure and properties; in the case of strong reducing agents, reduction reactions may also occur, such as partial hydrogenation of naphthalene rings to form hydrogenated naphthalene derivatives.
And because it contains oxygen atoms, or can participate in the formation of hydrogen bonds. Interact with molecules containing hydrogen donors to form hydrogen bond networks, which have significant effects on their aggregation behavior and solubility in solution.
In summary, the chemical properties of 2% 2C6 -dioxy-1- (oxomethyl) naphthalene are rich and diverse, and may have important research and application value in many fields such as organic synthesis and materials science.
First of all, its physical properties, this compound may be a solid under normal conditions, with a specific melting point and boiling point. The melting point is the temperature at which the substance changes from solid to liquid; the boiling point is the temperature at which the liquid state changes to gaseous state. However, the exact value needs to be determined accurately by experiments. Its appearance may be white to light yellow crystalline, which is also a preliminary observation feature.
Furthermore, on its chemical activity. In this molecular structure, the combination of dioxygen, naphthalene ring and oxomethyl gives it unique reactivity. The naphthalene ring is an aromatic structure with high stability, but it can also participate in many electrophilic substitution reactions. The electrophilic substitution is the reaction in which the electrophilic reagent attacks the electron-rich naphthalene ring, causing the hydrogen atom on the ring to be replaced.
The dioxy part can affect the electron cloud distribution of the molecule, or change the electron cloud density at a specific position of the naphthalene ring, which in turn affects the check point selectivity of the electrophilic substitution reaction. The presence of oxygen methyl groups may exhibit unique chemical behaviors in some reactions. The lone pair electrons on its oxygen atoms can participate in coordination and form complexes with metal ions, etc. This property may have potential applications in catalytic reactions and other fields.
At the same time, this compound may undergo redox reactions. Under appropriate oxidation conditions, the naphthalene ring or the dioxy part can be oxidized, resulting in changes in structure and properties; in the case of strong reducing agents, reduction reactions may also occur, such as partial hydrogenation of naphthalene rings to form hydrogenated naphthalene derivatives.
And because it contains oxygen atoms, or can participate in the formation of hydrogen bonds. Interact with molecules containing hydrogen donors to form hydrogen bond networks, which have significant effects on their aggregation behavior and solubility in solution.
In summary, the chemical properties of 2% 2C6 -dioxy-1- (oxomethyl) naphthalene are rich and diverse, and may have important research and application value in many fields such as organic synthesis and materials science.
What is the production method of 2,6-dichloro-1- (chloromethyl) benzene?
To make 2-methyl-1- (methoxy) -2-hexene, you can follow the following ancient method.
First take an appropriate amount of hexanal and place it in a clean kettle. Prepare a container, mix methanol with an appropriate amount of strong alkali such as sodium hydroxide, stir well, so that the alkali is fully dissolved to make a methoxylating reagent. Slowly drop this reagent into the kettle containing hexanal, and slowly heat it over a low heat to maintain the temperature in the kettle at a moderate degree, about 40 to 50 degrees Celsius. In this process, the aldehyde group undergoes a nucleophilic addition reaction with the methoxylating reagent. The carbonyl carbon of the aldehyde is attacked by the negative methoxy ion to form a negatively charged intermediate, which is then protonated to obtain an alcohol containing methoxy group.
The obtained product is moved to another device, and an appropriate amount of concentrated sulfuric acid is added as a dehydrating agent. Heating is heated to 120 to 130 degrees Celsius to promote an intramolecular dehydration reaction of the alcohol. The hydroxyl group is combined with the hydrogen atom on the adjacent carbon to form a water dehydration, and at the same time, a carbon-carbon double bond is formed, resulting in a crude product of 2-methyl-1- (methoxy) -2-hexene.
However, the crude product may contain impurities and needs to be purified by distillation. The crude product is placed in a still, and the distillation temperature and pressure are controlled according to the boiling point characteristics of the target product. Collect the fractions within a specific temperature range, which is pure 2-methyl-1- (methoxy) -2-hexene. During the operation, be sure to pay attention to the control of heat, reagent dosage and reaction time to ensure a smooth reaction and good product yield and purity.
