What is the chemical structure of 2-METHYL-ACRYLICACID2-OXO-TETRAHYDRO-FURAN-3-YLESTER?

1. Analysis of the name componentsAnalysis and analysis of the name components - 2 - Methyl - acrylic acid: Also known as methacrylic acid.- 2 Methyl-acrylic Acid: Also known by the name methacrylic. Its chemical formula is \(C_4H_6O_2\).Its chemical name is (C_4H_6O_2). The structure has a double - bond (\(C = C\)) and a carboxylic acid group (\(-COOH\)).The structure contains a double-bond ((C =C)) as well as a carboxylic group (\(-COOH \)). The carbon chain has four carbon atoms, with a methyl group (\(-CH_3\)) attached to the second carbon atom from the carboxylic acid end.The carbon chain contains four carbon atoms. A methyl group (\(-CH_3()) is attached to the second carbon from the carboxylic end. The structure can be written as \(CH_2 = C(CH_3)-COOH\).The structure is written as (CH_2 = C_3-COOH).
- 2 - Oxo - tetrahydro - furan - 3 - yl ester: A tetrahydro - furan ring is a five - membered ring with four carbon atoms and one oxygen atom.2 – Oxo – tetrahydro – furan – 3 – yl ester: A tetrahydro – furan ring has four carbon atoms with one oxygen atom. The prefix "2 - oxo" indicates that there is a carbonyl group (\(C = O\)) at the second position of the tetrahydro - furan ring.The prefix "2-oxo" indicates a carbonyl ((C=O)) group at the second position in the tetrahydro-furan ring. The "3 - yl" part means that the ester linkage will be formed at the third carbon atom of the tetrahydro - furan ring.The "3-yl" part indicates that the ester bond will be formed on the third carbon atom in the tetrahydro-furan ring.
2. Formation of the ester structureFormation and structure of the ester
- When 2 - Methyl - acrylic acid reacts with the alcohol equivalent derived from 2 - Oxo - tetrahydro - furan - 3 - ol (formed by considering the structure where the - OH group is at the 3 - position of the 2 - oxo - tetrahydro - furan ring) to form an ester, the reaction is a condensation reaction.The reaction occurs when 2 oxo-tetrahydro-furan ring reacts with 2 methyl-acrylic acid to form an ester. In this reaction, the - OH of the carboxylic acid (from 2 - Methyl - acrylic acid) and the - H of the alcohol group (from the 2 - Oxo - tetrahydro - furan - 3 - ol) are removed as a water molecule.In this reaction, both the OH group of the carboxylic (from 2 – Methyl-acrylic acid) and the H group of the alcohol (from the 2 Oxo – tetrahydro-furan – 3 ol) is removed as water molecules.
- The resulting chemical structure of 2 - Methyl - acrylic acid 2 - Oxo - tetrahydro - furan - 3 - yl ester has a methacrylic acid moiety (the part from 2 - Methyl - acrylic acid) and a 2 - oxo - tetrahydro - furan - 3 - yl moiety connected by an ester linkage (\(-COO-\)).The resulting chemical structure is a 2 Methyl-acrylic acid 2 Oxo-tetrahydro-furan -3 yl ester with a methacrylic moiety (the portion from 2 Methyl-acrylic acid) and 2 oxo-tetrahydro-furan -3 yl moiety linked by an ester linkage (\(-COO -\)).
- The overall chemical formula of 2 - Methyl - acrylic acid 2 - Oxo - tetrahydro - furan - 3 - yl ester can be determined by combining the molecular formulas of the two components involved in the esterification.The molecular formulas for the two components involved in esterification can be combined to determine the overall chemical formula. The molecular formula of the ester is \(C_9H_12O_4\).The molecular form of the ester (C_9H_12O_4) is given below.
- The structure has a double - bond (\(C = C\)) from the methacrylic acid part, a carbonyl group (\(C = O\)) in the ester linkage, and another carbonyl group (\(C = O\)) within the 2 - oxo - tetrahydro - furan ring.The structure contains a double-bond (C = C), a carbonyl ring (C = O), and another carbonyl ring (C = O), all from the methacrylic part. The carbon - carbon double - bond in the methacrylic acid part can participate in polymerization reactions, which may be important in various applications such as in the synthesis of polymers.The double - carbon bond in the methacrylic part can participate in polymerization, which is important in many applications such as the synthesis polymers. The 2 - oxo - tetrahydro - furan ring can also influence the physical and chemical properties of the molecule, such as solubility and reactivity, due to its cyclic structure and the presence of the carbonyl group within the ring.Due to its cyclic nature and the presence within the ring of a carbonyl group, the 2 - oxo- tetrahydro-furan ring can influence the physical and chemistry properties of the molecule.

