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3-Chloro-1-Propenyl)Benzene
Linshang Chemical
|
HS Code |
615462 |
| Chemical Formula | C9H9Cl |
| Molar Mass | 152.62 g/mol |
| Appearance | Liquid (usually) |
| Boiling Point | Estimated around 200 - 220 °C (approximate, can vary based on purity and pressure) |
| Density | Approx. 1.05 - 1.1 g/cm³ (estimated) |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether, etc. |
| Odor | Typical aromatic - chlorinated hydrocarbon odor |
| Flash Point | Probably in the range of 70 - 90 °C (estimated) |
As an accredited 3-Chloro-1-Propenyl)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of (3 - chloro - 1 - propenyl)benzene packaged in a sealed, chemical - resistant bottle. |
| Storage | (3 - chloro - 1 - propenyl)benzene should be stored in a cool, well - ventilated area away from direct sunlight. Keep it in a tightly sealed container to prevent evaporation and exposure to air. Store it separately from oxidizing agents and incompatible substances. Ensure the storage location has proper spill - containment measures due to its potential hazards. |
| Shipping | (3 - chloro - 1 - propenyl)benzene is shipped in well - sealed, corrosion - resistant containers. It must comply with hazardous chemical shipping regulations, ensuring proper labeling and safe handling during transportation to prevent spills and environmental risks. |
Competitive 3-Chloro-1-Propenyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
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As a leading 3-Chloro-1-Propenyl)Benzene 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 chemical properties of 3- (chloro-1-propenyl) benzene?
(1-Methylphenyl) silicon, which is a silicon compound. Its chemical properties are characteristic and have important uses in many domains.
In this compound, the silicon atom has a specific group phase. In terms of reactivity, (1-methylphenyl) silicon can exhibit multi-reactive properties. Due to the presence of a group on the silicon atom, its sub-cloud is similar to that of ordinary silicon compounds, so it shows a special activity in the reactive reaction of the silicon nucleus substitution.
In some synthetic reactive compounds, (1-methylphenyl) silicon can be filled with reactive silicon. For example, in some studies aimed at building a silicon skeleton, it can generate reactions such as generation, and through the formation of silicon-carbon, it can achieve the functionalization of molecules.
Furthermore, (-1-methylphenyl) silicon also has a certain degree of quality. In high-resolution environments, it can still maintain its own stability without rapid decomposition or rearrangement. This property makes it useful in some processes that require high-quality processing, such as in the process of some high-quality materials, which can be added to improve the properties of materials.
In addition, its solubility in solution also has its own characteristics. Depending on the solubility of silicon, (1-methylphenyl) silicon can exhibit different degrees of solubility. In non-soluble solutions, it often has good solubility due to the non-soluble properties of methyl, while in soluble solutions, solubility or solubility is limited to a certain extent. As a result, (1-methylphenyl) silicon is rich in chemical properties and has a lot of solubility in chemical synthesis, materials science and other fields.
In this compound, the silicon atom has a specific group phase. In terms of reactivity, (1-methylphenyl) silicon can exhibit multi-reactive properties. Due to the presence of a group on the silicon atom, its sub-cloud is similar to that of ordinary silicon compounds, so it shows a special activity in the reactive reaction of the silicon nucleus substitution.
In some synthetic reactive compounds, (1-methylphenyl) silicon can be filled with reactive silicon. For example, in some studies aimed at building a silicon skeleton, it can generate reactions such as generation, and through the formation of silicon-carbon, it can achieve the functionalization of molecules.
Furthermore, (-1-methylphenyl) silicon also has a certain degree of quality. In high-resolution environments, it can still maintain its own stability without rapid decomposition or rearrangement. This property makes it useful in some processes that require high-quality processing, such as in the process of some high-quality materials, which can be added to improve the properties of materials.
In addition, its solubility in solution also has its own characteristics. Depending on the solubility of silicon, (1-methylphenyl) silicon can exhibit different degrees of solubility. In non-soluble solutions, it often has good solubility due to the non-soluble properties of methyl, while in soluble solutions, solubility or solubility is limited to a certain extent. As a result, (1-methylphenyl) silicon is rich in chemical properties and has a lot of solubility in chemical synthesis, materials science and other fields.
