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1-[Bromo(Phenyl)Methyl]-4-Chlorobenzene
Linshang Chemical
|
HS Code |
486883 |
| Chemical Formula | C13H10BrCl |
| Molar Mass | 281.58 g/mol |
| Appearance | Solid (predicted) |
| Solubility In Water | Low (organic compound, likely hydrophobic) |
| Solubility In Organic Solvents | Soluble in common organic solvents like dichloromethane, chloroform |
| Logp | Positive (hydrophobic, likely to partition into non - polar phases) |
| Vapor Pressure | Low (solid, relatively non - volatile) |
As an accredited 1-[Bromo(Phenyl)Methyl]-4-Chlorobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 100g of 1 - [bromo(phenyl)methyl]-4 - chlorobenzene in sealed, labeled chemical container. |
| Storage | 1 - [Bromo(phenyl)methyl]-4 - chlorobenzene 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 leakage and exposure to air and moisture, which could potentially cause decomposition or reactivity issues. |
| Shipping | 1 - [bromo(phenyl)methyl]-4 - chlorobenzene is shipped in sealed, corrosion - resistant containers. Special handling procedures are followed to prevent spills, with proper labeling indicating its chemical nature and safety precautions. |
Competitive 1-[Bromo(Phenyl)Methyl]-4-Chlorobenzene prices that fit your budget—flexible terms and customized quotes for every order.
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Where to Buy 1-[Bromo(Phenyl)Methyl]-4-Chlorobenzene in China?
As a trusted 1-[Bromo(Phenyl)Methyl]-4-Chlorobenzene manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery.
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-[Bromo(Phenyl)Methyl]-4-Chlorobenzene supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
What are the main uses of 1- [ (bromo (phenyl)) methyl] -4-chlorobenzene?
(Boron (silicon-based)) methyl, this chemical substance and 4-chlorosilane, have important uses in the chemical industry.
Borosilicate methyl compounds are widely used in the field of materials science. In the preparation of advanced ceramic materials, borosilicate methyl can be used as a precursor. Due to its structural properties, it can promote the formation of specific microstructures in ceramic materials through complex chemical reactions under high temperatures and other conditions, improving the mechanical properties and chemical stability of materials. For example, high-temperature ceramic parts used in the aerospace field, borosilicate methyl is involved in the preparation of materials that can withstand extreme temperatures and mechanical stresses, ensuring stable operation of components in harsh environments.
4-chlorosilane plays a key role in organic synthesis chemistry. It is often used as a silicon source reagent and participates in the synthesis of many silicone compounds. Due to its high chlorine atom activity, it is easy to replace with a variety of organic functional groups, and then build a variety of silicone structures. For example, 4-chlorosilane is an indispensable starting material when preparing silicone polymers such as high-performance silicone oil and silicone rubber. Through careful design of reaction paths and conditions, the molecular structure and properties of polymers can be precisely regulated to meet the special needs of different industrial fields for silicone materials. For example, high-insulating and high-flexibility silicone materials used in the electronics industry rely on 4-chlorosilane for synthesis. Boron (silyl) methyl and 4-chlorosilane provide important support for the research and development of new materials and the preparation of high-performance compounds by virtue of their unique chemical properties and reactivity in many branches of chemical industry, and promote the chemical industry to continuously move towards a higher technical level.
Borosilicate methyl compounds are widely used in the field of materials science. In the preparation of advanced ceramic materials, borosilicate methyl can be used as a precursor. Due to its structural properties, it can promote the formation of specific microstructures in ceramic materials through complex chemical reactions under high temperatures and other conditions, improving the mechanical properties and chemical stability of materials. For example, high-temperature ceramic parts used in the aerospace field, borosilicate methyl is involved in the preparation of materials that can withstand extreme temperatures and mechanical stresses, ensuring stable operation of components in harsh environments.
4-chlorosilane plays a key role in organic synthesis chemistry. It is often used as a silicon source reagent and participates in the synthesis of many silicone compounds. Due to its high chlorine atom activity, it is easy to replace with a variety of organic functional groups, and then build a variety of silicone structures. For example, 4-chlorosilane is an indispensable starting material when preparing silicone polymers such as high-performance silicone oil and silicone rubber. Through careful design of reaction paths and conditions, the molecular structure and properties of polymers can be precisely regulated to meet the special needs of different industrial fields for silicone materials. For example, high-insulating and high-flexibility silicone materials used in the electronics industry rely on 4-chlorosilane for synthesis. Boron (silyl) methyl and 4-chlorosilane provide important support for the research and development of new materials and the preparation of high-performance compounds by virtue of their unique chemical properties and reactivity in many branches of chemical industry, and promote the chemical industry to continuously move towards a higher technical level.
