Linshang Chemical
PRODUCTS
[(1E)-3-Chloroprop-1-En-1-Yl]Benzene
Linshang Chemical
|
HS Code |
917143 |
| Name | [(1E)-3-Chloroprop-1-en-1-yl]Benzene |
| Molecular Formula | C9H9Cl |
| Molar Mass | 152.62 g/mol |
| Appearance | Unknown (usually a liquid or solid depending on conditions) |
| Boiling Point | Unknown |
| Melting Point | Unknown |
| Density | Unknown |
| Solubility In Water | Low (organic compound, likely insoluble in water) |
| Solubility In Organic Solvents | Good solubility in common organic solvents like ethanol, ether, etc. |
| Flash Point | Unknown |
| Vapor Pressure | Unknown |
| Chemical Reactivity | Can participate in addition and substitution reactions due to double bond and aromatic ring |
As an accredited [(1E)-3-Chloroprop-1-En-1-Yl]Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of [(1E)-3 - chloroprop - 1 - en - 1 - yl]benzene in a sealed, labeled chemical bottle. |
| Storage | [(1E)-3 - chloroprop - 1 - en - 1 - yl]benzene should be stored in a cool, dry, well - ventilated area away from heat and ignition sources. It should be kept in a tightly sealed container, preferably made of corrosion - resistant materials. Store it separately from oxidizing agents and reactive chemicals to prevent potential reactions. Label the storage container clearly with relevant safety information. |
| Shipping | [(1E)-3 - chloroprop - 1 - en - 1 - yl]benzene is shipped in well - sealed, corrosion - resistant containers. It's transported following strict chemical shipping regulations, ensuring safety during transit to prevent spills and exposure. |
Competitive [(1E)-3-Chloroprop-1-En-1-Yl]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
![[(1E)-3-Chloroprop-1-En-1-Yl]Benzene](https://alchemist-1317689233.cos.ap-nanjing.myqcloud.com/0f33e070-f267-4eb9-a4e0-654ccc03c1b5/images/product_inner1.jpg)
![[(1E)-3-Chloroprop-1-En-1-Yl]Benzene](https://alchemist-1317689233.cos.ap-nanjing.myqcloud.com/0f33e070-f267-4eb9-a4e0-654ccc03c1b5/images/product_inner2.jpg)
Where to Buy [(1E)-3-Chloroprop-1-En-1-Yl]Benzene in China?
As a trusted [(1E)-3-Chloroprop-1-En-1-Yl]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 [(1E)-3-Chloroprop-1-En-1-Yl]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 this compound [ (1E) -3-chloropropane-1-ene-1-yl] benzene
(This is a compound of (1E) -3 -chloropropane-1-alcohol-1-group) The chemical properties of this compound are as follows:
The first to bear the brunt, because it contains hydroxyl (-OH), has the typical properties of alcohols. The oxygen atom in the hydroxyl group is quite electronegative, the O-H bond polarity is very strong, and the hydrogen atom is more active. Therefore, the compound can react with active metals, such as sodium, to release hydrogen, just like the ancient wise men opened the door to material change with subtle methods, such as "2R - OH + 2Na → 2R - ONa + H ² ↑". This reaction is the paradigm of alcohol and metal reaction, just like a classic play on the chemical reaction stage.
Furthermore, the hydroxyl group can undergo a substitution reaction. When exposed to hydrohalic acid, the hydroxyl group will be replaced by a halogen atom. If it reacts with hydrobromic acid, halogenated hydrocarbons can be obtained. The process is like a clever substitution game between atoms. The reaction formula is "R-OH + HBr → R-Br + H 2O O". In this reaction, each atom changes positions in an orderly manner according to the laws of chemistry to form new substances.
Because it contains chlorine atoms, it also has the characteristics of halogenated hydrocarbons. Under basic conditions, chlorine atoms can undergo hydrolysis reactions, and chlorine atoms are replaced by hydroxyl groups, which is like an atomic "transformation" technique. The reaction is as follows: "R-Cl + NaOH → R-OH + NaCl". In a suitable alkaline environment, chlorine atoms are quietly converted into hydroxyl groups, which changes the structure and properties of the compound.
At the same time, the compound may be able to participate in the elimination reaction. If the conditions are suitable, the hydroxyl groups on the adjacent carbon atoms in the molecule combine with chlorine atoms, or with hydrogen atoms on the adjacent carbon atoms, and remove small molecules (such as water and hydrogen chloride) to form unsaturated bonds. This process is like a phoenix nirvana, and the compound is rearranged to obtain new unsaturated properties, opening a new journey of chemical change.
In addition, the interaction between the atoms in the molecule makes the chemical properties of the compound more diverse and diverse. Under different reaction conditions and reagents, it can exhibit a variety of chemical reaction paths and products, just like a constantly changing chemical picture, waiting for explorers to uncover its mysteries with wisdom and practice.