What are the physical properties of 3- (chloro-1-propenyl) benzene?
(-1 -Methylphenoxy) benzene, also known as phenoxy, is a complex compound. Its physical properties are as follows:
On the outer surface, it is often white and solid. Under normal conditions, the properties are determined, and this shape is easy to survive.
In terms of melting, it is between 78 and 80 ° C. At this temperature, the material starts from solid to liquid. This melting property is important in chemical production and phase applications, and it is important to control the phase and improve the refining process.
On the boiling surface, due to factors such as molecular force, it is usually determined under a specific force. However, because it is not boiling, it may decompose due to high temperature, so the fine value of the boiling surface is slightly different in different texts or materials.
In terms of solubility, it has low solubility in water and is soluble in water. However, in many solvents, such as acetone, dichloromethane, and toluene, it can dissolve (1-methylphenoxy) benzene well. This solubility property is very important in the process of its solubility, separation, extraction, and preparation of active ingredients. It can be used to complete various operations according to its solubility. In terms of density,
has a certain density, and the density is slightly different due to the determined value, but it is roughly in a specific range. The density is a physical property, which provides an important test basis in considering its distribution in the mixing system, flow performance, and the calculation of the amount used in some processes.
In terms of performance, the phase performance is low, and the speed is slow under normal conditions. This characteristic makes it possible to maintain a certain content of the phase in a certain range during the storage and use process, reduce the loss caused by it, and improve its effectiveness for other purposes.
On the outer surface, it is often white and solid. Under normal conditions, the properties are determined, and this shape is easy to survive.
In terms of melting, it is between 78 and 80 ° C. At this temperature, the material starts from solid to liquid. This melting property is important in chemical production and phase applications, and it is important to control the phase and improve the refining process.
On the boiling surface, due to factors such as molecular force, it is usually determined under a specific force. However, because it is not boiling, it may decompose due to high temperature, so the fine value of the boiling surface is slightly different in different texts or materials.
In terms of solubility, it has low solubility in water and is soluble in water. However, in many solvents, such as acetone, dichloromethane, and toluene, it can dissolve (1-methylphenoxy) benzene well. This solubility property is very important in the process of its solubility, separation, extraction, and preparation of active ingredients. It can be used to complete various operations according to its solubility. In terms of density,
has a certain density, and the density is slightly different due to the determined value, but it is roughly in a specific range. The density is a physical property, which provides an important test basis in considering its distribution in the mixing system, flow performance, and the calculation of the amount used in some processes.
In terms of performance, the phase performance is low, and the speed is slow under normal conditions. This characteristic makes it possible to maintain a certain content of the phase in a certain range during the storage and use process, reduce the loss caused by it, and improve its effectiveness for other purposes.
What are the main uses of 3- (chloro-1-propenyl) benzene?
(B-1 -methylbenzyl) ether, namely methyl benzyl ether, its main use is wide.
In the field of synthesis, methyl benzyl ether is often used as a protective group. Because benzyl can be introduced into the molecule by a multi-way, and the phase stability can be maintained under the multi-reaction member. To complete the required reaction, the benzyl can be removed from the specific reaction member, so that the functional activity of the protected product can be restored. For example, in the reaction of alcohol compounds, to avoid unnecessary reaction of the alcohol group in some reactions, it can be guaranteed in the form of methylbenzyl ether. In this way, when the reaction is performed in other functions, the alcohol group can be preserved. When the whole reaction is close to the end, the benzyl group can be removed by methods such as catalytic solution, and the original alcohol group can be released.
In addition, methyl benzyl ether also has a place in the fragrance industry. Because of its unique taste, it can be used as a fragrance component, and fragrance products add a special fragrance. It is used in perfumes, air fresheners, toiletries, etc., to give it a pleasant taste.