What are the main applications of 2-METHYL-ACRYLICACID2-OXO-TETRAHYDRO-FURAN-3-YLESTER?

2 - Methyl - acrylic acid 2 - oxo - tetrahydro - furan - 3 - ylester, also known as a specific ester compound, has several main applications.The ester compound 3 - 3- ylester is also known as 2 oxo-tetrahydro-furan.
In the field of polymers, it can be used as a monomer for polymerization reactions.It can be used in polymerization reactions as a monomer. The unique structure of this ester allows it to contribute specific properties to the resulting polymers.This ester's unique structure allows it to impart specific properties to polymers. For example, when incorporated into acrylic - based polymers, it can modify the polymer's solubility, hardness, and adhesion properties.When incorporated into acrylic-based polymers, for example, it can modify its solubility, hardness and adhesion. These polymers can be used in coatings.These polymers are suitable for coatings. Coatings made with polymers containing this ester may have enhanced durability, scratch - resistance, and chemical resistance.Coatings containing polymers containing the ester may be more durable, scratch-resistant, and chemical resistant. They can be applied to various substrates such as metals, plastics, and wood, protecting them from environmental factors like moisture, oxidation, and abrasion.They can be used on a variety of substrates including metals, wood, and plastics. They protect them from environmental factors such as moisture, oxidation and abrasion.

In the production of adhesives, 2 - Methyl - acrylic acid 2 - oxo - tetrahydro - furan - 3 - ylester can play a crucial role.In the production process of adhesives, the 2 – Methyl – Acrylic acid 2 – Oxo – Tetrahydro ­ Furan — 3 ylester plays a key role. The ester can improve the adhesive's bonding strength and compatibility with different materials.The ester can increase the adhesive's compatibility and bonding strength with different materials. It helps in creating strong and long - lasting bonds between various substances.It helps to create strong and long-lasting bonds between different substances. Adhesives formulated with this compound are useful in industries like packaging, where reliable bonding of different packaging materials is essential.Adhesives made with this compound can be used in industries such as packaging, where a reliable bonding between different packaging materials is important. In the automotive industry, adhesives containing this ester can be used for bonding interior components, ensuring a secure and durable connection.Adhesives containing this ester are used in the automotive industry to bond interior components. This ensures a durable and secure connection.

This ester may also find applications in the field of drug delivery systems.This ester could also be used in the field of drug-delivery systems. Due to its specific chemical structure, it can potentially be used to modify the release rate of drugs.Its specific chemical structure can be used to alter the release rate of drugs. It can be incorporated into polymeric matrices that encapsulate drugs.It can be incorporated in polymeric matrixes that encapsulate drug. The properties of the ester - containing polymer can be tailored to control the diffusion and degradation of the matrix, thus regulating the release of the drug over time.The ester-containing polymer's properties can be tailored to control diffusion and degradation, thereby regulating the release rate of the drug. This can be beneficial for sustained - release drug formulations, improving the efficacy and convenience of drug administration.This can be advantageous for sustained-release drug formulations. It improves the efficacy of the drug and ease of administration.

Moreover, in the realm of fine chemicals synthesis, 2 - Methyl - acrylic acid 2 - oxo - tetrahydro - furan - 3 - ylester can serve as an important intermediate.In the field of fine chemicals, 2 – Methyl – acrylic acid 2– oxo– tetrahydro–furan -3 ylester is an important intermediate. It can participate in various chemical reactions, enabling the synthesis of more complex and specialized compounds.It can be used in a variety of chemical reactions to create more complex and specialized chemicals. These compounds may have applications in fragrances, flavors, or other high - value - added chemical products.These compounds can be used in the production of fragrances, flavors or other high-value-added chemical products. For instance, through further chemical modifications, it can be used to create unique molecular structures that contribute to specific olfactory or gustatory properties in the fragrance and flavor industries.Through further chemical modification, it can be utilized to create unique molecular structure that contributes to specific olfactory and gustatory properties within the fragrance and flavor industries.

What are the safety precautions when handling 2-METHYL-ACRYLICACID2-OXO-TETRAHYDRO-FURAN-3-YLESTER?

