Linshang Chemical
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4-Chloro-2-Chloromethyl Benzenepropanol
Linshang Chemical
|
HS Code |
960682 |
| Chemical Formula | C10H12Cl2O |
| Molecular Weight | 221.11 |
| Appearance | Solid (Typical) |
| Odor | Characteristic (Typical organic chemical odor) |
| Melting Point | Specific value would need lab determination |
| Boiling Point | Specific value would need lab determination |
| Density | Specific value would need lab determination |
| Solubility In Water | Low (Typical for such organic compounds) |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone |
| Flash Point | Specific value would need lab determination |
| Vapor Pressure | Low (Typical for non - volatile solids) |
| Stability | Stable under normal conditions but may react with strong oxidants |
As an accredited 4-Chloro-2-Chloromethyl Benzenepropanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 4 - chloro - 2 - chloromethyl Benzenepropanol packaged in a sealed, chemical - resistant bottle. |
| Storage | 4 - chloro - 2 - chloromethylbenzenepropanol should be stored in a cool, dry, well - ventilated area, away from heat sources and open flames. Keep it in a tightly closed container to prevent exposure to air and moisture. Store it separately from oxidizing agents, acids, and bases to avoid potential chemical reactions. Ensure proper labeling for easy identification and to comply with safety regulations. |
| Shipping | 4 - chloro - 2 - chloromethyl Benzenepropanol should be shipped in accordance with chemical regulations. Pack it in well - sealed, corrosion - resistant containers. Clearly label with hazard warnings. Transport via approved carriers under proper safety precautions. |
Competitive 4-Chloro-2-Chloromethyl Benzenepropanol prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615365006308
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As a leading 4-Chloro-2-Chloromethyl Benzenepropanol supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.
4-chloro-2-chloromethyl the chemical structure of Benzenepropanol
4-Chloro-2-chloromethylphenylpropanol, according to its name, it can be known that it is an organic compound containing chlorine. In this compound, the benzene ring is its core skeleton, which is connected with chlorine atoms and chloromethyl groups, and the side chain is propanol structure. On the
benzene ring, there are chlorine atoms and chloromethyl groups at the 4th and 2nd positions, respectively. The chlorine atoms and chloromethyl are based on the specific positions of the benzene ring, which have a profound impact on the properties of the compound. The benzene ring has a conjugated system and its properties are stable, but the substituents on it can cause changes in the distribution of electron clouds, which in turn affect the reactivity of the compound. The propanol structure of the side chain of
< The hydroxyl group is an active functional group and can participate in many chemical reactions, such as esterification reaction and oxidation reaction. The existence of propanol side chain endows the compound with a certain hydrophilicity, because the hydroxyl group can form hydrogen bonds with water molecules.
The structure of this compound makes it both the stability of the benzene ring and the activity of the propanol side chain. The electronic effect of chlorine atoms and chloromethyl groups can affect the electron cloud density of the benzene ring and change its electrophilic substitution activity. At the same time, the hydroxyl groups of the propanol side chain can participate in a variety of organic synthesis reactions, providing the possibility for the preparation of complex organic compounds. Such a unique chemical structure makes it useful in organic synthesis, pharmaceutical chemistry and other fields.
benzene ring, there are chlorine atoms and chloromethyl groups at the 4th and 2nd positions, respectively. The chlorine atoms and chloromethyl are based on the specific positions of the benzene ring, which have a profound impact on the properties of the compound. The benzene ring has a conjugated system and its properties are stable, but the substituents on it can cause changes in the distribution of electron clouds, which in turn affect the reactivity of the compound. The propanol structure of the side chain of
< The hydroxyl group is an active functional group and can participate in many chemical reactions, such as esterification reaction and oxidation reaction. The existence of propanol side chain endows the compound with a certain hydrophilicity, because the hydroxyl group can form hydrogen bonds with water molecules.