In addition, in some methods of chemical synthesis, methyl benzyl ether may also exist in the process. Through its step-by-step modification, it can build molecules with specific biological activities, which can help the research and production of new products.
In the field of synthesis, methyl benzyl ether is often used as a protective group. Because benzyl can be introduced into the molecule by a multi-way, and the phase stability can be maintained under the multi-reaction member. To complete the required reaction, the benzyl can be removed from the specific reaction member, so that the functional activity of the protected product can be restored. For example, in the reaction of alcohol compounds, to avoid unnecessary reaction of the alcohol group in some reactions, it can be guaranteed in the form of methylbenzyl ether. In this way, when the reaction is performed in other functions, the alcohol group can be preserved. When the whole reaction is close to the end, the benzyl group can be removed by methods such as catalytic solution, and the original alcohol group can be released.
In addition, methyl benzyl ether also has a place in the fragrance industry. Because of its unique taste, it can be used as a fragrance component, and fragrance products add a special fragrance. It is used in perfumes, air fresheners, toiletries, etc., to give it a pleasant taste.
In addition, in some methods of chemical synthesis, methyl benzyl ether may also exist in the process. Through its step-by-step modification, it can build molecules with specific biological activities, which can help the research and production of new products.
What are the synthesis methods of 3- (chloro-1-propenyl) benzene?
To prepare 3- (alkyl-1-isopropylphenyl) naphthalene, the following methods can be used:
First, the naphthalene is used as the beginning, and it is first alkylated by Friedel-Crafts. The naphthalene is preferentially reacted with isopropylation reagents, such as isopropyl chloride or isopropyl alcohol, under the catalysis of Lewis acid (such as anhydrous aluminum trichloride), and the α position of the naphthalene is preferentially reacted to obtain 1-isopropylnaphthalene. Subsequently, 1-isopropylnaphthalene and halogenated alkanes (such as halogenated n-alkanes) are introduced into the other ring of the naphthalene ring under the catalysis of similar Due to the high activity of the naphthalene ring, multiple substitution by-products may be generated, so the precise regulation of the reaction conditions is crucial.
Second, the Suzuki coupling reaction is used. First, borate esters or boric acids containing naphthalenyl groups are prepared, and halogenated aromatics containing alkyl-1-isopropylphenyl groups are prepared. Borate esters or boric acids can be obtained by metallizing the corresponding halogenated naphthalenes, such as with n-butyl lithium, and then reacting with borate ester reagents. Halogenated aromatics containing alkyl-1-isopropylphenyl groups can be prepared by halogenating isopropylbenzene and introducing alkyl-1-groups. In the presence of palladium catalysts (such as tetrakis (triphenylphosphine) palladium (0)) and bases (such as potassium carbonate), the target product can be obtained by reacting in a suitable solvent (such as a mixed solvent of dioxane and water). This method has good regioselectivity and can effectively avoid unnecessary side reactions, so the preparation steps of raw materials are slightly complicated.
Third, through the Diels-Alder reaction strategy. Design suitable dienes and dienes. Conjugated dienes with appropriate substituents and alkyl-1-isopropylphenyl derivatives containing ethylenes are used as raw materials. Dienes can be synthesized in multiple steps to ensure their reactivity and selectivity. The preparation of dienophiles also requires multi-step reactions to precisely control the position and structure of the substituents. Under heating or lighting conditions, the Diels-Alder reaction occurs to construct the naphthalene ring structure, and then the subsequent functional group conversion can obtain 3- (alkane-1-isopropylphenyl) naphthalene. This method can construct complex carbon ring structures in one step, but requires strict raw material design and reaction conditions.
First, the naphthalene is used as the beginning, and it is first alkylated by Friedel-Crafts. The naphthalene is preferentially reacted with isopropylation reagents, such as isopropyl chloride or isopropyl alcohol, under the catalysis of Lewis acid (such as anhydrous aluminum trichloride), and the α position of the naphthalene is preferentially reacted to obtain 1-isopropylnaphthalene. Subsequently, 1-isopropylnaphthalene and halogenated alkanes (such as halogenated n-alkanes) are introduced into the other ring of the naphthalene ring under the catalysis of similar Due to the high activity of the naphthalene ring, multiple substitution by-products may be generated, so the precise regulation of the reaction conditions is crucial.
