Linshang Chemical
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(3-Chloro-1-Propenyl)Benzene
Linshang Chemical
|
HS Code |
720906 |
| Chemical Formula | C9H9Cl |
| Molar Mass | 154.62 g/mol |
| Appearance | Liquid (usually) |
| Boiling Point | Around 200 - 205 °C |
| Density | Approx. 1.06 - 1.08 g/cm³ |
| Solubility In Water | Insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
| Flash Point | Relatively high, as it's a non - highly volatile aromatic compound |
| Odor | Aromatic odor |
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 in a sealed, corrosion - resistant container. |
| Storage | (3 - chloro - 1 - propenyl)benzene should be stored in a cool, dry, well - ventilated area away from heat sources and open flames. It should be kept in a tightly - sealed container to prevent evaporation and contamination. Since it is likely flammable, store it separate from oxidizing agents. Avoid storing in areas with high humidity to prevent potential hydrolysis reactions. |
| Shipping | (3 - chloro - 1 - propenyl)benzene is shipped in accordance with strict chemical transport regulations. It's packed in suitable containers to prevent leakage, and transported by approved carriers, ensuring safety during transit. |
Competitive (3-Chloro-1-Propenyl)Benzene prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615365006308 or mail to info@alchemist-chem.com.
We will respond to you as soon as possible.
Tel: +8615365006308
Email: info@alchemist-chem.com
Where to Buy (3-Chloro-1-Propenyl)Benzene in China?
As a trusted (3-Chloro-1-Propenyl)Benzene 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 (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?
(3-Chloro-1-propenyl) benzene is an organic compound with many unique chemical properties.
Firstly, the alkenyl group in this compound is conjugated with the benzene ring, which increases the stability of the system. The chlorine atom on the alkenyl group has an impact on the electron cloud distribution of the compound due to its electronegativity. In the electrophilic substitution reaction, the benzene ring is vulnerable to the attack of electrophilic reagents due to the relatively high electron cloud density of the conjugated system. Due to the combined effect of the electron-absorbing effect of the chlorine atom and the conjugation effect, the activity of the electrophilic substitution reaction may be slightly reduced than that of benzene, and the substitution position may be selective, and the ratio of ortho-and para-position substitution products may be different from that If it is added to halogens and hydrogen halides, it follows the Markov rule or the anti-Markov rule, depending on the reaction conditions. The alkenyl group can be hydrogenated with hydrogen under a suitable catalyst to form a saturated hydrocarbon derivative.
In addition, due to the presence of chlorine atoms, (3-chloro-1-propenyl) benzene can undergo a nucleophilic substitution reaction. The nucleophilic reagent can attack the carbon atom connected to the chlorine, and the chlorine atom leaves to form a new compound.
And because the alkenyl group is connected to the benzene ring, under certain conditions, an oxidation reaction can occur. The alkenyl group or the benzene ring can be oxidized to form a corresponding oxidation product, depending on the oxidizing agent and the reaction conditions.
In summary, the unique structure of (3-chloro-1-propenyl) benzene has diverse reactivity and application potential in the field of organic synthesis.
Firstly, the alkenyl group in this compound is conjugated with the benzene ring, which increases the stability of the system. The chlorine atom on the alkenyl group has an impact on the electron cloud distribution of the compound due to its electronegativity. In the electrophilic substitution reaction, the benzene ring is vulnerable to the attack of electrophilic reagents due to the relatively high electron cloud density of the conjugated system. Due to the combined effect of the electron-absorbing effect of the chlorine atom and the conjugation effect, the activity of the electrophilic substitution reaction may be slightly reduced than that of benzene, and the substitution position may be selective, and the ratio of ortho-and para-position substitution products may be different from that If it is added to halogens and hydrogen halides, it follows the Markov rule or the anti-Markov rule, depending on the reaction conditions. The alkenyl group can be hydrogenated with hydrogen under a suitable catalyst to form a saturated hydrocarbon derivative.
In addition, due to the presence of chlorine atoms, (3-chloro-1-propenyl) benzene can undergo a nucleophilic substitution reaction. The nucleophilic reagent can attack the carbon atom connected to the chlorine, and the chlorine atom leaves to form a new compound.
And because the alkenyl group is connected to the benzene ring, under certain conditions, an oxidation reaction can occur. The alkenyl group or the benzene ring can be oxidized to form a corresponding oxidation product, depending on the oxidizing agent and the reaction conditions.
In summary, the unique structure of (3-chloro-1-propenyl) benzene has diverse reactivity and application potential in the field of organic synthesis.
What are the physical properties of (3-chloro-1-propenyl) benzene?
(3-Chloro-1-propenyl) benzene is one of the organic compounds. Its physical properties are particularly important, and it is related to the various characteristics and applications of this compound.
In terms of its appearance, (3-chloro-1-propenyl) benzene is often colorless to light yellow liquid, clear and transparent. When viewed under light, there may be a slight flicker, like a jade liquid flowing.