What are the physical properties of 1- [ (bromo (phenyl)) methyl] -4-chlorobenzene
"Tiangong Kaiwu" cloud: Mercury (that is, mercury), its quality is clear, its color is silver-white, and it is a liquid at room temperature. It flows amorphously, like a melt of silver, with a metallic luster.
Mercury has specific properties. First, it is volatile. It slowly dissolves gas and disperses in an open place at room temperature. Although it is invisible and colorless, it is latent in toxicity. Second, its solubility is quite different. It can dissolve metals, such as gold, silver, lead, and tin, and combine them to form amalgam. Third, it is chemically active and can quickly combine with sulfur to form mercury sulfide. The color is vermilion, which is the genus of cinnabar.
Ruoyan 1- [ (mercury (silver)) ethyl] -4 -silver chloride, this is an organic mercury compound and the like. Organic mercury substances have complex properties. They have certain chemical activities. Under specific conditions, mercury atoms can react with surrounding atomic groups, break bonds and recombine, or participate in chemical synthesis.
Organic mercury compounds are often toxic due to the presence of mercury in the molecular structure. Mercury atoms can bind to the activity check points of proteins and enzymes in organisms, disrupt physiological and biochemical processes, damage nerves, liver and kidney and other organs. Moreover, such compounds are difficult to decompose in the environment, easy to accumulate, and endanger the ecology.
And organic mercury in different media, its physical properties are also different. Or in organic solvents with a certain solubility, or in the aqueous phase dispersion state is different, depending on its molecular structure, group characteristics.
Mercury has specific properties. First, it is volatile. It slowly dissolves gas and disperses in an open place at room temperature. Although it is invisible and colorless, it is latent in toxicity. Second, its solubility is quite different. It can dissolve metals, such as gold, silver, lead, and tin, and combine them to form amalgam. Third, it is chemically active and can quickly combine with sulfur to form mercury sulfide. The color is vermilion, which is the genus of cinnabar.
Ruoyan 1- [ (mercury (silver)) ethyl] -4 -silver chloride, this is an organic mercury compound and the like. Organic mercury substances have complex properties. They have certain chemical activities. Under specific conditions, mercury atoms can react with surrounding atomic groups, break bonds and recombine, or participate in chemical synthesis.
Organic mercury compounds are often toxic due to the presence of mercury in the molecular structure. Mercury atoms can bind to the activity check points of proteins and enzymes in organisms, disrupt physiological and biochemical processes, damage nerves, liver and kidney and other organs. Moreover, such compounds are difficult to decompose in the environment, easy to accumulate, and endanger the ecology.
And organic mercury in different media, its physical properties are also different. Or in organic solvents with a certain solubility, or in the aqueous phase dispersion state is different, depending on its molecular structure, group characteristics.
What are the chemical properties of 1- [ (bromo (phenyl)) methyl] -4-chlorobenzene
In Taoist alchemy, the chemicals involved in "1 - [ (immersed (mercury-based)) ethyl] -4 -mercury chloride" have many specific chemical properties.
Mercury is a liquid metal at room temperature, with a silver luster and strong volatility. In "1 - [ (immersed (mercury-based)) ethyl] -4 -mercury chloride", mercury is a key element, which is connected with other groups to build a unique chemical structure. Its chemical activity is affected by the presence of surrounding groups. The introduction of ethyl may change the lipophilicity of the substance, and its solubility in organic solvents may vary. The participation of chlorine atoms results in changes in molecular polarity due to the strong electronegativity of chlorine, which affects its interaction with other substances.
Furthermore, the stability of this chemical substance is also an important property. The strength of the chemical bond between mercury and ethyl and chlorine atoms determines whether it can exist stably under different environmental conditions. In the event of heat, light or specific chemical reaction conditions, or the chemical bond is broken, causing the substance to decompose or undergo chemical transformation.
In addition, the redox properties of this substance are also worthy of attention. Under appropriate conditions, the variable valence state of mercury may undergo a redox reaction, changing its own valence state and promoting the oxidation or reduction of other substances. These redox processes, or lead to a series of chain chemical reactions, in the process of alchemy, or have a profound impact on the formation and properties of medicinal pills.
