What is the application of 3-Furanylacrylic acid?

3 - Furanylacrylic acid has several important applications.Furanylacrylic Acid has many important applications.
In the field of pharmaceuticals, it serves as a valuable intermediate.It is a valuable intermediary in the pharmaceutical industry. It can be used in the synthesis of various drugs.It can be used to synthesize various drugs. For example, some compounds derived from 3 - furanylacrylic acid may possess anti - inflammatory properties.Some compounds derived 3 -furanylacrylic acids may have anti-inflammatory properties. Scientists can modify its chemical structure to create new molecules that can interact with specific biological targets in the body, such as receptors involved in the inflammatory response pathway.Scientists can alter its chemical structure to produce new molecules that interact with specific biological targets, such as receptors in the inflammatory response pathway. This can potentially lead to the development of more effective anti - inflammatory medications with fewer side effects compared to existing drugs.This could lead to the creation of anti-inflammatory drugs with fewer side effects than existing drugs.

In the fragrance industry, 3 - furanylacrylic acid plays a significant role.In the fragrance industry 3 -furanylacrylic acids plays a major role. It has a pleasant and unique aroma.It has a pleasant, unique aroma. It can be used either on its own or as a key ingredient in formulating complex perfume compositions.It can be used as a standalone ingredient or as an important component in complex perfume compositions. The compound's distinct smell can add a special note to perfumes, giving them a more refined and appealing scent.The distinct smell of the compound can give perfumes a refined and appealing scent. Its presence can enhance the overall olfactory experience of a fragrance, making it stand out in a crowded market of perfume products.Its presence can enhance a fragrance's overall olfactory appeal, making it standout in a crowded perfume market.

In the area of food additives, 3 - furanylacrylic acid has applications as well.The 3 -furanylacrylic acids has also applications in the field of food additives. It can be used as a flavor enhancer.It can be used to enhance flavor. The compound can impart a certain flavor profile to food products.The compound can be used to impart a specific flavor profile to food. For instance, in the production of baked goods, it can add a warm, nutty, and slightly sweet flavor.In the production of baked goods it can add a warm nutty and slightly sweet taste. In the beverage industry, it can be used to enhance the flavor of certain types of drinks, making them more palatable and attractive to consumers.It can be used in the beverage industry to enhance the taste of certain drinks, making them more appealing to consumers. It is often used in small amounts to achieve the desired flavor modification without overwhelming the natural taste of the food or beverage.It is used in small quantities to achieve the desired taste modification without overwhelming the natural flavor of the food or drink.

In addition, 3 - furanylacrylic acid is also used in some research studies related to organic chemistry and material science.In addition, 3 – furanylacrylic acids is also used for research studies in organic chemistry and materials science. In organic synthesis research, it can be used to explore new reaction pathways and create novel organic compounds.In organic synthesis, it can be used in research to explore new reactions pathways and create novel compounds. In material science, it may be involved in the development of certain polymers or materials with specific properties.In material science, the development of polymers or materials that have specific properties may involve it. For example, it could potentially be incorporated into polymers to improve their solubility, stability, or other physical and chemical characteristics, which can be useful in applications such as coatings or packaging materials.It could be incorporated into polymers in order to improve their solubility or stability or other physical and chemistry characteristics. This can be useful for applications such as coatings and packaging materials.

What are the properties of 3-Furanylacrylic acid?

3 - Furanylacrylic acid is an organic compound with several notable properties.Furanylacrylic Acid is a compound with many notable properties.
Physical properties:Physical Properties
In terms of appearance, 3 - Furanylacrylic acid is typically a solid.3 - Furanylacrylic Acid is usually a solid. It often exists as yellow - white or light - colored crystals.It is often found as yellow-white or light-colored crystals. The melting point of 3 - furanylacrylic acid is around 138 - 141 degC.The melting point for 3 - Furanylacrylic Acid is between 138 and 141 degrees Celsius. This relatively high melting point is due to the presence of strong intermolecular forces within the crystal lattice.This high melting point is a result of the strong intermolecular forces in the crystal lattice. The compound has a characteristic odor, which can be described as somewhat sweet and floral, and this property makes it useful in the perfume industry.This compound has a distinctive odor that can be described as floral and sweet. This property makes it useful for the perfume industry.

Solubility: 3 - Furanylacrylic acid shows limited solubility in water.Solubility: Furanylacrylic Acid is only soluble in water to a limited extent. It is sparingly soluble in polar solvents like water because its structure contains a relatively non - polar furan ring and an acrylic acid moiety.It is only sparingly soluble because of its structure, which contains a non-polar furan ring with an acrylic acid moiety. However, it has better solubility in organic solvents such as ethanol, methanol, and acetone.It is more soluble in organic solvents like acetone, ethanol, and methanol. These organic solvents can interact with the non - polar parts of the molecule through van der Waals forces and also with the carboxylic acid group through hydrogen bonding, facilitating dissolution.These organic solvents interact with the non-polar parts of the molecules through van der Waals force and also with carboxylic acid groups through hydrogen bonding to facilitate dissolution.