Its smell is unique and has a fragrant charm. However, this fragrance is also mixed with a little irritating smell. The smell is quite impressive, as if you are in a state where a strange fragrance and a slightly prickly feeling blend.
The boiling point of (3-chloro-1-propenyl) benzene is worth noting. Under normal pressure, its boiling point is in a specific temperature range, which makes the compound gradually change from liquid to gaseous. The existence of boiling point determines its phase change under different temperature environments, which is of great significance in chemical production, separation and purification.
As for the melting point, it is also an important physical property. When the temperature drops to a certain value, (3-chloro-1-propenyl) benzene will solidify from liquid to solid. The characteristics of this melting point affect its storage and transportation conditions.
Furthermore, its density cannot be ignored. ( The density of 3-chloro-1-propenyl) benzene may be different from that of water. This property is a key consideration in liquid-liquid separation and other operations, and is related to the success or failure and efficiency of the separation process.
In terms of solubility, (3-chloro-1-propenyl) benzene in organic solvents, such as ethanol, ether, etc., often exhibits good solubility and can be mutually soluble with it, just like water emulsion. However, in water, its solubility is very small, and the two seem to be distinct. This difference in solubility is an important basis in many operations such as organic synthesis and extraction, guiding the experimenter to choose the appropriate solvent to achieve the ideal reaction or separation effect.
In terms of its appearance, (3-chloro-1-propenyl) benzene is often colorless to light yellow liquid, clear and transparent. When viewed under light, there may be a slight flicker, like a jade liquid flowing.
Its smell is unique and has a fragrant charm. However, this fragrance is also mixed with a little irritating smell. The smell is quite impressive, as if you are in a state where a strange fragrance and a slightly prickly feeling blend.
The boiling point of (3-chloro-1-propenyl) benzene is worth noting. Under normal pressure, its boiling point is in a specific temperature range, which makes the compound gradually change from liquid to gaseous. The existence of boiling point determines its phase change under different temperature environments, which is of great significance in chemical production, separation and purification.
As for the melting point, it is also an important physical property. When the temperature drops to a certain value, (3-chloro-1-propenyl) benzene will solidify from liquid to solid. The characteristics of this melting point affect its storage and transportation conditions.
Furthermore, its density cannot be ignored. ( The density of 3-chloro-1-propenyl) benzene may be different from that of water. This property is a key consideration in liquid-liquid separation and other operations, and is related to the success or failure and efficiency of the separation process.
In terms of solubility, (3-chloro-1-propenyl) benzene in organic solvents, such as ethanol, ether, etc., often exhibits good solubility and can be mutually soluble with it, just like water emulsion. However, in water, its solubility is very small, and the two seem to be distinct. This difference in solubility is an important basis in many operations such as organic synthesis and extraction, guiding the experimenter to choose the appropriate solvent to achieve the ideal reaction or separation effect.
What are the main uses of (3-chloro-1-propenyl) benzene?
(3-Chloro-1-propenyl) benzene, an organic compound, is widely used in chemical synthesis and other fields. Its main use is as an intermediate in organic synthesis. In the fine chemical synthesis path, it can be converted into other organic compounds with specific functions by many chemical reactions, such as nucleophilic substitution and addition reactions. For example, it can react with compounds containing active groups to prepare intermediates for pesticides, medicines, fragrances and other products.
Furthermore, it has applications in the field of materials science. Due to the characteristics of molecular structure, it may participate in certain polymerization reactions to prepare polymer materials with special properties, such as polymers with specific optical, electrical or mechanical properties, which can be used in electronic devices, optical materials, etc.
In addition, the chemical activity of (3-chloro-1-propenyl) benzene makes it suitable for organometallic chemistry, or it can be used as a ligand to participate in metal catalytic reactions, helping to achieve efficient synthesis of specific organic compounds and promoting the development of catalytic chemistry.
Furthermore, it has applications in the field of materials science. Due to the characteristics of molecular structure, it may participate in certain polymerization reactions to prepare polymer materials with special properties, such as polymers with specific optical, electrical or mechanical properties, which can be used in electronic devices, optical materials, etc.
In addition, the chemical activity of (3-chloro-1-propenyl) benzene makes it suitable for organometallic chemistry, or it can be used as a ligand to participate in metal catalytic reactions, helping to achieve efficient synthesis of specific organic compounds and promoting the development of catalytic chemistry.
What are the synthesis methods of (3-chloro-1-propenyl) benzene?
There are several ways to prepare (3-chloro-1-propenyl) benzene. First, it can be obtained by the alkylation of benzene with 3-chloro-1-propene through Fu-g alkylation. This reaction requires Lewis acids such as anhydrous aluminum trichloride as catalysts. Under appropriate temperatures, the hydrogen on the benzene ring is replaced by 3-chloro-1-propenyl to obtain the target product. During the reaction, attention should be paid to the control of the reaction conditions. Too high or too low temperature can affect the yield and product purity.
