Linshang Chemical
PRODUCTS
Benzenemethanol, 4-Chloro-2-Fluoro-
Linshang Chemical
|
HS Code |
209086 |
| Chemical Formula | C7H6ClFO |
| Molecular Weight | 160.57 |
| Appearance | Solid (likely white or off - white) |
| Solubility In Water | Low solubility, considered insoluble |
| Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, acetone, dichloromethane |
| Vapor Pressure | Low vapor pressure at room temperature |
As an accredited Benzenemethanol, 4-Chloro-2-Fluoro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 500g of 4 - chloro - 2 - fluoro - benzenemethanol in a sealed chemical - grade bottle. |
| Storage | 4 - Chloro - 2 - fluorobenzenemethanol 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, preferably made of corrosion - resistant materials like glass or certain plastics. Label the container clearly to prevent misidentification. This helps maintain its stability and reduces risks of decomposition or hazardous reactions. |
| Shipping | 4 - chloro - 2 - fluorobenzenemethanol is a chemical. Shipping requires proper packaging in accordance with regulations for chemicals. It should be labeled clearly and transported by carriers licensed for such substances to ensure safety. |
Competitive Benzenemethanol, 4-Chloro-2-Fluoro- 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 Benzenemethanol, 4-Chloro-2-Fluoro- in China?
As a trusted Benzenemethanol, 4-Chloro-2-Fluoro- manufacturer, we deliver:
Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements.
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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 Benzenemethanol, 4-Chloro-2-Fluoro- 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 4-chloro-2-fluorobenzyl alcohol?
4-Bromo-2-chloroacetophenone is also an organic compound. Its chemical properties are particularly important and are related to the basis of many chemical reactions and applications.
In this compound, bromine and chlorine atoms have significant electronegativity, which causes the electron cloud density of the benzene ring to change, making the activity of the electrophilic substitution reaction of the benzene ring different from usual. Generally speaking, due to the electron-absorbing effect of halogen atoms, the electron cloud density of the benzene ring decreases, and the activity of the electrophilic substitution reaction decreases, so the localization effect exists. Bromine and chlorine are ortho-para-sites, and the electrophilic reagents attack the ortho-and para-sites of the benzene ring more, which is the key characteristic of the electrophilic substitution reaction of aromatic incense.
Because of its carbonyl content, carbonyl has strong polarity, and has many typical reactions of carbonyl compounds. Carbonyl carbons are positively charged, vulnerable to attack by nucleophilic reagents, and nucleophilic addition reactions can occur. In case of alcohols, under the catalysis of acids or bases, ketal or semi-ketal compounds can be formed; in case of Grignard reagents, the carbon-magnesium bonds in Grignard reagents are strongly polar, carbon is negatively charged, attacking carbonyl carbons, and alcohol compounds can be obtained by hydrolysis.
And the activity of bromine and chlorine atoms in the molecule is also high, which can participate in nucleophilic substitution reactions. Under appropriate conditions, bromine and chlorine atoms can be replaced by other nucleophilic groups, such as hydroxyl groups, amino groups, etc., to synthesize organic compounds with more complex structures. Due to the above chemical properties, this compound is widely used in many fields such as medicine, pesticides, materials, etc., and can be used as key intermediates to assist in the synthesis of compounds with specific biological activities or functions.
In this compound, bromine and chlorine atoms have significant electronegativity, which causes the electron cloud density of the benzene ring to change, making the activity of the electrophilic substitution reaction of the benzene ring different from usual. Generally speaking, due to the electron-absorbing effect of halogen atoms, the electron cloud density of the benzene ring decreases, and the activity of the electrophilic substitution reaction decreases, so the localization effect exists. Bromine and chlorine are ortho-para-sites, and the electrophilic reagents attack the ortho-and para-sites of the benzene ring more, which is the key characteristic of the electrophilic substitution reaction of aromatic incense.