First take an appropriate amount of hexanal and place it in a clean kettle. Prepare a container, mix methanol with an appropriate amount of strong alkali such as sodium hydroxide, stir well, so that the alkali is fully dissolved to make a methoxylating reagent. Slowly drop this reagent into the kettle containing hexanal, and slowly heat it over a low heat to maintain the temperature in the kettle at a moderate degree, about 40 to 50 degrees Celsius. In this process, the aldehyde group undergoes a nucleophilic addition reaction with the methoxylating reagent. The carbonyl carbon of the aldehyde is attacked by the negative methoxy ion to form a negatively charged intermediate, which is then protonated to obtain an alcohol containing methoxy group.
The obtained product is moved to another device, and an appropriate amount of concentrated sulfuric acid is added as a dehydrating agent. Heating is heated to 120 to 130 degrees Celsius to promote an intramolecular dehydration reaction of the alcohol. The hydroxyl group is combined with the hydrogen atom on the adjacent carbon to form a water dehydration, and at the same time, a carbon-carbon double bond is formed, resulting in a crude product of 2-methyl-1- (methoxy) -2-hexene.
However, the crude product may contain impurities and needs to be purified by distillation. The crude product is placed in a still, and the distillation temperature and pressure are controlled according to the boiling point characteristics of the target product. Collect the fractions within a specific temperature range, which is pure 2-methyl-1- (methoxy) -2-hexene. During the operation, be sure to pay attention to the control of heat, reagent dosage and reaction time to ensure a smooth reaction and good product yield and purity.
What are the precautions for using 2,6-dichloro-1- (chloromethyl) benzene?
2% 2C6-dioxy-1- (oxomethyl) benzene. Many precautions should be kept in mind during use.
First safety protection. This substance is dangerous, and appropriate protective equipment must be worn when operating. If you wear high-quality protective gloves, it can block skin contact with it and prevent skin irritation or absorption damage; wear tight goggles to protect your eyes and avoid eye damage caused by splashing; wear protective clothing to protect the body in all directions and reduce the risk of exposure.
Furthermore, the operating environment is crucial. Work in a well-ventilated place, preferably in a fume hood. Good ventilation can disperse volatile gas in time, reduce the concentration in the air, and avoid health damage caused by inhalation. If used in a poorly ventilated place, gas accumulation, or poisoning and other serious consequences.
Storage is also exquisite. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its flammability, in case of open flames and hot topics, it may cause combustion or even explosion. And it should be stored separately from oxidants, acids, etc., to prevent dangerous chemical reactions.
When taking it, strictly follow the specifications. Measure it with a precise measuring tool to avoid waste and excess. After operation, properly dispose of the residue and waste, do not discard it at will, and dispose of it centrally in accordance with relevant regulations to prevent environmental pollution.
Use 2% 2C6 -dioxy-1- (oxomethyl) benzene with care in all aspects to ensure personal safety, environmental safety and operating standards.
First safety protection. This substance is dangerous, and appropriate protective equipment must be worn when operating. If you wear high-quality protective gloves, it can block skin contact with it and prevent skin irritation or absorption damage; wear tight goggles to protect your eyes and avoid eye damage caused by splashing; wear protective clothing to protect the body in all directions and reduce the risk of exposure.
Furthermore, the operating environment is crucial. Work in a well-ventilated place, preferably in a fume hood. Good ventilation can disperse volatile gas in time, reduce the concentration in the air, and avoid health damage caused by inhalation. If used in a poorly ventilated place, gas accumulation, or poisoning and other serious consequences.
Storage is also exquisite. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because of its flammability, in case of open flames and hot topics, it may cause combustion or even explosion. And it should be stored separately from oxidants, acids, etc., to prevent dangerous chemical reactions.
When taking it, strictly follow the specifications. Measure it with a precise measuring tool to avoid waste and excess. After operation, properly dispose of the residue and waste, do not discard it at will, and dispose of it centrally in accordance with relevant regulations to prevent environmental pollution.
Use 2% 2C6 -dioxy-1- (oxomethyl) benzene with care in all aspects to ensure personal safety, environmental safety and operating standards.
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