Second, suitable halogenated hydrocarbons, such as 1-chloro-3-iodopropene, can be prepared first, and then reacted with phenylboronic acid under palladium catalyst to synthesize (3-chloro-1-propylene-based) benzene through Suzuki. This method has relatively mild conditions and good selectivity, which can effectively reduce the occurrence of side reactions. However, palladium catalysts are expensive and require high reaction equipment and operation.
Third, it can also be added with phenylacetylene and hydrogen chloride to obtain 1-chloro-1-styrene first, and then partially hydrogenated to obtain (3-chloro-1-propenyl) benzene. The hydrogenation reduction step requires the selection of suitable catalysts and reaction conditions to ensure the selective reduction of double bonds and avoid excessive reduction to form saturated hydrocarbons.
Various synthetic methods have their own advantages and disadvantages. In practical application, the optimal method should be selected according to specific requirements, such as the availability of raw materials, cost, product purity and other factors.
Second, suitable halogenated hydrocarbons, such as 1-chloro-3-iodopropene, can be prepared first, and then reacted with phenylboronic acid under palladium catalyst to synthesize (3-chloro-1-propylene-based) benzene through Suzuki. This method has relatively mild conditions and good selectivity, which can effectively reduce the occurrence of side reactions. However, palladium catalysts are expensive and require high reaction equipment and operation.
Third, it can also be added with phenylacetylene and hydrogen chloride to obtain 1-chloro-1-styrene first, and then partially hydrogenated to obtain (3-chloro-1-propenyl) benzene. The hydrogenation reduction step requires the selection of suitable catalysts and reaction conditions to ensure the selective reduction of double bonds and avoid excessive reduction to form saturated hydrocarbons.
Various synthetic methods have their own advantages and disadvantages. In practical application, the optimal method should be selected according to specific requirements, such as the availability of raw materials, cost, product purity and other factors.
What are the precautions for (3-chloro-1-propenyl) benzene during storage and transportation?
For (3-chloro-1-propylene) benzene, there are many matters to be paid attention to during storage and transportation.
The first one concerns the storage environment. This substance should be stored in a cool and ventilated warehouse, away from fires and heat sources, to prevent dangerous reactions caused by excessive temperature. The temperature of the warehouse should be controlled within a specific range, and it must not be heated. Due to heat, it may cause its volatilization to increase, or even cause chemical reactions, endangering safety.
The second one is about packaging. The packaging must be tight to prevent leakage. The packaging material selected must be able to resist the corrosion of (3-chloro-1-propylene) benzene and have good sealing performance. If the package is damaged, (3-chloro-1-propenyl) benzene leaks out, which will not only cause material loss, but also may pollute the environment and endanger the health of surrounding people.
Furthermore, when it comes to transportation. During transportation, vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. During transportation, ensure that the container does not leak, collapse, fall or damage. Driving routes should avoid passing through sensitive areas such as densely populated areas and water source protection areas to prevent major losses in the event of accidents. Transport personnel must also undergo special training to be familiar with the characteristics and emergency treatment methods of (3-chloro-1-propylene) benzene, and always check the condition of the goods during transportation to ensure safe transportation.
In addition, (3-chloro-1-propylene) benzene may be toxic and irritating. Whether it is stored or transported, relevant operators should take appropriate protective measures, such as wearing protective gloves, protective glasses and gas masks, to avoid direct contact and inhalation to ensure their own safety.
The first one concerns the storage environment. This substance should be stored in a cool and ventilated warehouse, away from fires and heat sources, to prevent dangerous reactions caused by excessive temperature. The temperature of the warehouse should be controlled within a specific range, and it must not be heated. Due to heat, it may cause its volatilization to increase, or even cause chemical reactions, endangering safety.
The second one is about packaging. The packaging must be tight to prevent leakage. The packaging material selected must be able to resist the corrosion of (3-chloro-1-propylene) benzene and have good sealing performance. If the package is damaged, (3-chloro-1-propenyl) benzene leaks out, which will not only cause material loss, but also may pollute the environment and endanger the health of surrounding people.
Furthermore, when it comes to transportation. During transportation, vehicles should be equipped with corresponding varieties and quantities of fire-fighting equipment and leakage emergency treatment equipment. During transportation, ensure that the container does not leak, collapse, fall or damage. Driving routes should avoid passing through sensitive areas such as densely populated areas and water source protection areas to prevent major losses in the event of accidents. Transport personnel must also undergo special training to be familiar with the characteristics and emergency treatment methods of (3-chloro-1-propylene) benzene, and always check the condition of the goods during transportation to ensure safe transportation.
In addition, (3-chloro-1-propylene) benzene may be toxic and irritating. Whether it is stored or transported, relevant operators should take appropriate protective measures, such as wearing protective gloves, protective glasses and gas masks, to avoid direct contact and inhalation to ensure their own safety.
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