Because of its carbonyl content, carbonyl has strong polarity, and has many typical reactions of carbonyl compounds. Carbonyl carbons are positively charged, vulnerable to attack by nucleophilic reagents, and nucleophilic addition reactions can occur. In case of alcohols, under the catalysis of acids or bases, ketal or semi-ketal compounds can be formed; in case of Grignard reagents, the carbon-magnesium bonds in Grignard reagents are strongly polar, carbon is negatively charged, attacking carbonyl carbons, and alcohol compounds can be obtained by hydrolysis.
And the activity of bromine and chlorine atoms in the molecule is also high, which can participate in nucleophilic substitution reactions. Under appropriate conditions, bromine and chlorine atoms can be replaced by other nucleophilic groups, such as hydroxyl groups, amino groups, etc., to synthesize organic compounds with more complex structures. Due to the above chemical properties, this compound is widely used in many fields such as medicine, pesticides, materials, etc., and can be used as key intermediates to assist in the synthesis of compounds with specific biological activities or functions.
What are the physical properties of 4-chloro-2-fluorobenzyl alcohol?
4-Bromo-2-chlorotoluenitrile is an organic compound, and its physical properties are as follows:
In terms of appearance, it is mostly in solid form at room temperature, with a white to light yellow color, or nearly colorless when the texture is pure. This appearance characteristic is conducive to observation and identification in practical applications.
Melting point is an important physical constant. The melting point of 4-bromo-2-chlorotoluenitrile is in a specific temperature range. The melting point value is of great significance to its phase change under different temperature environments. In the synthesis, separation and purification process, the phase transformation and separation of compounds can be realized by suitable heating or cooling methods according to the melting point characteristics. The boiling point of the compound is also critical. The boiling point of the compound also has a specific range. The boiling point determines the limit of its conversion from liquid to gaseous state when heated to a certain temperature. In separation operations such as distillation, the difference in boiling point can be used to separate it from the mixture.
In terms of solubility, 4-bromo-2-chlorotoluonitrile exhibits a certain solubility in organic solvents. It can be dissolved in common organic solvents such as ethanol, ether, and dichloromethane, but it has poor solubility in water. This property is extremely important in organic synthesis and reaction operations. Since most organic reactions are carried out in organic solvents, good solubility ensures that it is uniformly dispersed in the reaction system, which is conducive to the full occurrence of the reaction.
Density is the mass per unit volume. The density of 4-bromo-2-chlorotoluenitrile has a specific value. When it comes to solution preparation, separation and storage, the density parameter is of great significance for determining the amount of substances and the conditions of phase separation.
In addition, 4-bromo-2-chlorotoluenitrile has certain stability, but under specific conditions, such as high temperature, strong acid, strong alkali environment, or chemical reaction, the stability determines its storage conditions and use range. Its physical properties are closely related to its structure. The bromine, chlorine atoms and nitrile groups in the molecule give it unique physical and chemical properties, which have far-reaching impact on its application in organic synthesis, medicinal chemistry and other fields.
In terms of appearance, it is mostly in solid form at room temperature, with a white to light yellow color, or nearly colorless when the texture is pure. This appearance characteristic is conducive to observation and identification in practical applications.
Melting point is an important physical constant. The melting point of 4-bromo-2-chlorotoluenitrile is in a specific temperature range. The melting point value is of great significance to its phase change under different temperature environments. In the synthesis, separation and purification process, the phase transformation and separation of compounds can be realized by suitable heating or cooling methods according to the melting point characteristics. The boiling point of the compound is also critical. The boiling point of the compound also has a specific range. The boiling point determines the limit of its conversion from liquid to gaseous state when heated to a certain temperature. In separation operations such as distillation, the difference in boiling point can be used to separate it from the mixture.