2 - Methyl - acrylic acid 2 - oxo - tetrahydro - furan - 3 - ylester is a chemical compound that requires careful handling due to potential hazards.The chemical compound 2 – Methyl-Acrylic Acid 2 – Oxo-Tetrahydro-Furan – 3 – Ylester has potential hazards and should be handled with care.
First, personal protective equipment is essential.Wearing appropriate chemical-resistant gloves is essential. Wear appropriate chemical - resistant gloves, preferably made of materials like nitrile or neoprene.Wear gloves that are resistant to chemicals, preferably made from nitrile or Neoprene. These gloves protect your hands from direct contact with the chemical, which could cause skin irritation, burns, or absorption into the body.These gloves protect you from the chemicals that could cause skin irritations, burns or absorption in the body. Also, use safety goggles or a face shield to safeguard your eyes.Use safety goggles, or a face mask to protect your eyes. Splashes of the compound can lead to serious eye damage, including corneal abrasions or even loss of vision.Splashes of this compound can cause serious eye damage including corneal abrasions and even loss of sight.

When handling this substance, ensure good ventilation.When handling this substance ensure that you have good ventilation. Work in a well - ventilated area, such as a fume hood if available.If possible, work in an area that is well-ventilated. Inadequate ventilation can allow the vapors of the compound to accumulate in the air.Inadequate ventilation may allow the compound vapors to accumulate in the atmosphere. Inhaling these vapors may cause respiratory problems, like irritation of the nose, throat, and lungs.Inhaling the vapors can cause respiratory problems such as irritation of the nose and throat. Prolonged or high - concentration exposure could potentially lead to more severe respiratory disorders.Exposure to high concentrations or for a long time could lead to respiratory problems.

Storage is another important aspect.Storage is also important. Store 2 - Methyl - acrylic acid 2 - oxo - tetrahydro - furan - 3 - ylester in a cool, dry place away from heat sources and ignition sources.Store 2 – Methyl-acrylic acid 2 – Oxo-tetrahydro-furan – 3 – ylester away from heat and ignition sources in a cool and dry place. It is often flammable, and heat or an open flame can initiate a fire.Heat or an open flame may cause a fire. Keep it in a properly labeled container to avoid confusion and ensure that it is stored separately from incompatible substances.Store it in a container that is clearly labeled to avoid confusion. Also, store it away from other substances. Some chemicals can react violently with it, resulting in fires, explosions, or the release of toxic gases.Some chemicals can react violently, resulting in explosions, fires or toxic gas releases.

In case of a spill, act quickly and carefully.Act quickly and carefully in the event of a spill. First, evacuate the area if the spill is large or if there is a risk of vapor inhalation.If the spill is large, or there is a danger of vapor inhalation, you should evacuate the area. Then, wear appropriate protective gear and use absorbent materials, like vermiculite or sand, to soak up the spill.Wear protective gear, and then use absorbent materials like vermiculite, or sand to soak up spills. Dispose of the contaminated absorbent in accordance with local environmental regulations.Dispose of contaminated absorbent according to local environmental regulations. Do not wash the spill into the drains as it may contaminate water sources.Do not flush the spill down the drains, as it could contaminate the water source.

If you come into contact with the compound, take immediate action.Take immediate action if you come into contact. For skin contact, remove contaminated clothing and wash the affected area thoroughly with soap and water for at least 15 minutes.If skin contact occurs, remove the contaminated clothing and thoroughly wash the affected area with soap and warm water for 15 minutes. Seek medical attention if irritation persists. In case of eye contact, flush the eyes with copious amounts of water for at least 15 minutes, lifting the eyelids occasionally to ensure complete rinsing, and then get medical help promptly.If you have eye contact, rinse your eyes for at least 15 mins with plenty of water, lifting the eyelids to ensure that the entire eye is rinsing. Then, seek medical attention immediately. If inhaled, move to fresh air immediately.If inhaled, get to fresh air as soon as possible. If breathing is difficult, provide artificial respiration if trained to do so and call for emergency medical services.If breathing is difficult, if you are trained to do so, use artificial respiration and call emergency medical services.

What is the solubility of 2-METHYL-ACRYLICACID2-OXO-TETRAHYDRO-FURAN-3-YLESTER in different solvents?