The structure of this compound makes it both the stability of the benzene ring and the activity of the propanol side chain. The electronic effect of chlorine atoms and chloromethyl groups can affect the electron cloud density of the benzene ring and change its electrophilic substitution activity. At the same time, the hydroxyl groups of the propanol side chain can participate in a variety of organic synthesis reactions, providing the possibility for the preparation of complex organic compounds. Such a unique chemical structure makes it useful in organic synthesis, pharmaceutical chemistry and other fields.
4-chloro-2-chloromethyl the physical properties of Benzenepropanol
4-Chloro-2-chloromethylphenylpropanol is an organic compound. Its physical properties are as follows:
Looking at it, it is mostly a colorless to light yellow liquid at room temperature, with a clear appearance, like a clear spring in the mountains, and no visible impurities.
Smell it, it has a special smell, not a rich fragrance, nor a pungent smell, but its unique taste can impress the smell.
As for the melting point, the melting point is low, and it is liquid at room temperature. The boiling point is relatively high, and a considerable amount of heat is required to make it boil into a gaseous state. This is because of the force between molecules, like people pulling each other, it takes a lot of force to separate each other. In terms of solubility, in organic solvents, such as ethanol, ether, etc., the solubility is quite good, just like a fish entering water, it can be well miscible with organic solvents. However, in water, the solubility is not good, because its molecular structure and the polarity of water are quite different, and the two are difficult to blend, just like oil and water, distinct.
The density is slightly larger than that of water. If it is placed in one place with water, it will sink to the bottom like a stone.
The physical properties of this compound have far-reaching influence in many fields such as chemical industry and medicine. Due to its special physical properties, it can be used as an important intermediate in organic synthesis to help synthesize a variety of complex organic compounds, just like the cornerstone of building a tall building.
Looking at it, it is mostly a colorless to light yellow liquid at room temperature, with a clear appearance, like a clear spring in the mountains, and no visible impurities.
Smell it, it has a special smell, not a rich fragrance, nor a pungent smell, but its unique taste can impress the smell.
As for the melting point, the melting point is low, and it is liquid at room temperature. The boiling point is relatively high, and a considerable amount of heat is required to make it boil into a gaseous state. This is because of the force between molecules, like people pulling each other, it takes a lot of force to separate each other. In terms of solubility, in organic solvents, such as ethanol, ether, etc., the solubility is quite good, just like a fish entering water, it can be well miscible with organic solvents. However, in water, the solubility is not good, because its molecular structure and the polarity of water are quite different, and the two are difficult to blend, just like oil and water, distinct.
The density is slightly larger than that of water. If it is placed in one place with water, it will sink to the bottom like a stone.
The physical properties of this compound have far-reaching influence in many fields such as chemical industry and medicine. Due to its special physical properties, it can be used as an important intermediate in organic synthesis to help synthesize a variety of complex organic compounds, just like the cornerstone of building a tall building.
What are the main uses of 4-chloro-2-chloromethyl Benzenepropanol?
4-Chloro-2-chloromethylphenylpropanol, this is an organic compound. It has a wide range of uses and is often used as a key intermediate in the synthesis of medicine. Due to its unique molecular structure, with chlorine atoms, chloromethyl and phenylpropanol structures, it can use a variety of chemical reactions to build more complex medicinal molecular structures, helping to create new drugs to treat various diseases.
It is also useful in the field of materials science. By virtue of its own characteristics, or by participating in the synthesis of specific materials, it imparts excellent characteristics such as good stability, special optical or electrical properties to materials, and then meets the diverse needs of electronic, optical materials and other fields.
In the field of fine chemicals, it can be used as a starting material for the synthesis of fine chemicals such as special surfactants and fragrances. After ingenious chemical reactions, it is converted into fine chemical products with specific functions to meet the needs of different industrial and civilian scenarios.
Looking at its use, it is actually an important substance in many fields and an important substance to promote the development of related industries.
It is also useful in the field of materials science. By virtue of its own characteristics, or by participating in the synthesis of specific materials, it imparts excellent characteristics such as good stability, special optical or electrical properties to materials, and then meets the diverse needs of electronic, optical materials and other fields.