In terms of solubility, 4-bromo-2-chlorotoluonitrile exhibits a certain solubility in organic solvents. It can be dissolved in common organic solvents such as ethanol, ether, and dichloromethane, but it has poor solubility in water. This property is extremely important in organic synthesis and reaction operations. Since most organic reactions are carried out in organic solvents, good solubility ensures that it is uniformly dispersed in the reaction system, which is conducive to the full occurrence of the reaction.
Density is the mass per unit volume. The density of 4-bromo-2-chlorotoluenitrile has a specific value. When it comes to solution preparation, separation and storage, the density parameter is of great significance for determining the amount of substances and the conditions of phase separation.
In addition, 4-bromo-2-chlorotoluenitrile has certain stability, but under specific conditions, such as high temperature, strong acid, strong alkali environment, or chemical reaction, the stability determines its storage conditions and use range. Its physical properties are closely related to its structure. The bromine, chlorine atoms and nitrile groups in the molecule give it unique physical and chemical properties, which have far-reaching impact on its application in organic synthesis, medicinal chemistry and other fields.
In which fields is 4-chloro-2-fluorobenzyl alcohol used?
4-Alkane-2-alkenyl methyl ether is useful in many fields.
In the field of medicine, this compound can be used as an intermediary for pharmaceutical synthesis. It has a unique structure and specific chemical activity. It can be introduced into the drug molecular structure through various chemical reactions, thereby endowing the drug with specific biological activity and pharmacological efficacy. For example, in the synthesis pathway of some antiviral and anti-tumor drugs, 4-alkane-2-alkenyl methyl ether can ingeniously participate in the reaction, providing a key structural unit for the construction of drug activity centers, helping to optimize the performance of drug molecules and improve their therapeutic effect on diseases.
In the fragrance industry, 4-alkane-2-alkenyl methyl ether is also very popular. Because of its unique odor characteristics, it can be used to prepare a variety of fragrances. The aroma it emits may be fresh and elegant, or rich and fragrant, which can add a different flavor and layer to the fragrance. In the fragrance formulas of perfumes, air fresheners, detergents and other products, adding this compound in moderation can create a unique and pleasant aroma atmosphere and enhance the attractiveness and market competitiveness of the product.
In the field of organic synthesis chemistry, 4-alkane-2-alkenyl methyl ether is an extremely important synthetic building block. With the active functional groups such as alkenyl and methoxy groups it contains, various organic compounds with complex structures can be constructed through various classical organic reactions such as addition, substitution, and oxidation. Chemists often use this as a starting material to carefully design and implement complex synthetic routes to obtain target products with special functions or structures, and promote the continuous development and innovation of organic synthetic chemistry.
In materials science, 4-alkane-2-alkenyl methyl ethers can be used as functional monomers to participate in the polymerization of polymer materials. After polymerization, their structural units are integrated into the polymer chain, giving the material unique physical and chemical properties. For example, it may enhance the flexibility, solubility, or adsorption of materials to specific substances, thus expanding the application range of polymer materials in packaging, coatings, separation membranes, and many other fields.
In the field of medicine, this compound can be used as an intermediary for pharmaceutical synthesis. It has a unique structure and specific chemical activity. It can be introduced into the drug molecular structure through various chemical reactions, thereby endowing the drug with specific biological activity and pharmacological efficacy. For example, in the synthesis pathway of some antiviral and anti-tumor drugs, 4-alkane-2-alkenyl methyl ether can ingeniously participate in the reaction, providing a key structural unit for the construction of drug activity centers, helping to optimize the performance of drug molecules and improve their therapeutic effect on diseases.
In the fragrance industry, 4-alkane-2-alkenyl methyl ether is also very popular. Because of its unique odor characteristics, it can be used to prepare a variety of fragrances. The aroma it emits may be fresh and elegant, or rich and fragrant, which can add a different flavor and layer to the fragrance. In the fragrance formulas of perfumes, air fresheners, detergents and other products, adding this compound in moderation can create a unique and pleasant aroma atmosphere and enhance the attractiveness and market competitiveness of the product.