Second, the Suzuki coupling reaction is used. First, borate esters or boric acids containing naphthalenyl groups are prepared, and halogenated aromatics containing alkyl-1-isopropylphenyl groups are prepared. Borate esters or boric acids can be obtained by metallizing the corresponding halogenated naphthalenes, such as with n-butyl lithium, and then reacting with borate ester reagents. Halogenated aromatics containing alkyl-1-isopropylphenyl groups can be prepared by halogenating isopropylbenzene and introducing alkyl-1-groups. In the presence of palladium catalysts (such as tetrakis (triphenylphosphine) palladium (0)) and bases (such as potassium carbonate), the target product can be obtained by reacting in a suitable solvent (such as a mixed solvent of dioxane and water). This method has good regioselectivity and can effectively avoid unnecessary side reactions, so the preparation steps of raw materials are slightly complicated.
Third, through the Diels-Alder reaction strategy. Design suitable dienes and dienes. Conjugated dienes with appropriate substituents and alkyl-1-isopropylphenyl derivatives containing ethylenes are used as raw materials. Dienes can be synthesized in multiple steps to ensure their reactivity and selectivity. The preparation of dienophiles also requires multi-step reactions to precisely control the position and structure of the substituents. Under heating or lighting conditions, the Diels-Alder reaction occurs to construct the naphthalene ring structure, and then the subsequent functional group conversion can obtain 3- (alkane-1-isopropylphenyl) naphthalene. This method can construct complex carbon ring structures in one step, but requires strict raw material design and reaction conditions.
What are the precautions for storing and transporting 3- (chloro-1-propenyl) benzene?
3- (1-methylphenyl) naphthalene should be stored in the environment. Please pay attention to the following general things:
First, this substance may have specific chemical activity, so it needs to be cleared, dry and good. Do not put oxidized, acid, and other substances in the same room, so as not to breed strong chemical reactions and endanger safety. Due to its nature, if exposed to moisture, it is feared that the reaction such as hydrolysis will cause the product to suffer.
There are also many conditions that need to be observed. The container must be tightly sealed to prevent leakage. In this way, it is necessary to fully consider the dangerous characteristics of this object. If it is flammable, it should be equipped with fire equipment, and the road should be avoided in densely populated and important places.
In addition, if it does not exist or does not exist, it should be well-known to all people. Familiar with the characteristics, hazards and emergency measures of this object. In the event of an accident such as leakage, it can quickly follow the established emergency case and take proper measures, such as isolation, evacuation, collection of leakage, etc., to minimize the harm.
Therefore, the storage of 3- (1-methylphenyl) naphthalene requires comprehensive consideration of the environment, containers, people, etc., and the relevant operating procedures are followed in order to ensure the safety of the entire process.
First, this substance may have specific chemical activity, so it needs to be cleared, dry and good. Do not put oxidized, acid, and other substances in the same room, so as not to breed strong chemical reactions and endanger safety. Due to its nature, if exposed to moisture, it is feared that the reaction such as hydrolysis will cause the product to suffer.
There are also many conditions that need to be observed. The container must be tightly sealed to prevent leakage. In this way, it is necessary to fully consider the dangerous characteristics of this object. If it is flammable, it should be equipped with fire equipment, and the road should be avoided in densely populated and important places.
In addition, if it does not exist or does not exist, it should be well-known to all people. Familiar with the characteristics, hazards and emergency measures of this object. In the event of an accident such as leakage, it can quickly follow the established emergency case and take proper measures, such as isolation, evacuation, collection of leakage, etc., to minimize the harm.
Therefore, the storage of 3- (1-methylphenyl) naphthalene requires comprehensive consideration of the environment, containers, people, etc., and the relevant operating procedures are followed in order to ensure the safety of the entire process.
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