In the field of fine chemicals, it can be used as a starting material for the synthesis of fine chemicals such as special surfactants and fragrances. After ingenious chemical reactions, it is converted into fine chemical products with specific functions to meet the needs of different industrial and civilian scenarios.
Looking at its use, it is actually an important substance in many fields and an important substance to promote the development of related industries.
4-chloro-2-chloromethyl are the synthetic methods of Benzenepropanol
There are several methods for the synthesis of 4-chloro-2-chloromethylphenylpropanol as follows.
First, chlorine atoms can be introduced through halogenation from suitable starting materials. First, take the compound containing the benzene ring, and under suitable reaction conditions, treat it with a halogenating reagent, so that the hydrogen atoms at specific positions in the benzene ring are replaced by chlorine atoms, so as to obtain benzene derivatives with chlorine substituents. In this process, precise control of reaction conditions, such as temperature, reaction time and reagent dosage, is required to ensure that the chlorine atoms are introduced at the desired positions.
Next, chloromethyl is introduced into the halogenated benzene ring derivatives by specific reaction steps. This step may require the use of special reagents and catalysts to achieve the precise connection of chloromethyl based on the target position. The reaction environment is also very critical, and factors such as pH and solvent need to be carefully controlled to make the reaction proceed smoothly and avoid side reactions.
Second, another synthetic approach can be considered from phenylpropanol derivatives. First, the benzene ring part of phenylpropanol is modified, and some reactions can be used to activate the benzene ring, which is convenient for subsequent halogenation reactions. By selecting suitable halogenating agents and reaction conditions, chlorine atoms are introduced at designated positions in the benzene ring. Subsequently, chloromethyl is introduced at suitable positions in the benzene ring through specific reactions. This process also requires fine control of the reaction parameters of each step to achieve the purpose of high yield and high selectivity.
Furthermore, a strategy of combining the gradual construction of carbon chains with the introduction of functional groups can be tried. First, an intermediate with a partial carbon chain structure and reactive check point is constructed, and then chlorine atoms and chloromethyl groups are gradually introduced through a series of reactions, such as nucleophilic substitution and addition, and finally the structure of 4-chloro-2-chloromethylphenylpropanol is formed. Each step of the reaction needs to be based on the characteristics of the intermediate, and the reaction reagents, catalysts and reaction conditions should be reasonably selected to ensure the feasibility and efficiency of the synthesis route.
In conclusion, there are various methods for synthesizing 4-chloro-2-chloromethylphenylpropanol, and each method has its own advantages and disadvantages. It is necessary to carefully select and optimize the synthesis path according to actual needs and conditions to obtain satisfactory synthesis results.
First, chlorine atoms can be introduced through halogenation from suitable starting materials. First, take the compound containing the benzene ring, and under suitable reaction conditions, treat it with a halogenating reagent, so that the hydrogen atoms at specific positions in the benzene ring are replaced by chlorine atoms, so as to obtain benzene derivatives with chlorine substituents. In this process, precise control of reaction conditions, such as temperature, reaction time and reagent dosage, is required to ensure that the chlorine atoms are introduced at the desired positions.
Next, chloromethyl is introduced into the halogenated benzene ring derivatives by specific reaction steps. This step may require the use of special reagents and catalysts to achieve the precise connection of chloromethyl based on the target position. The reaction environment is also very critical, and factors such as pH and solvent need to be carefully controlled to make the reaction proceed smoothly and avoid side reactions.
Second, another synthetic approach can be considered from phenylpropanol derivatives. First, the benzene ring part of phenylpropanol is modified, and some reactions can be used to activate the benzene ring, which is convenient for subsequent halogenation reactions. By selecting suitable halogenating agents and reaction conditions, chlorine atoms are introduced at designated positions in the benzene ring. Subsequently, chloromethyl is introduced at suitable positions in the benzene ring through specific reactions. This process also requires fine control of the reaction parameters of each step to achieve the purpose of high yield and high selectivity.