In the field of organic synthesis chemistry, 4-alkane-2-alkenyl methyl ether is an extremely important synthetic building block. With the active functional groups such as alkenyl and methoxy groups it contains, various organic compounds with complex structures can be constructed through various classical organic reactions such as addition, substitution, and oxidation. Chemists often use this as a starting material to carefully design and implement complex synthetic routes to obtain target products with special functions or structures, and promote the continuous development and innovation of organic synthetic chemistry.
In materials science, 4-alkane-2-alkenyl methyl ethers can be used as functional monomers to participate in the polymerization of polymer materials. After polymerization, their structural units are integrated into the polymer chain, giving the material unique physical and chemical properties. For example, it may enhance the flexibility, solubility, or adsorption of materials to specific substances, thus expanding the application range of polymer materials in packaging, coatings, separation membranes, and many other fields.
What is the preparation method of 4-chloro-2-fluorobenzyl alcohol?
To make 4-% tritium-2-deuterium bromoethane, you can follow the following ancient methods.
Prepare all kinds of materials and utensils first. An appropriate amount of deuterated ethanol and sufficient amount of sodium bromide are required, as well as concentrated sulfuric acid. A flask, a condenser tube, a separator funnel, a distillation device, etc. should also be prepared, and they all need to be clean and dry.
In the flask, mix deuterated ethanol and sodium bromide in an appropriate proportion. Slowly add concentrated sulfuric acid and stir slowly while adding. This process should be careful to prevent violent reactions. After adding, connect the flask to the condenser tube properly to ensure a good seal.
Slowly heat the flask over low heat to make the mixture evenly heated. The reaction begins, and it can be seen that there are bubbles escaping from the flask, and the liquid gradually becomes slightly boiling. During the reaction process, close attention should be paid to temperature changes and reaction phenomena, so as not to cause side reactions to breed due to excessive temperature.
After passing through, the gas generated by the reaction is cooled by a condenser and flows into the collection container. This product is mixed with many impurities, so it needs to be further purified.
The resulting product is moved to a separation funnel and washed with an appropriate amount of water to remove soluble impurities. After that, it is washed with a sodium bicarbonate solution to neutralize the remaining acid. Repeat the washing several times until the washing liquid is neutral.
Then dry the product with anhydrous calcium chloride to remove the remaining moisture. After the drying is completed, the product is moved to the distillation unit for distillation operation. Collect the fraction in a specific temperature range, which is pure 4-% tritium-2-deuterium bromoethane.
Throughout the preparation process, strict operating procedures must be followed to ensure the purity and yield of the obtained product.
Prepare all kinds of materials and utensils first. An appropriate amount of deuterated ethanol and sufficient amount of sodium bromide are required, as well as concentrated sulfuric acid. A flask, a condenser tube, a separator funnel, a distillation device, etc. should also be prepared, and they all need to be clean and dry.
In the flask, mix deuterated ethanol and sodium bromide in an appropriate proportion. Slowly add concentrated sulfuric acid and stir slowly while adding. This process should be careful to prevent violent reactions. After adding, connect the flask to the condenser tube properly to ensure a good seal.
Slowly heat the flask over low heat to make the mixture evenly heated. The reaction begins, and it can be seen that there are bubbles escaping from the flask, and the liquid gradually becomes slightly boiling. During the reaction process, close attention should be paid to temperature changes and reaction phenomena, so as not to cause side reactions to breed due to excessive temperature.
After passing through, the gas generated by the reaction is cooled by a condenser and flows into the collection container. This product is mixed with many impurities, so it needs to be further purified.
The resulting product is moved to a separation funnel and washed with an appropriate amount of water to remove soluble impurities. After that, it is washed with a sodium bicarbonate solution to neutralize the remaining acid. Repeat the washing several times until the washing liquid is neutral.