Chemical properties:Chemical properties
The carboxylic acid group in 3 - furanylacrylic acid is highly reactive.The carboxylic group in 3 – furanylacrylic acids is highly reactive. It can participate in acid - base reactions.It can be involved in acid-base reactions. For example, it can react with bases such as sodium hydroxide to form the corresponding carboxylate salt and water.It can, for example, react with bases like sodium hydroxide in order to form the carboxylate salts and water. This reaction is a typical characteristic of carboxylic acids.This reaction is characteristic of carboxylic acid. The double bond in the acrylic acid part of the molecule is also reactive.The double bond of the acrylic acid molecule is also reactive. It can undergo addition reactions.It can undergo addition reaction. For instance, it can react with bromine in an addition reaction to add bromine atoms across the double bond, forming a dibromo - derivative.It can, for example, react with bromine to add bromine across the double bond in an addition reaction, forming a derivative called dibromo. This double - bond reactivity also allows 3 - furanylacrylic acid to participate in polymerization reactions.This double-bond reactivity allows 3 – furanylacrylic acids to participate in polymerization. Under appropriate conditions, the double bond can be induced to break and form long - chain polymers, which can have various applications in materials science.Under the right conditions, it is possible to induce the double bond to break, forming long-chain polymers that can be used in various materials science applications.
The furan ring in the molecule also has its own reactivity.Furan ring also has its own reactivity. Although furan is an aromatic compound, it is less aromatic than benzene.Furan is an aromatic compound but it is less aromatic than the benzene. The electrons in the furan ring can participate in electrophilic aromatic substitution reactions.The electrons of the furan ring are involved in electrophilic aromatic substitute reactions. For example, it can react with electrophiles such as nitronium ions (in nitration reactions) or acylating agents (in Friedel - Crafts acylation reactions), where the electrophile substitutes a hydrogen atom on the furan ring.It can, for example, react with electrophiles like nitronium (in nitration reaction) or acylating agent (in Friedel-Crafts acylation reaction), where the electron substitutes a hydrogen atom on furan ring. This reactivity of the furan ring, combined with the reactivity of the carboxylic acid and double - bond groups, gives 3 - furanylacrylic acid a rich chemistry for the synthesis of various derivatives.This reactivity, in combination with the reactivity and carboxylic acid groups, gives 3-furanylacrylic an extremely rich chemistry that allows for the synthesis a variety of derivatives.

How is 3-Furanylacrylic acid synthesized?

3 - Furanylacrylic acid can be synthesized through the following common methods:Furanylacrylic Acid can be synthesized using the following common methods.
1. Knoevenagel Condensation Method
This is a widely used approach.This is a widely-used approach. The starting materials are furfural and malonic acid.Furfural and malonic acids are the starting materials. In the presence of a base catalyst, such as pyridine or piperidine, the reaction occurs.The reaction occurs in the presence of a catalyst such as pyridine, piperidine or pyridine.
Furfural contains an aldehyde group.Furfural is composed of an aldehyde. Malonic acid has two carboxylic acid groups.Malonic acid contains two carboxylic acids. The base catalyst first deprotonates the acidic hydrogen of malonic acid, generating a carbanion.The base catalyst deprotonates first the acidic hydrogen in malonic acid to produce a carbanion. This carbanion then attacks the carbonyl carbon of furfural.This carbanion attacks the carbonyl of furfural. Subsequently, a series of proton - transfer and elimination reactions take place.Then, a series proton-transfer and elimination reactions occur. The elimination of carbon dioxide from the intermediate leads to the formation of 3 - furanylacrylic acid.The elimination of carbon from the intermediate results in the formation of 3-furanylacrylic Acid.
The reaction conditions are relatively mild.The reaction conditions are mild. Usually, the reaction is carried out in a solvent like pyridine or ethanol at a moderate temperature, around 80 - 120 degC.The reaction is usually carried out at a moderate temperature (80-120 degC) in a solvent such as pyridine or alcohol. After the reaction is completed, the product can be isolated through techniques such as filtration, extraction, and recrystallization.After the reaction has been completed, the product may be isolated using techniques such as filtration or extraction. For example, the reaction mixture can be cooled, and the precipitated product is filtered.The reaction mixture can, for example, be cooled and the precipitated product filtered. Then, it can be purified by recrystallizing from an appropriate solvent, like ethanol - water mixture, to obtain pure 3 - furanylacrylic acid.It can then be purified using a suitable solvent, such as ethanol-water mixture, by recrystallizing.