However, it needs to be understood that although ancient alchemy contained simple chemical exploration, it was limited to the level of cognition and technology at that time, and the understanding of many chemical substances was still shallow. Today, from a scientific perspective, the research of such substances needs to strictly follow modern chemical theory and experimental norms in order to gain a deep understanding of their chemical properties and potential applications.
Mercury is a liquid metal at room temperature, with a silver luster and strong volatility. In "1 - [ (immersed (mercury-based)) ethyl] -4 -mercury chloride", mercury is a key element, which is connected with other groups to build a unique chemical structure. Its chemical activity is affected by the presence of surrounding groups. The introduction of ethyl may change the lipophilicity of the substance, and its solubility in organic solvents may vary. The participation of chlorine atoms results in changes in molecular polarity due to the strong electronegativity of chlorine, which affects its interaction with other substances.
Furthermore, the stability of this chemical substance is also an important property. The strength of the chemical bond between mercury and ethyl and chlorine atoms determines whether it can exist stably under different environmental conditions. In the event of heat, light or specific chemical reaction conditions, or the chemical bond is broken, causing the substance to decompose or undergo chemical transformation.
In addition, the redox properties of this substance are also worthy of attention. Under appropriate conditions, the variable valence state of mercury may undergo a redox reaction, changing its own valence state and promoting the oxidation or reduction of other substances. These redox processes, or lead to a series of chain chemical reactions, in the process of alchemy, or have a profound impact on the formation and properties of medicinal pills.
However, it needs to be understood that although ancient alchemy contained simple chemical exploration, it was limited to the level of cognition and technology at that time, and the understanding of many chemical substances was still shallow. Today, from a scientific perspective, the research of such substances needs to strictly follow modern chemical theory and experimental norms in order to gain a deep understanding of their chemical properties and potential applications.
What is the synthesis method of 1- [ (bromo (phenyl)) methyl] -4-chlorobenzene
To prepare 1- [ (cyanogen (benzyl)) methyl] -4-bromobenzyl, the following ancient method can be used.
Take benzyl cyanide first and treat it with a strong base such as sodium hydride ($NaH $). Sodium hydride in inert solvents such as tetrahydrofuran ($THF $) can capture benzyl cyanide alpha-hydrogen to generate carbon anion. This step is due to the electron-absorbing properties of the cyano group, making alpha-hydrogen acidic to a certain extent. React with strong bases:
$C_6H_5CH_2CN + NaH\ xrightarrow [] {THF} C_6H_5\ overline {C} HCN + H_2\ uparrow + Na ^ + $
Then, the generated carboanion is mixed with bromomethane ($CH_3Br $). The negative carbon ions have strong nucleophilicity and can attack the carbon of bromomethane. The bromine ions leave to give 1- [ (cyanogen (benzyl)) methyl]:
$C_6H_5\ overline {C} HCN + CH_3Br\ longrightarrow C_6H_5CH (CN) CH_3 $
and then take 1- [ (cyanogen (benzyl)) methyl]. React with brominating reagents such as bromine ($Br_2 $) in the presence of light or free radical initiators such as benzoyl peroxide ($BPO $). Due to the double influence of benzyl ring and cyanyl group, the hydrogen at the benzyl position is easily replaced by bromine under the condition of free radical reaction to form the target product 1 - [ (cyanide (benzyl)) methyl] - 4 -bromobenzyl:
$C_6H_5CH (CN) CH_3 + Br_2\ xrightarrow [] {light/BPO} C_6H_4BrCH (CN) CH_3 + HBr $
Alternatively, benzyl bromide and sodium cyanide ($NaCN $) can undergo nucleophilic substitution reaction to obtain benzyl cyanide:
$C_6H_5CH_2Br + NaCN\ rightarrow C_6H_5CH_2CN + NaBr $
Finally brominated, the target product can also be obtained. When operating, it is necessary to pay attention to the reaction conditions at each step. The choice of solvent and the dosage of reagents are all related to the success or failure of the reaction, and many reagents are toxic and corrosive. It is necessary to operate with caution and adhere to safety procedures.
