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Product Name | 4-Chlorophenyl acrylic acid |
Cas Number | 1522-92-5 |
Formula | C9H7ClO2 |
Molar Mass | 182.6 |
Property1 | Melting point: 102-105°C |
Property2 | Boiling point: 194°C (at 20 mmHg) |
Property3 | Solubility: Slightly soluble in water |
Property4 | Density: 1.34 g/cm³ |
Property5 | Appearance: White to off-white crystalline powder |
Property6 | pKa: 4.31 |
Property7 | Flash point: 88°C |
Property8 | Refractive index: 1.579 |
Property9 | Stability: Stable under normal temperatures and pressures |
Property10 | Storage conditions: Store in a cool, dry place |
What is the application of 4-Chlorophenylacrylic acid?
4 - Chlorophenylacrylic acid has several applications in different fields.The chlorophenylacrylic acids has many applications in different fields.
In the pharmaceutical industry, it serves as an important intermediate.It is an important intermediate in the pharmaceutical industry. Its unique chemical structure allows it to be a key building block for the synthesis of various drugs.Its unique chemistry makes it a valuable building block in the synthesis of many drugs. For example, some anti - inflammatory and analgesic drugs may utilize 4 - Chlorophenylacrylic acid in their synthetic routes.Some anti-inflammatory and analgesic medications may use 4 - chlorophenylacrylic acids in their syntheses. The chlorine atom and the acrylic acid moiety can participate in chemical reactions to form more complex molecules with specific biological activities.The acrylic acid moiety and the chlorine atom can be involved in chemical reactions that produce more complex molecules with different biological activities. The acid group can be modified to form esters or amides, which may enhance the drug's solubility, bioavailability, or target - binding affinity.The acid group may be modified to form esters and amides that can enhance the drug's bioavailability or target-binding affinity.
In the agrochemical field, 4 - Chlorophenylacrylic acid can be used in the development of pesticides and herbicides.In the agrochemical industry, 4 - chlorophenylacrylic can be used to develop pesticides and herbalicides. Its chemical properties enable it to interact with specific biological targets in pests or weeds.Its chemical properties allow it to interact with specific targets in pests and weeds. For instance, it may disrupt certain metabolic pathways in these organisms.It may, for example, disrupt certain metabolic pathways within these organisms. The presence of the chlorine atom can enhance its lipophilicity, allowing it to penetrate the cell membranes of pests or weeds more effectively.The presence of a chlorine atom can increase its lipophilicity. This allows it to penetrate cell membranes more effectively. This can lead to the inhibition of growth, reproduction, or even death of these unwanted organisms, thus protecting crops.This can result in the inhibition of growth or reproduction of unwanted organisms.
In the area of materials science, 4 - Chlorophenylacrylic acid can contribute to the synthesis of specialty polymers.In the field of materials science, 4-Chlorophenylacrylic Acid can be used to synthesize specialty polymers. It can be polymerized with other monomers to create polymers with unique properties.It can be polymerized to create polymers that have unique properties. The chlorine - containing phenyl group can influence the polymer's physical and chemical properties, such as thermal stability, mechanical strength, and chemical resistance.The phenyl group containing chlorine can affect the polymer's chemical and physical properties, including thermal stability, mechanical resistance, and chemical resistant. These polymers may find applications in coatings, adhesives, or high - performance plastics.These polymers can be used in coatings or adhesives as well as high-performance plastics. For example, in coatings, the resulting polymer can provide better protection against environmental factors like moisture, UV radiation, and chemical corrosion due to the characteristics imparted by 4 - Chlorophenylacrylic acid.The characteristics of 4 - chlorophenylacrylic acids can be used to improve the protection provided by the polymer in coatings against environmental factors such as moisture, UV radiation and chemical corrosion.