2. Perkin Reaction - like Process
In this method, furfural is reacted with acetic anhydride.This method involves the reaction of furfural with acetic acid. Similar to the Perkin reaction, a base such as sodium acetate is used as a catalyst.As with the Perkin reaction a base, such as sodium acetate, is used as a catalyser.
The sodium acetate deprotonates acetic anhydride to form an acetyl anion.The sodium acetate deprotonates the acetic anhydride into an acetyl anion. This anion attacks the aldehyde group of furfural.This anion attacks furfural's aldehyde groups. After a series of intramolecular rearrangements and elimination reactions, 3 - furanylacrylic acid is formed.After a series intramolecular rearrangements, and elimination reactions are formed, 3 -furanylacrylic is formed. Here, the acetate group from acetic anhydride is involved in the reaction mechanism to build the carbon - carbon double bond and the carboxylic acid functionality.The acetate group of acetic anhydride plays a role in the reaction to build the double carbon-carbon bond and carboxylic acid functionality. The reaction is typically carried out at an elevated temperature, around 150 - 200 degC, as the reactivity of acetic anhydride is relatively lower compared to malonic acid in the Knoevenagel reaction.The reaction is usually carried out at a higher temperature, between 150 and 200 degC. This is because the reactivity is lower for acetic anhydride than malonic acid. After the reaction, the product mixture may need to be treated with an acid to neutralize the base catalyst and then separated and purified.After the reaction the product mixture will need to be neutralized with an acid and then separated and purified. This can involve extraction with an organic solvent to remove unreacted starting materials and by - products, followed by distillation or recrystallization to obtain pure 3 - furanylacrylic acid.This can be done by extracting the unreacted materials and by-products with an organic solvent, followed by distillation of recrystallization or recrystallization.

What are the safety precautions when handling 3-Furanylacrylic acid?

When handling 3 - Furanylacrylic acid, several safety precautions should be observed.When handling 3 – Furanylacrylic Acid, it is important to observe several safety precautions.
First, in terms of personal protective equipment.Personal protective equipment is the first thing to consider. Wear appropriate respiratory protection.Wear respiratory protection. If there is a risk of dust or vapor exposure, a respirator with an appropriate filter should be used.Use a respirator equipped with a filter if there is a chance of exposure to dust or vapor. This helps prevent inhalation of the substance, which could potentially irritate the respiratory tract.This prevents inhalation, which can potentially irritate respiratory tracts. For the eyes, safety goggles are essential.Safety goggles for the eyes are essential. 3 - Furanylacrylic acid may cause eye irritation, and goggles provide a physical barrier to prevent any splashes or dust from coming into contact with the eyes.Goggles are a barrier that prevents dust or splashes from getting into the eyes. Furanylacrylic Acid can cause eye irritation. Gloves made of a suitable material, such as nitrile gloves, should be worn on the hands.Hands should be covered with gloves made of a suitable, non-irritating material such as nitrile. This protects the skin from direct contact, as skin contact can lead to irritation, redness, and possible allergic reactions.This will protect the skin from direct exposure, which can cause irritation, redness and allergic reactions.

Secondly, pay attention to the handling environment.Pay attention to the environment in which you are handling the product. Work in a well - ventilated area.Work in an area that is well-ventilated. Adequate ventilation helps to disperse any fumes or dust that may be generated during the handling process.Adequate ventilation is important to disperse any dust or fumes that may be produced during the handling process. If possible, use a fume hood.Use a fume-hood if possible. A fume hood can effectively capture and exhaust harmful vapors or dust, keeping the air in the working area clean and reducing the risk of inhalation exposure.A fume hood will effectively capture and exhaust harmful dust or vapors, keeping the air clean in the work area and reducing the risk for inhalation. Avoid creating dust during handling. When weighing or transferring the substance, do it gently to prevent the formation of dust particles that can be easily inhaled.Avoid creating dust when handling the substance.

Thirdly, in case of accidental contact.Thirdly, in the event of accidental contact. If 3 - Furanylacrylic acid comes into contact with the skin, immediately rinse the affected area with plenty of water for at least 15 minutes.If 3 - Furanylacrylic Acid comes into contact with your skin, immediately rinse it with plenty of water. Remove any contaminated clothing during this process.During this process, remove any contaminated clothing. If the irritation persists, seek medical attention.If irritation persists, consult a doctor. In case of eye contact, flush the eyes with copious amounts of water for at least 15 minutes, holding the eyelids open to ensure thorough rinsing.If you have had eye contact, rinse your eyes for at least 15 mins with lots of water, while keeping the eyelids wide open to ensure thorough rinsing. Then, seek immediate medical help.Seek immediate medical attention. If inhaled, move to fresh air immediately.If inhaled, get to fresh air as soon as possible. If the person is experiencing difficulty breathing, provide artificial respiration if trained to do so and call for emergency medical assistance.If the person has difficulty breathing, if you are trained to do this, you can provide artificial respiration and call emergency medical assistance.