Then dry the product with anhydrous calcium chloride to remove the remaining moisture. After the drying is completed, the product is moved to the distillation unit for distillation operation. Collect the fraction in a specific temperature range, which is pure 4-% tritium-2-deuterium bromoethane.
Throughout the preparation process, strict operating procedures must be followed to ensure the purity and yield of the obtained product.
What is the market prospect of 4-chloro-2-fluorobenzyl alcohol?
Today, the four seas are flat, and commerce is flourishing. Between the markets, the goods and goods are mixed. 4-Bromo-2-chlorotoluene acetaldehyde is an important raw material in the chemical industry, and its market prospects are worth exploring.
At present, the demand for these substances in the field of pharmaceutical synthesis is increasing. The way of medicine is changing with each passing day, and many new drug research and development rely on it as a foundation to form an exquisite structure. If you create antibacterial drugs or develop new analgesic drugs, you need this material to participate in the process to help build active ingredients. It is the pharmaceutical manufacturers who are very interested in buying it and promote the prosperity of their market.
Furthermore, in the field of materials science, 4-bromo-2-chlorotoluene acetaldehyde has also emerged. Such as the preparation of photoelectric materials, its unique chemistry can give specific properties to materials, or increase their electrical conductivity, or change their luminous quality. With the pursuit of innovation in the materials industry, the demand for this product is also on the rise.
However, its market scene is not completely smooth. The technology of production is related to cost and quality. If the technology is not suitable and the cost is high, the price will be difficult to drop, and the competitiveness of the market will be damaged. And environmental protection regulations are becoming more and more stringent. The production process of this product may involve the risk of pollution. If it is not properly disposed of and restricted, it will also damage the reputation of the enterprise and hinder its development.
And the market is changing, and the emergence of competing products is also a challenge. If other products can be used instead of others, and have advantages, such as low cost and convenient access, the market of 4-bromo-2-chlorotoluene acetaldehyde will inevitably be squeezed.
However, looking at the whole, with the progress of medicine and materials, the prospect of 4-bromo-2-chlorotoluene acetaldehyde is still considerable. However, the industry needs to study the techniques, control pollution and reduce costs, but also to gain insight into the market conditions, and respond to changes in competing products in order to gain an advantage in the market and enjoy long-term prosperity.
At present, the demand for these substances in the field of pharmaceutical synthesis is increasing. The way of medicine is changing with each passing day, and many new drug research and development rely on it as a foundation to form an exquisite structure. If you create antibacterial drugs or develop new analgesic drugs, you need this material to participate in the process to help build active ingredients. It is the pharmaceutical manufacturers who are very interested in buying it and promote the prosperity of their market.
Furthermore, in the field of materials science, 4-bromo-2-chlorotoluene acetaldehyde has also emerged. Such as the preparation of photoelectric materials, its unique chemistry can give specific properties to materials, or increase their electrical conductivity, or change their luminous quality. With the pursuit of innovation in the materials industry, the demand for this product is also on the rise.
However, its market scene is not completely smooth. The technology of production is related to cost and quality. If the technology is not suitable and the cost is high, the price will be difficult to drop, and the competitiveness of the market will be damaged. And environmental protection regulations are becoming more and more stringent. The production process of this product may involve the risk of pollution. If it is not properly disposed of and restricted, it will also damage the reputation of the enterprise and hinder its development.
And the market is changing, and the emergence of competing products is also a challenge. If other products can be used instead of others, and have advantages, such as low cost and convenient access, the market of 4-bromo-2-chlorotoluene acetaldehyde will inevitably be squeezed.
However, looking at the whole, with the progress of medicine and materials, the prospect of 4-bromo-2-chlorotoluene acetaldehyde is still considerable. However, the industry needs to study the techniques, control pollution and reduce costs, but also to gain insight into the market conditions, and respond to changes in competing products in order to gain an advantage in the market and enjoy long-term prosperity.
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