In addition, 4 - Chlorophenylacrylic acid can also be used in research laboratories as a standard or reference compound.4 - Chlorophenylacrylic Acid can be used as a reference or standard compound in research laboratories. Scientists can use it to study chemical reactions, reaction mechanisms, and to validate analytical methods.Scientists can use this compound to study chemical reactions and reaction mechanisms as well as to validate analytical methods. Its well - defined structure and known properties make it a useful tool for understanding the behavior of similar compounds and for developing new synthetic strategies.Its well-defined structure and known properties are useful for understanding the behavior and developing new synthetic strategies of similar compounds. Overall, 4 - Chlorophenylacrylic acid plays a significant role in multiple industries due to its versatile chemical reactivity and unique structural features.The versatility of its chemical reactivity, as well as its unique structural features, make 4 - chlorophenylacrylic an important player in many industries.
What are the properties of 4-Chlorophenylacrylic acid?
4 - Chlorophenylacrylic acid has several notable properties.The properties of chlorophenylacrylic acids are quite remarkable.
Physical Properties
In terms of appearance, 4 - Chlorophenylacrylic acid is typically a solid.4 - Chlorophenylacrylic Acid is usually a solid. It has a defined melting point, which is around 172 - 174 degC.It has a defined melt point of 172-174 degC. This relatively high melting point is characteristic of many organic acids with a planar and rigid molecular structure.This relatively high melting temperature is characteristic of many acids with a rigid and planar molecular structure. The compound's solid - state form at room temperature is due to the presence of strong intermolecular forces, such as hydrogen bonding between the carboxylic acid groups of adjacent molecules.The solid-state form of the compound at room temperature is due the strong intermolecular force, such as hydrogen bonds between adjacent carboxylic acids.
It has a low solubility in water.It is not soluble in water. The hydrophobic nature of the chlorophenyl group dominates over the hydrophilic carboxylic acid group.The hydrophobic nature chlorophenyl dominates the hydrophilic carboxylic group. However, it shows better solubility in organic solvents like ethanol, methanol, and acetone.It is more soluble in organic solvents such as ethanol, methanol and acetone. These polar organic solvents can interact with both the polar carboxylic acid group through hydrogen bonding and the non - polar chlorophenyl moiety through van der Waals forces, facilitating dissolution.These polar organic solvants can interact with the polar carboxylic group through hydrogen bonds and the non-polar chlorophenyl moiety via van der Waals forces to facilitate dissolution.
Chemical Properties
The carboxylic acid functional group in 4 - Chlorophenylacrylic acid is highly reactive.The carboxylic group in 4 – Chlorophenylacrylic Acid is highly reactive. It can undergo typical acid - base reactions.It can undergo typical acid-base reactions. For example, it can react with bases such as sodium hydroxide to form the corresponding carboxylate salt.It can, for example, react with bases like sodium hydroxide to produce the carboxylate salt. This reaction is useful in various separation and purification processes.This reaction can be used in a variety of separation and purification procedures. The acidic hydrogen in the carboxylic acid group can be easily deprotonated, making 4 - Chlorophenylacrylic acid a weak acid in aqueous solutions.The carboxylic group's acidic hydrogen can be easily deprotonated to make 4 - Chlorophenylacrylic Acid a weak acid.
The double bond in the acrylic acid part of the molecule is also a site of reactivity.The double bond of the acrylic acid molecule is a reactivity site. It can participate in addition reactions.It can be involved in addition reactions. For instance, it can react with bromine in an addition reaction across the double bond, forming a dibromo derivative.It can, for example, react with bromine to form a dibromo-derivative in an addition reaction. This reaction is often used to test for the presence of carbon - carbon double bonds.This reaction is used to test for double carbon-carbon bonds.
The chlorine atom on the phenyl ring also influences the reactivity of the molecule.The chlorine atom in the phenyl rings can also influence the reactivity. The electron - withdrawing effect of the chlorine atom can affect the electron density of the phenyl ring.The electron-withdrawing effect of chlorine can affect the electron densities of the phenyl rings. This can impact the reactivity of the ring in electrophilic aromatic substitution reactions.This can affect the reactivity in electrophilic aromatic substitute reactions. Compared to unsubstituted phenyl rings, the presence of the chlorine atom can direct incoming electrophiles to specific positions on the ring, typically the ortho and para positions relative to the chlorine atom.The presence of a chlorine atom on a phenyl ring can direct electrophiles towards specific positions, usually the ortho and para positions in relation to the chlorine.