The first to bear the brunt, because it contains hydroxyl (-OH), has the typical properties of alcohols. The oxygen atom in the hydroxyl group is quite electronegative, the O-H bond polarity is very strong, and the hydrogen atom is more active. Therefore, the compound can react with active metals, such as sodium, to release hydrogen, just like the ancient wise men opened the door to material change with subtle methods, such as "2R - OH + 2Na → 2R - ONa + H ² ↑". This reaction is the paradigm of alcohol and metal reaction, just like a classic play on the chemical reaction stage.
Furthermore, the hydroxyl group can undergo a substitution reaction. When exposed to hydrohalic acid, the hydroxyl group will be replaced by a halogen atom. If it reacts with hydrobromic acid, halogenated hydrocarbons can be obtained. The process is like a clever substitution game between atoms. The reaction formula is "R-OH + HBr → R-Br + H 2O O". In this reaction, each atom changes positions in an orderly manner according to the laws of chemistry to form new substances.
Because it contains chlorine atoms, it also has the characteristics of halogenated hydrocarbons. Under basic conditions, chlorine atoms can undergo hydrolysis reactions, and chlorine atoms are replaced by hydroxyl groups, which is like an atomic "transformation" technique. The reaction is as follows: "R-Cl + NaOH → R-OH + NaCl". In a suitable alkaline environment, chlorine atoms are quietly converted into hydroxyl groups, which changes the structure and properties of the compound.
At the same time, the compound may be able to participate in the elimination reaction. If the conditions are suitable, the hydroxyl groups on the adjacent carbon atoms in the molecule combine with chlorine atoms, or with hydrogen atoms on the adjacent carbon atoms, and remove small molecules (such as water and hydrogen chloride) to form unsaturated bonds. This process is like a phoenix nirvana, and the compound is rearranged to obtain new unsaturated properties, opening a new journey of chemical change.
In addition, the interaction between the atoms in the molecule makes the chemical properties of the compound more diverse and diverse. Under different reaction conditions and reagents, it can exhibit a variety of chemical reaction paths and products, just like a constantly changing chemical picture, waiting for explorers to uncover its mysteries with wisdom and practice.
What are the physical properties of [ (1E) -3-chloropropane-1-ene-1-yl] benzene?
(1) This substance is named (1E) -3-bromopropene-1-alkyne-1-ylbenzene, and its physical properties are as follows:
Under normal conditions, (1E) -3-bromopropene-1-alkyne-1-ylbenzene is a colorless to light yellow liquid with a special odor. Its relative density is greater than that of water at room temperature and pressure. If it is placed in water, it will sink to the bottom of the water. The substance has a low melting point and is liquid at room temperature, while the boiling point will vary depending on specific conditions, but it is roughly within a certain temperature range, which allows it to vaporize when properly heated.
(1E) - 3-bromopropene-1-alkyne-1-ylbenzene is insoluble in water, but it can be miscible with some organic solvents, such as ethanol, ether, chloroform, etc. in a certain proportion. This is because its molecular structure, the properties of benzene ring, alkynyl group and bromine atom determine that it is difficult to form a good interaction with water molecules, and the force between organic solvent molecules is strong, so it is easily soluble in organic solvents.
In addition, it has a certain volatility, which will gradually evaporate in an open environment and emit its special smell. Its vapor is heavier than air and will spread close to the ground. Because it contains functional groups such as bromine atoms and alkynyl groups, these functional groups endow it with specific reactivity, and also affect physical properties to a certain extent. Optical properties such as its refractive index also have unique characteristics. Under the action of light, it will exhibit specific refraction and reflection phenomena.
Under normal conditions, (1E) -3-bromopropene-1-alkyne-1-ylbenzene is a colorless to light yellow liquid with a special odor. Its relative density is greater than that of water at room temperature and pressure. If it is placed in water, it will sink to the bottom of the water. The substance has a low melting point and is liquid at room temperature, while the boiling point will vary depending on specific conditions, but it is roughly within a certain temperature range, which allows it to vaporize when properly heated.
(1E) - 3-bromopropene-1-alkyne-1-ylbenzene is insoluble in water, but it can be miscible with some organic solvents, such as ethanol, ether, chloroform, etc. in a certain proportion. This is because its molecular structure, the properties of benzene ring, alkynyl group and bromine atom determine that it is difficult to form a good interaction with water molecules, and the force between organic solvent molecules is strong, so it is easily soluble in organic solvents.
In addition, it has a certain volatility, which will gradually evaporate in an open environment and emit its special smell. Its vapor is heavier than air and will spread close to the ground. Because it contains functional groups such as bromine atoms and alkynyl groups, these functional groups endow it with specific reactivity, and also affect physical properties to a certain extent. Optical properties such as its refractive index also have unique characteristics. Under the action of light, it will exhibit specific refraction and reflection phenomena.