Furthermore, a strategy of combining the gradual construction of carbon chains with the introduction of functional groups can be tried. First, an intermediate with a partial carbon chain structure and reactive check point is constructed, and then chlorine atoms and chloromethyl groups are gradually introduced through a series of reactions, such as nucleophilic substitution and addition, and finally the structure of 4-chloro-2-chloromethylphenylpropanol is formed. Each step of the reaction needs to be based on the characteristics of the intermediate, and the reaction reagents, catalysts and reaction conditions should be reasonably selected to ensure the feasibility and efficiency of the synthesis route.
In conclusion, there are various methods for synthesizing 4-chloro-2-chloromethylphenylpropanol, and each method has its own advantages and disadvantages. It is necessary to carefully select and optimize the synthesis path according to actual needs and conditions to obtain satisfactory synthesis results.
4-chloro-2-chloromethyl Benzenepropanol in the use of what are the precautions
4-Chloro-2-chloromethylphenylpropanol is an important organic compound that is used in many fields. However, when using it, there are indeed many points to be paid attention to, as detailed below:
Bear the brunt, and safety protection should not be ignored. This compound may be toxic and irritating, and may cause damage to the human body if it touches the skin, eyes or inhales its vapor. When operating, be sure to wear appropriate protective equipment, such as laboratory clothes, gloves and protective glasses, to avoid direct contact with it. If it is accidentally touched, immediately rinse with plenty of water and seek medical attention according to the specific situation.
Furthermore, storage conditions are also extremely critical. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because it is an organic compound, it may burn or even explode in case of open flame or hot topic. And it needs to be stored separately from oxidants, acids, etc., and must not be mixed to prevent chemical reactions.
Operating specifications during use should not be ignored. When conducting relevant reactions or experiments, it is necessary to strictly follow the established operating procedures. For example, control the reaction temperature, reaction time and the proportion of reactants to ensure that the reaction can proceed smoothly in the expected direction and avoid side reactions. In addition, the operation process needs to be completed in a fume hood to effectively discharge possible harmful gases.
In addition, waste disposal also needs to be treated with caution. For waste generated after use, it should not be discarded at will, and it must be properly disposed of in accordance with relevant environmental protection regulations. You can contact a professional waste treatment agency to ensure that waste can be disposed of in a safe and environmentally friendly manner to avoid pollution to the environment.
In summary, when using 4-chloro-2-chloromethylphenylpropanol, every link is related to experimental safety, personnel health and environmental protection. It must not be taken lightly and needs to be treated strictly.
Bear the brunt, and safety protection should not be ignored. This compound may be toxic and irritating, and may cause damage to the human body if it touches the skin, eyes or inhales its vapor. When operating, be sure to wear appropriate protective equipment, such as laboratory clothes, gloves and protective glasses, to avoid direct contact with it. If it is accidentally touched, immediately rinse with plenty of water and seek medical attention according to the specific situation.
Furthermore, storage conditions are also extremely critical. It should be stored in a cool, dry and well-ventilated place, away from fire and heat sources. Because it is an organic compound, it may burn or even explode in case of open flame or hot topic. And it needs to be stored separately from oxidants, acids, etc., and must not be mixed to prevent chemical reactions.
Operating specifications during use should not be ignored. When conducting relevant reactions or experiments, it is necessary to strictly follow the established operating procedures. For example, control the reaction temperature, reaction time and the proportion of reactants to ensure that the reaction can proceed smoothly in the expected direction and avoid side reactions. In addition, the operation process needs to be completed in a fume hood to effectively discharge possible harmful gases.
In addition, waste disposal also needs to be treated with caution. For waste generated after use, it should not be discarded at will, and it must be properly disposed of in accordance with relevant environmental protection regulations. You can contact a professional waste treatment agency to ensure that waste can be disposed of in a safe and environmentally friendly manner to avoid pollution to the environment.
In summary, when using 4-chloro-2-chloromethylphenylpropanol, every link is related to experimental safety, personnel health and environmental protection. It must not be taken lightly and needs to be treated strictly.
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