The solubility of 2 - METHYL - ACRYLIC ACID 2 - OX0 - TETRAHYDRO - FURAN - 3 - YLESTER in different solvents can vary significantly based on the nature of the solvent and the solute.The solubility in different solvents of 2 METHYL ACRYLIC ACID, OX0 TETRAHYDRO FURAN -3 YLESTER can vary greatly depending on the nature of both the solvent and solute.
In polar solvents like water, the solubility is likely to be relatively low.In polar solvents such as water, solubility will be low. This is because the 2 - METHYL - ACRYLIC ACID 2 - OX0 - TETRAHYDRO - FURAN - 3 - YLESTER molecule has a non - polar backbone with a relatively small polar functional group.This is due to the fact that the 2 METHYL – ACRYLIC ACID – OX0 – TETRAHYDRO – FURAN 3 YLESTER molecule contains a non polar backbone and a small polar functional group. Water is a highly polar solvent, and the non - polar parts of the solute will have a tendency to aggregate rather than disperse among the water molecules due to hydrophobic interactions.Water is a highly-polar solvent. The non-polar parts of a solute will tend to aggregate, rather than disperse, among the water molecules because of hydrophobic interactions.

Alcohols, on the other hand, can show different solubility behaviors.Alcohols can have different solubility characteristics. Lower - molecular - weight alcohols such as methanol and ethanol are polar solvents, but they also have non - polar methyl or ethyl groups.Alcohols with lower molecular weights, such as methanol or ethanol, are polar solvents. However, they also contain non-polar methyl and ethyl group. The polar - OH group can form hydrogen bonds with the polar functional groups in the 2 - METHYL - ACRYLIC ACID 2 - OX0 - TETRAHYDRO - FURAN - 3 - YLESTER, while the non - polar part of the alcohol can interact with the non - polar regions of the solute through van der Waals forces.The polar OH group can form hydrogen bond with the polar functional group in the 2 METHYL – ACRYLIC ACID, 2 – OX0 – TETRAHYDRO – FURAN 3 YLESTER. Meanwhile, the non polar alcohol can interact with non polar regions of a solute using van der Waals forces. So, the solubility in methanol and ethanol is likely to be higher than in water.Solubility is higher in methanol or ethanol than in water. As the carbon chain length of the alcohol increases, the non - polar character of the alcohol becomes more dominant, and the solubility may further increase.As the length of the carbon chain increases, the non-polar character of alcohol becomes more dominant and solubility can increase. For example, in butanol, the longer non - polar chain can better accommodate the non - polar parts of the solute, potentially leading to enhanced solubility compared to methanol.In butanol for example, the longer non-polar chain can accommodate the non-polar parts of the solution, potentially leading to increased solubility when compared to methanol.

In non - polar solvents like hexane or toluene, the solubility is expected to be high.The solubility of hexane and toluene is expected to high. The non - polar nature of these solvents allows for favorable interactions with the non - polar regions of the 2 - METHYL - ACRYLIC ACID 2 - OX0 - TETRAHYDRO - FURAN - 3 - YLESTER molecule.The non polar nature of the solvents allows for favorable interaction with the non polar regions of 2 METHYL – ACRYLIC ACID – OX0 – TETRAHYDRO – FURAN 3 YLESTER molecule. The van der Waals forces between the non - polar solvent molecules and the non - polar parts of the solute enable the solute to dissolve readily.The Van der Waals forces that exist between the non-polar solvent molecules, and the non-polar parts of the solution, allow the solute to dissolve easily. Toluene, with its aromatic ring, can also interact with the solute through pi - pi stacking interactions if the solute has suitable pi - electron - rich regions, further promoting solubility.Toluene's aromatic ring can also interact with a solute via pi - pi stacking if the solute contains suitable pi – electron-rich regions. This will further promote solubility.

Halogenated solvents such as dichloromethane also have intermediate polarity.Halogenated solvents, such as dichloromethane, also have intermediate polarity. The partial charges on the chlorine atoms in dichloromethane can interact with the polar functional groups of the solute, while the overall non - polar nature of the molecule can accommodate the non - polar parts.The partial charges of the chlorine atoms can interact with polar functional groups in the solute while the overall non-polar nature of a molecule can accommodate non-polar parts. So, the solubility in dichloromethane is likely to be significant, providing a good balance for dissolving the 2 - METHYL - ACRYLIC ACID 2 - OX0 - TETRAHYDRO - FURAN - 3 - YLESTER.Solubility of dichloromethane will be high, providing a good equilibrium for dissolving 2 - METHYL – ACRYLIC ACID, 2 – OX0 – TETRAHYDRO-FURAN, 3 – YLESTER.