What are the applications of [ (1E) -3-chloropropane-1-ene-1-yl] benzene in organic synthesis?
[ (1E) -3-chloropropane-1-ol-1-yl] silicon has many applications in organic synthesis. It can be used to prepare various functional silicone compounds.
In the field of creating silicone materials, [ (1E) -3-chloropropane-1-ol-1-yl] silicon is often used as a key raw material. Because of its unique chemical structure, it can be formed by a series of reactions, such as condensation with compounds containing active hydrogen, to generate silicone polymers with different chain lengths and functional groups. Such polymers are widely used in coatings, adhesives, sealing materials and many other industrial products, which can effectively improve the weather resistance, chemical resistance and mechanical properties of products.
In the field of medicinal chemistry, the silicon compound can act as an important synthetic intermediate. By chemically modifying it, specific pharmacoactive groups are introduced to prepare organosilicon drugs with potential biological activities. For example, by rationally designing and modifying the organic groups connected to silicon atoms, the lipophilicity, water solubility and interaction with biological targets of drug molecules can be adjusted, opening up a new path for the development of new drugs.
In organic synthesis chemistry, [ (1E) -3-chloropropane-1-alcohol-1-yl] silicon can participate in many organic reactions. For example, in transition metal-catalyzed coupling reactions, it can be used as a nucleophile or electrophilic reagent to react with other organic halides, olefins and other substrates to construct complex carbon-silicon bonds or carbon-carbon bonds, providing an effective method for the synthesis of organic compounds with diverse structures, and assisting in the synthesis of natural product analogs or new organic materials with special structures and functions.
In the field of creating silicone materials, [ (1E) -3-chloropropane-1-ol-1-yl] silicon is often used as a key raw material. Because of its unique chemical structure, it can be formed by a series of reactions, such as condensation with compounds containing active hydrogen, to generate silicone polymers with different chain lengths and functional groups. Such polymers are widely used in coatings, adhesives, sealing materials and many other industrial products, which can effectively improve the weather resistance, chemical resistance and mechanical properties of products.
In the field of medicinal chemistry, the silicon compound can act as an important synthetic intermediate. By chemically modifying it, specific pharmacoactive groups are introduced to prepare organosilicon drugs with potential biological activities. For example, by rationally designing and modifying the organic groups connected to silicon atoms, the lipophilicity, water solubility and interaction with biological targets of drug molecules can be adjusted, opening up a new path for the development of new drugs.
In organic synthesis chemistry, [ (1E) -3-chloropropane-1-alcohol-1-yl] silicon can participate in many organic reactions. For example, in transition metal-catalyzed coupling reactions, it can be used as a nucleophile or electrophilic reagent to react with other organic halides, olefins and other substrates to construct complex carbon-silicon bonds or carbon-carbon bonds, providing an effective method for the synthesis of organic compounds with diverse structures, and assisting in the synthesis of natural product analogs or new organic materials with special structures and functions.
What are the synthesis methods of [ (1E) -3-chloropropane-1-ene-1-yl] benzene
(1) The method of synthesis is very complicated, and it needs to be carefully done according to the ancient method. To make this thing, you should first prepare all kinds of materials. The important ones are (1E) -3-bromopropane, 1-aldehyde, 1-base, etc. When the amount of each thing is accurately weighed, there should be no slight difference.
(2) When the materials are ready, it is time to enter the reaction process. In the clean kettle, first add an appropriate amount of solvent to make the environment warm and appropriate, and then pour the materials in sequence. When pouring (1E) -3-bromopropane, it needs to be slow and even, like a spring rain moisturizing the product, not violent. Then, add 1-aldehyde, during which the control of the heat is very important, it is appropriate to use a low fire temperature to make the things in the kettle react harmoniously, just like the harmony of yin and yang, and the mutual growth is mutual.
(3) During the reaction, it is necessary to check carefully to observe the changes in its color and temperature. If the temperature is too high, the things in the kettle may be like a runaway horse, overreacting and causing the product to be impure; if the temperature is too low, the reaction will be slow, like water in cold winter, stagnant. Therefore, the temperature must be kept constant in a suitable range to ensure a smooth reaction.
(4) When the reaction is approaching the end, it can be seen that there is a gradual change in the kettle, or color change, or quality condensation. At this time, it is necessary to separate the product by a delicate method. Or use the technique of distillation to separate the product from the residue according to the difference in boiling point; or use the method of extraction to take the required thing by the nature of the solvent. After separation, it is purified again to remove its impurities, so that the product is pure and flawless, and then it is the finished product.
In short, the synthesis of this (1E) -3-bromopropane-1-aldehyde-1-based drug is a matter of success or failure. It requires the heart of a craftsman, based on ancient methods, and careful.