Take benzyl cyanide first and treat it with a strong base such as sodium hydride ($NaH $). Sodium hydride in inert solvents such as tetrahydrofuran ($THF $) can capture benzyl cyanide alpha-hydrogen to generate carbon anion. This step is due to the electron-absorbing properties of the cyano group, making alpha-hydrogen acidic to a certain extent. React with strong bases:
$C_6H_5CH_2CN + NaH\ xrightarrow [] {THF} C_6H_5\ overline {C} HCN + H_2\ uparrow + Na ^ + $
Then, the generated carboanion is mixed with bromomethane ($CH_3Br $). The negative carbon ions have strong nucleophilicity and can attack the carbon of bromomethane. The bromine ions leave to give 1- [ (cyanogen (benzyl)) methyl]:
$C_6H_5\ overline {C} HCN + CH_3Br\ longrightarrow C_6H_5CH (CN) CH_3 $
and then take 1- [ (cyanogen (benzyl)) methyl]. React with brominating reagents such as bromine ($Br_2 $) in the presence of light or free radical initiators such as benzoyl peroxide ($BPO $). Due to the double influence of benzyl ring and cyanyl group, the hydrogen at the benzyl position is easily replaced by bromine under the condition of free radical reaction to form the target product 1 - [ (cyanide (benzyl)) methyl] - 4 -bromobenzyl:
$C_6H_5CH (CN) CH_3 + Br_2\ xrightarrow [] {light/BPO} C_6H_4BrCH (CN) CH_3 + HBr $
Alternatively, benzyl bromide and sodium cyanide ($NaCN $) can undergo nucleophilic substitution reaction to obtain benzyl cyanide:
$C_6H_5CH_2Br + NaCN\ rightarrow C_6H_5CH_2CN + NaBr $
Finally brominated, the target product can also be obtained. When operating, it is necessary to pay attention to the reaction conditions at each step. The choice of solvent and the dosage of reagents are all related to the success or failure of the reaction, and many reagents are toxic and corrosive. It is necessary to operate with caution and adhere to safety procedures.
What are the precautions for storing and transporting 1- [ (bromo (phenyl)) methyl] -4-chlorobenzene?
Methylmercury of mercury (based on mercury), as well as methylmercury of mercury (based on mercury), should be kept in mind.
Methylmercury of mercury (based on mercury), which is toxic to humans. It is easy to accumulate in the environment, follow the food, and gather in biological. In the place where it is stored, a special seal container must be used to prevent exposure. Containers should be resistant to corrosion, because mercury and its compounds are corrosive. And in the place where it is stored, it must be dry, dry, and well-connected, and the source of ignition, Because of its chemical activity, in case of specific pieces, or strong reaction. Workers should contact it, and use protective clothing, such as protective clothing, gloves, masks, etc., to prevent skin contact Inhalation.
In the process of storage, it is also not allowed to be small. The reliability is not low, and the sensitivity and force are sensitive. If it is not stored, it should be placed in the environment of the environment and the environment, and the wave should be controlled. On the way, the warehouse needs to be equipped with a fixed setting to prevent strong shocks and collisions. Its packaging is also low, so as to prevent earthquakes and leaks. People must be trained, familiar with the characteristics and emergency treatment methods. In the event of a leakage accident, positive measures can be quickly taken, such as evacuation of crowds, sealing, and adsorption treatment, etc., to reduce harm.
Therefore, mercury (methyl mercury), due to its special risk, must be operated in accordance with regulations for all types of storage, and a high degree of safety is required in order to effectively prevent accidents and ensure human safety.
Methylmercury of mercury (based on mercury), which is toxic to humans. It is easy to accumulate in the environment, follow the food, and gather in biological. In the place where it is stored, a special seal container must be used to prevent exposure. Containers should be resistant to corrosion, because mercury and its compounds are corrosive. And in the place where it is stored, it must be dry, dry, and well-connected, and the source of ignition, Because of its chemical activity, in case of specific pieces, or strong reaction. Workers should contact it, and use protective clothing, such as protective clothing, gloves, masks, etc., to prevent skin contact Inhalation.
In the process of storage, it is also not allowed to be small. The reliability is not low, and the sensitivity and force are sensitive. If it is not stored, it should be placed in the environment of the environment and the environment, and the wave should be controlled. On the way, the warehouse needs to be equipped with a fixed setting to prevent strong shocks and collisions. Its packaging is also low, so as to prevent earthquakes and leaks. People must be trained, familiar with the characteristics and emergency treatment methods. In the event of a leakage accident, positive measures can be quickly taken, such as evacuation of crowds, sealing, and adsorption treatment, etc., to reduce harm.
Therefore, mercury (methyl mercury), due to its special risk, must be operated in accordance with regulations for all types of storage, and a high degree of safety is required in order to effectively prevent accidents and ensure human safety.
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