4 - Chlorophenylacrylic acid can also be involved in esterification reactions.Chlorophenylacrylic Acid can also be used in esterification reactions. When reacted with alcohols in the presence of an acid catalyst, it forms esters.When it reacts with alcohols, in the presence an acid catalyst, esters are formed. These esters may have different physical and chemical properties compared to the parent acid, and can be used in various applications such as in the synthesis of fragrances or as plasticizers.These esters can have different physical and chemistry properties than the parent acid and are used in a variety of applications, such as the synthesis or plasticizers.
How to synthesize 4-Chlorophenylacrylic acid?
4 - Chlorophenylacrylic acid can be synthesized through the following general methods.The following general methods can be used to synthesize 4 - Chlorophenylacrylic Acid.
One common approach is the Perkin reaction.Perkin reaction is a common method. In this method, 4 - chlorobenzaldehyde is reacted with acetic anhydride in the presence of a base such as sodium acetate.This method involves the reaction of 4 - chlorobenzaldehyde with acetic acid in the presence a base, such as sodium anhydride.
First, prepare the reaction mixture.Prepare the reaction mixture first. Take 4 - chlorobenzaldehyde in a suitable reaction flask.In a suitable reaction flask, place 4 - chlorobenzaldehyde. Add acetic anhydride to it.Add acetic acid to it. The amount of acetic anhydride is usually in excess relative to 4 - chlorobenzaldehyde to drive the reaction forward.To drive the reaction, acetic anhydride is usually added in excess to 4 - chlorobenzaldehyde. Then, add sodium acetate.Add sodium acetate. Sodium acetate acts as a base catalyst in this reaction.In this reaction, sodium acetate is used as a catalyst.
Heat the reaction mixture.Heat the reaction mixture. The reaction typically occurs at an elevated temperature, usually around 150 - 180 degC.The reaction usually occurs at a high temperature, typically between 150-180 degC. Under these conditions, a series of chemical reactions take place.A series of chemical reactions occur under these conditions. The acetic anhydride reacts with the base (sodium acetate) to form an acetyl anion.The acetic anion reacts with the base, sodium acetate, to form acetyl anions. This acetyl anion then attacks the carbonyl carbon of 4 - chlorobenzaldehyde.This acetyl anhydride then attacks the carbonyl atom of 4 - chlorobenzaldehyde. After a series of intermediate steps, including dehydration, 4 - chlorophenylacrylic acid is formed along with acetic acid as a by - product.After a series intermediate steps, such as dehydration, acetic acid is produced along with 4 - chlorophenylacrylic.
After the reaction is complete, cool the reaction mixture.After the reaction has completed, cool down the reaction mixture. Then, it can be treated with water.After cooling, you can treat it with water. The formed 4 - chlorophenylacrylic acid may precipitate out.The 4 - chlorophenylacrylic acids may precipitate. It can be further purified by techniques such as recrystallization.It can be purified further by techniques like recrystallization. Recrystallization is carried out by dissolving the crude product in a suitable solvent (such as ethanol or a mixture of ethanol and water) at an elevated temperature.Recrystallization involves dissolving crude product at high temperatures in a solvent (such as water or ethanol). As the solution cools, pure 4 - chlorophenylacrylic acid crystallizes out, leaving impurities in the solution.As the solution cools down, the 4 - chlorophenylacrylic acids crystallize out, leaving the impurities behind.
Another method could involve using the Knoevenagel condensation.Another method would be to use the Knoevenagel condensate. 4 - chlorobenzaldehyde can be reacted with malonic acid in the presence of a weak base like pyridine.In the presence of pyridine, 4 - chlorobenzaldehyde may be reacted to malonic acid. Malonic acid reacts with the base to form a carbanion.The carbanion is formed when malonic acid reacts to the base. This carbanion attacks the carbonyl group of 4 - chlorobenzaldehyde.This carbanion attacks 4 - chlorobenzaldehyde's carbonyl group. Subsequent decarboxylation occurs during the reaction process to yield 4 - chlorophenylacrylic acid.During the reaction, a subsequent decarboxylation takes place to produce 4 - chlorophenylacrylic acids. Similar to the Perkin reaction, after the reaction, the product can be isolated and purified.After the reaction, similar to the Perkin Reaction, the product can also be isolated and purified. The purification steps might include filtration, washing, and recrystallization to obtain high - purity 4 - chlorophenylacrylic acid.Purification steps may include filtration, washing and recrystallization in order to obtain a high-purity 4 - chlorophenylacrylic acids.