Finally, storage is also important.Storage is also very important. Store 3 - Furanylacrylic acid in a cool, dry place away from sources of heat and ignition.Store 3 - Furanylacrylic Acid in a cool and dry place, away from heat sources and ignition. Keep it in a tightly closed container to prevent the release of vapors or the entry of moisture, which could potentially affect its chemical properties.Keep it in a tightly sealed container to prevent the release or entry of moisture that could potentially affect the chemical properties. Label the container clearly with the name of the substance and any relevant hazard warnings to ensure that others handling the storage area are aware of the potential risks.Label the container with the name of substance and any relevant warnings so that anyone handling the storage area is aware of potential risks.

What are the storage requirements for 3-Furanylacrylic acid?

3 - Furanylacrylic acid is an organic compound with specific storage requirements to maintain its quality and stability.Furanylacrylic Acid is an organic compound that requires specific storage conditions to maintain its quality.
Firstly, it should be stored in a cool environment.First, it should be kept in a cool place. High temperatures can accelerate chemical reactions, such as decomposition or polymerization.High temperatures can speed up chemical reactions such as polymerization or decomposition. A storage temperature around 2 - 8 degC is often ideal.Ideal storage temperatures are usually between 2 and 8 degC. This temperature range helps to slow down any potential thermal - induced degradation processes.This temperature range can help to slow down any thermal - induced degrading processes. For example, if stored at elevated temperatures, the double - bonds in the furan and acrylic acid moieties might react, leading to the formation of by - products and a change in the compound's chemical properties.If stored at high temperatures, double - bonds between the furan and the acrylic acid molecules may react, resulting in the formation of by-products and a change to the chemical properties of the compound.

Secondly, it needs to be stored in a dry place.Second, it must be stored in a place that is dry. Moisture can have a detrimental effect on 3 - furanylacrylic acid.Moisture may have a negative effect on 3-furanylacrylic acids. Water can initiate hydrolysis reactions, especially with the carboxylic acid group present in the molecule.Water can initiate hydrolysis, especially when the carboxylic group is present in the molecule. Hydrolysis can break the chemical structure, altering the functionality of the compound.Hydrolysis can alter the functionality of a compound by breaking the chemical structure. Additionally, moisture can promote the growth of microorganisms if the storage conditions are not properly controlled, which could also contaminate the 3 - furanylacrylic acid sample.Moisture can also promote the growth and contamination of 3 - Furanylacrylic Acid if storage conditions are not controlled properly.

Thirdly, storage should be in a well - sealed container.Thirdly, the container should be well-sealed. This is to prevent exposure to air.This will prevent the exposure to air. Oxygen in the air can cause oxidation reactions.Oxygen in air can cause oxidation. The double - bonds in the 3 - furanylacrylic acid are susceptible to oxidation, which can lead to the formation of peroxides or other oxidized products.The double-bonds in the 3-furanylacrylic acids are susceptible to oxidation. This can lead to peroxides and other oxidized products. These oxidized species can not only change the chemical nature of the 3 - furanylacrylic acid but may also pose safety risks in some cases.These oxidized species not only alter the chemical nature of 3 -furanylacrylic acids but can also pose safety risk in some cases.

Fourthly, the storage location should be away from sources of light.The storage location should be far from light sources. Ultraviolet and visible light can initiate photochemical reactions.Photochemical reactions can be initiated by ultraviolet and visible light. Photons from light can provide the energy needed to break chemical bonds in 3 - furanylacrylic acid, leading to degradation.Photons can provide the energy required to break chemical bonds, leading to degradation. For instance, light - induced isomerization or bond - cleavage reactions could occur, changing the structure and properties of the compound.Light-induced isomerizations or bond-cleavage reactions, for example, could occur and change the structure and properties.

Finally, when storing 500 grams or a similar quantity, ensure that the container is appropriate for the volume.When storing 500 g or similar quantities, make sure that the container is suitable for the volume. It should be made of a material that is chemically inert towards 3 - furanylacrylic acid, such as certain types of glass or high - density polyethylene.It should be made from a material which is chemically inert to 3 -furanylacrylic acids, such as high-density polyethylene or certain types of glass. This helps to prevent any leaching of impurities from the container into the compound and vice versa, ensuring the long - term stability of the 3 - furanylacrylic acid during storage.This will prevent the leaching of impurities into the compound from the container and vice versa. It will also ensure the long-term stability of 3 - Furanylacrylic Acid during storage.