(2) When the materials are ready, it is time to enter the reaction process. In the clean kettle, first add an appropriate amount of solvent to make the environment warm and appropriate, and then pour the materials in sequence. When pouring (1E) -3-bromopropane, it needs to be slow and even, like a spring rain moisturizing the product, not violent. Then, add 1-aldehyde, during which the control of the heat is very important, it is appropriate to use a low fire temperature to make the things in the kettle react harmoniously, just like the harmony of yin and yang, and the mutual growth is mutual.
(3) During the reaction, it is necessary to check carefully to observe the changes in its color and temperature. If the temperature is too high, the things in the kettle may be like a runaway horse, overreacting and causing the product to be impure; if the temperature is too low, the reaction will be slow, like water in cold winter, stagnant. Therefore, the temperature must be kept constant in a suitable range to ensure a smooth reaction.
(4) When the reaction is approaching the end, it can be seen that there is a gradual change in the kettle, or color change, or quality condensation. At this time, it is necessary to separate the product by a delicate method. Or use the technique of distillation to separate the product from the residue according to the difference in boiling point; or use the method of extraction to take the required thing by the nature of the solvent. After separation, it is purified again to remove its impurities, so that the product is pure and flawless, and then it is the finished product.
In short, the synthesis of this (1E) -3-bromopropane-1-aldehyde-1-based drug is a matter of success or failure. It requires the heart of a craftsman, based on ancient methods, and careful.
What are the common reaction types of [ (1E) -3-chloropropane-1-ene-1-yl] benzene
In the case of (1E) -3 -alkane-1-thermal-1-group, the common reaction types are as follows:
One is the substitution reaction. This is a very typical reaction of alkanes. Take methane and chlorine as an example. Under light conditions, the hydrogen atoms in the methane molecule will be gradually replaced by chlorine atoms. The reaction process is that light prompts the chlorine-chlorine bond in the chlorine molecule to break, forming a chlorine radical (Cl ·). The chlorine radical is very active. It will capture a hydrogen atom in the methane molecule and generate hydrogen chloride and methyl radical (CH ·). The methyl radical reacts with the chlorine molecule to generate chloromethane and new chlorine radicals. In this cycle, dichloromethane, trichloromethane and carbon tetrachloride can be further generated. The essence of this reaction is the replacement of an atom or group of atoms to another atom or group of atoms.
The second is an oxidation reaction. Alkanes can burn in oxygen, which is a violent oxidation reaction. For example, ethane combustion, the chemical equation is\ (2C ² H + 7O ²\ stackrel {ignite} {=\! In this reaction, the carbon and hydrogen elements in the alkane are oxidized into carbon dioxide and water, respectively, and a large amount of heat is released at the same time, so the alkane is often used as a fuel.
The third is a cracking reaction. In a high temperature and oxygen-free or oxygen-deficient environment, the alkane molecule will break the carbon-carbon bond and carbon-hydrogen bond to form a smaller molecule of hydrocarbons. For example, when hexadecane (C H\) is cracked at high temperatures, octene (C H\) and octane (C H\) can be formed, which is of great significance to the petrochemical industry and can obtain important chemical raw materials such as ethylene and propylene.
One is the substitution reaction. This is a very typical reaction of alkanes. Take methane and chlorine as an example. Under light conditions, the hydrogen atoms in the methane molecule will be gradually replaced by chlorine atoms. The reaction process is that light prompts the chlorine-chlorine bond in the chlorine molecule to break, forming a chlorine radical (Cl ·). The chlorine radical is very active. It will capture a hydrogen atom in the methane molecule and generate hydrogen chloride and methyl radical (CH ·). The methyl radical reacts with the chlorine molecule to generate chloromethane and new chlorine radicals. In this cycle, dichloromethane, trichloromethane and carbon tetrachloride can be further generated. The essence of this reaction is the replacement of an atom or group of atoms to another atom or group of atoms.
The second is an oxidation reaction. Alkanes can burn in oxygen, which is a violent oxidation reaction. For example, ethane combustion, the chemical equation is\ (2C ² H + 7O ²\ stackrel {ignite} {=\! In this reaction, the carbon and hydrogen elements in the alkane are oxidized into carbon dioxide and water, respectively, and a large amount of heat is released at the same time, so the alkane is often used as a fuel.
The third is a cracking reaction. In a high temperature and oxygen-free or oxygen-deficient environment, the alkane molecule will break the carbon-carbon bond and carbon-hydrogen bond to form a smaller molecule of hydrocarbons. For example, when hexadecane (C H\) is cracked at high temperatures, octene (C H\) and octane (C H\) can be formed, which is of great significance to the petrochemical industry and can obtain important chemical raw materials such as ethylene and propylene.
Scan to WhatsApp