What are the safety precautions when handling 4-Chlorophenylacrylic acid?
When handling 4 - Chlorophenylacrylic acid, several safety precautions are necessary.Safety precautions must be taken when handling 4 - Chlorophenylacrylic Acid.
First, in terms of personal protective equipment.Personal protective equipment is the first thing to consider. Wear appropriate respiratory protection.Wear respiratory protection. Since 4 - Chlorophenylacrylic acid may release dust or fumes during handling, a particulate respirator with a suitable filter rating can prevent inhalation of harmful particles.A particulate respirator that has a filter rating suitable for 4 - chlorophenylacrylic can help prevent inhalation. This helps avoid potential irritation or damage to the respiratory tract, such as coughing, shortness of breath, or more serious long - term lung problems.This can help prevent respiratory irritation or damage, such as coughing or shortness of breathe, or even more serious long-term lung problems.
Eye protection is also crucial.Eye protection is equally important. Chemical - splash goggles should be worn at all times.Wear chemical splash goggles at all times. 4 - Chlorophenylacrylic acid can cause eye irritation, redness, and potentially damage the cornea if it comes into contact with the eyes.If it comes in contact with the eye, 4 - chlorophenylacrylic can cause irritation, redness and even corneal damage. Goggles create a barrier to prevent any accidental splashes from reaching the eyes.Goggles act as a barrier, preventing any accidental splashes reaching the eyes.
Gloves made of suitable materials, like nitrile gloves, are essential for hand protection.Gloves made from suitable materials like nitrile are essential for hand safety. Skin contact with 4 - Chlorophenylacrylic acid can lead to skin irritation, itching, and possible allergic reactions.Skin contact with 4 – Chlorophenylacrylic Acid can cause skin irritation, itching and allergic reactions. Gloves prevent the acid from directly touching the skin.Gloves will prevent the acid from touching your skin. Also, wear a laboratory coat or appropriate protective clothing to safeguard the body from spills and splashes.Wear a lab coat or other protective clothing to protect your body from splashes and spills.
When handling 4 - Chlorophenylacrylic acid in a laboratory or industrial setting, ensure good ventilation.In a laboratory or industrial environment, it is important to ensure that the acid is handled with good ventilation. Work in a well - ventilated area or use a fume hood.Use a fume-hood or work in an area that is well-ventilated. Adequate ventilation helps to quickly remove any fumes or dust that may be generated during handling, reducing the concentration of potentially harmful substances in the air and minimizing the risk of inhalation.Adequate ventilation is important to quickly remove any dust or fumes that may be produced during handling. This reduces the concentration of potentially dangerous substances in the air, and minimizes the risk of inhalation.
In case of spills, act promptly.Act quickly in the event of spills. First, isolate the area to prevent others from coming into contact with the spilled acid.Isolate the area first to prevent others from coming in contact with the acid. Use appropriate absorbent materials, such as sand or an inert absorbent powder, to soak up the spill.To absorb the spill, use absorbent materials such as sand, or an inert powder. Then, carefully collect the contaminated absorbent and place it in a proper waste container.Collect the contaminated absorbent carefully and place it into a suitable waste container. Clean the spill area thoroughly with a suitable cleaning agent and water to remove any remaining traces of the acid.To remove any remaining acid, clean the spill area with water and a suitable cleaning agent.