In summary, the solubility of 2 - METHYL - ACRYLIC ACID 2 - OX0 - TETRAHYDRO - FURAN - 3 - YLESTER is low in highly polar solvents like water, higher in polar - non - polar hybrid solvents such as alcohols, and relatively high in non - polar solvents like hexane, toluene, and in intermediate - polarity halogenated solvents like dichloromethane.The solubility of 2-METHYL-ACRYLIC ACID is low in highly-polar solvents, such as water. It is higher in polar-non-polar hybrid solvents, like alcohols. It is relatively high in non-polar solvents, like hexane and toluene.

What is the purity of 2-METHYL-ACRYLICACID2-OXO-TETRAHYDRO-FURAN-3-YLESTER typically available in the market?

The purity of 2 - METHYL - ACRYLICACID2 - OXOTETRAHYDRO - FURAN - 3 - YLESTER available in the market can vary significantly depending on several factors.The purity of the 2 - METHYL – ACRYLICACID2 OXOTETRAHYDRO- FURAN 3 – YLESTER on the market can be affected by several factors.
Firstly, the production method plays a crucial role.First, the production method is crucial. Different manufacturing processes can yield products with different levels of purity.Different manufacturing processes can produce products with varying levels of purity. For instance, if a more refined and precise synthetic route is employed, it is more likely to result in a higher - purity product.If a more refined and accurate synthetic route is used, it will likely result in a product with a higher purity. High - end manufacturing facilities with advanced purification techniques such as distillation, chromatography, or recrystallization are better equipped to produce 2 - METHYL - ACRYLICACID2 - OXOTETRAHYDRO - FURAN - 3 - YLESTER with high purity.High-end manufacturing facilities equipped with advanced purification methods such as distillation or chromatography are better able to produce 2 METHYL ACRYLICACID2 OXOTETRAHYDRO-FURAN -3 YLESTER.

Secondly, the intended use of the compound also affects the typical purity levels.Second, the intended purpose of the compound will also influence the typical purity level. If it is for research purposes, especially in applications where high - precision and accurate results are required, such as in pharmaceutical research or certain chemical analysis, the purity might be expected to be very high.Purity levels can be high for research, and especially in applications that require high precision and accuracy, such as pharmaceutical research or certain chemical analyses. In these cases, suppliers often strive to offer products with purity levels upwards of 95% or even 98 - 99%.In these cases suppliers strive to offer products that have purity levels of up to 95%, or even 98-99%. This high purity ensures that the experimental results are not skewed by the presence of impurities.This high purity ensures the results of experiments are not distorted by the presence impurities.

On the other hand, if the 2 - METHYL - ACRYLICACID2 - OXOTETRAHYDRO - FURAN - 3 - YLESTER is intended for more general industrial applications like in some polymerization processes where a small amount of impurities might not have a major impact on the overall process outcome, the purity could be lower.Purity could be lower if the 2 -- METHYL-ACRYLICACID2 -- OXOTETRAHYDRO-FURAN- 3- YLESTER was intended for general industrial applications, such as in polymerization processes, where a small amount impurities may not have a significant impact on the process outcome. In such scenarios, products with purity levels around 80 - 90% might be commonly available.In such scenarios, it is possible to find products with a purity level of 80 - 90 %.

Moreover, the cost - effectiveness also influences the purity.The cost-effectiveness also affects the purity. Higher - purity products usually come at a higher cost due to the additional purification steps involved.Due to the additional purification processes, higher-purity products are usually more expensive. So, in markets where cost is a major consideration, lower - purity options might be more prevalent.In markets where cost is an important factor, lower-purity options may be more common.

In general, while it is difficult to pinpoint a single typical purity value, in the high - end research - grade market, purity levels of around 95 - 99% are common.While it is difficult to pinpoint one typical purity value, on the high-end research-grade market, levels of purity between 95-99% are quite common. In the industrial - grade market, purity can range from 80 - 90%.In the industrial-grade market, purity levels can range between 80-90 percent. However, these are just general estimates, and the actual purity can vary from one supplier to another and also depending on market demands and trends at a given time.These are only general estimates. The actual purity may vary from one supplier or market to another, as well as depending on the current trends and market demands.