Finally, always follow proper storage procedures.Always follow the correct storage procedures. Store 4 - Chlorophenylacrylic acid in a cool, dry place away from heat sources, ignition sources, and incompatible substances.Store 4 - chlorophenylacrylic in a cool and dry place, away from heat sources, ignitions sources, and other incompatible substances. Keep it in a tightly sealed container to prevent the release of fumes and to avoid moisture absorption, which could affect its chemical properties and potentially lead to dangerous reactions.Keep it in a tightly-sealed container to prevent fumes from escaping and moisture absorption. This could affect the chemical properties of the acid and lead to dangerous reactions.
What are the storage conditions for 4-Chlorophenylacrylic acid?
4 - Chlorophenylacrylic acid should be stored under specific conditions to maintain its quality and stability.To maintain its quality, the chlorophenylacrylic Acid should be stored in a specific way.
First, it is advisable to store it in a cool place.It is best to store the 4 - Chlorophenylacrylic acid in a cool area. High temperatures can accelerate chemical reactions, potentially leading to decomposition or changes in the structure of 4 - Chlorophenylacrylic acid.High temperatures can speed up chemical reactions and cause 4 - chlorophenylacrylic acids to decompose or change in structure. A storage temperature around 2 - 8 degC is often recommended, similar to the temperature range of a common refrigerator's chilled compartment.Storage temperatures between 2 and 8 degC are often recommended. This is similar to the temperature range in a refrigerator's chilled compartment. This lower temperature slows down any possible chemical degradation processes, such as oxidation or hydrolysis reactions that might occur over time.This lower temperature slows any possible chemical degradation reactions, such as oxidation and hydrolysis reactions.
Secondly, it should be stored in a dry environment.Second, it should always be stored in a completely dry environment. Moisture can have a significant impact on the compound.Moisture has a major impact on the compound. Water can initiate hydrolysis reactions, where the chemical bonds in 4 - Chlorophenylacrylic acid are broken due to the presence of water molecules.Water molecules can cause hydrolysis reactions in which the chemical bonds of 4 - chlorophenylacrylic acids are broken. This can change the chemical properties and purity of the substance.This can alter the chemical properties and purity. To ensure a dry storage environment, desiccants can be placed in the storage container or the storage area.Desiccants are used to create a dry environment in the storage container. Silica gel is a common desiccant that can absorb moisture from the surrounding air, helping to keep the 4 - Chlorophenylacrylic acid dry.Silica gel can absorb moisture in the air and help to keep 4 - chlorophenylacrylic acids dry.
Thirdly, it is important to store 4 - Chlorophenylacrylic acid in a tightly sealed container.Thirdly, you should store the 4 - chlorophenylacrylic in a tightly closed container. This serves multiple purposes.This has multiple uses. It helps to prevent the entry of moisture and air.It prevents moisture and air from entering. Exposure to air can lead to oxidation, especially if there are reactive functional groups in the 4 - Chlorophenylacrylic acid molecule.Exposure to air may cause oxidation of the 4 - chlorophenylacrylic acids, especially if they contain reactive functional groups. A sealed container also helps to contain any potential vapors that might be released from the compound, preventing contamination of the surrounding area and protecting the integrity of the substance itself.A sealed container can also help to contain any vapors released by the compound. This prevents contamination of the area and protects the integrity of the substance. Additionally, a tightly sealed container can protect the compound from light.A tightly sealed container will also protect the compound against light. Light - induced reactions can also occur in some organic compounds, and by minimizing light exposure, the stability of 4 - Chlorophenylacrylic acid can be maintained.Some organic compounds can also be affected by light-induced reactions. By minimizing exposure to light, it is possible to maintain the stability of 4-Chlorophenylacrylic Acid. Dark - colored storage containers or storing it in a dark place can further reduce the impact of light on the compound.Storage in dark-colored containers or in a dark area can reduce the impact of the light on the compound.
In conclusion, proper storage of 4 - Chlorophenylacrylic acid involves maintaining a cool, dry environment with the compound stored in a tightly sealed container to protect it from heat, moisture, air, and light, all of which can potentially degrade the quality of this chemical.The storage of 4 – Chlorophenylacrylic Acid is best done in a cool and dry environment. The compound should be stored in a tightly-sealed container to prevent it from being damaged by heat, moisture, light, or air.