What are the applications of 2-CYANO-3-(1-NAPHTHYL)ACRYLIC ACID + METHYL ESTER?

2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER, often referred to as a specific organic compound, has several applications.The compound 2 - CYANO -3 - (1 – NAPHTHYL )ACRYLIC ACID+ METHYL ESTER, also known as a specific chemical, has many applications.
In the field of organic synthesis, it serves as a valuable building block.It is a valuable building-block in the field of organic syntheses. Its unique structure allows chemists to create more complex organic molecules.Its unique structure allows for chemists create more complex organic molecule. For example, through various chemical reactions like condensation reactions, it can be incorporated into larger frameworks.It can be incorporated, for example, into larger frameworks through various chemical reactions such as condensation reactions. These new molecules might possess enhanced properties, such as different solubility characteristics or increased stability, which are crucial for the development of new drugs or materials.These new molecules may have enhanced properties such as different solubility or increased stability which are critical for the development of drugs or materials.

In the pharmaceutical industry, this compound could potentially be used in the synthesis of novel drugs.This compound can be used to synthesize new drugs in the pharmaceutical industry. The naphthyl group and the cyano - acrylic acid methyl ester moiety might confer specific biological activities.The naphthyl moiety and the cyano-acrylic acid methyl ester moiety may confer specific biological activity. For instance, they could interact with certain receptors in the human body.They could, for example, interact with certain receptors within the human body. Scientists can modify the structure around this core compound to optimize its binding affinity to target receptors, potentially leading to the development of drugs for treating diseases like cancer or neurological disorders.Scientists can alter the structure of this core compound in order to optimize its affinity for binding to target receptors. This could lead to the development drugs to treat diseases such as cancer or neurological disorders.

In materials science, 2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER can contribute to the creation of new polymers.In materials science, the combination of 2 - CYANO -3 - (1 – NAPHTHYL )ACRYLIC ACID and METHYL ESTER can be used to create new polymers. When polymerized, these materials may exhibit interesting optical or mechanical properties.These materials can exhibit interesting optical and mechanical properties when polymerized. They could be used in the production of optical films, where their unique molecular structure might influence light transmission and absorption.They could be used to produce optical films where their unique molecular structures might influence light absorption and transmission. This could be beneficial for applications in displays, such as LCD or OLED screens, to improve image quality and energy efficiency.This could be used to improve the image quality and energy efficiency of displays such as LCD screens or OLED screens.

Furthermore, in the area of fluorescence research, this compound might be functionalized to become a fluorescent probe.This compound could also be functionalized in the field of fluorescence to become a fluorescent probe. The presence of the naphthyl group can potentially enhance fluorescence properties.The presence of a naphthyl can potentially enhance the fluorescence properties. By attaching specific groups to the molecule, it can be made to target particular biological or chemical species.Attaching specific groups to a molecule can make it target a particular biological or chemical specie. In biological imaging, for example, it could be used to label and track specific cells or molecules within a living organism, providing valuable insights into biological processes at the cellular level.In biological imaging, it can be used to track and label specific cells or molecules in a living organism. This provides valuable insights into biological processes on the cellular level.

In conclusion, 2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER has diverse applications spanning from organic synthesis to pharmaceutical, materials, and fluorescence - related fields, highlighting its importance in modern chemical research and technological development.The 2 - CYANO -3 - (1 – NAPHTHYL )ACRYLIC ACID METHYL ESTER has a wide range of applications, ranging from organic synthesis, to pharmaceuticals, materials and fluorescence-related fields. This highlights its importance in modern chemical and technological research.

What are the properties of 2-CYANO-3-(1-NAPHTHYL)ACRYLIC ACID + METHYL ESTER?

2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER, also known as a type of naphthyl - containing cyanoacrylate derivative, has several notable properties.The 2 - CYANO -3 - (1 – NAPHTHYL )ACRYLIC ACID+ METHYL ESTER, also known a type naphthyl containing cyanoacrylate, has a number of notable properties.
Physical Properties

In terms of appearance, it is likely to be a solid at room temperature.It is likely that it will appear as a solid when at room temperature. Many organic esters with similar structures tend to exist as crystalline solids due to the relatively strong intermolecular forces.Due to the relatively strong forces between molecules, many organic esters have similar structures and tend to exist as solids. The presence of the naphthyl group, which is a large and planar aromatic moiety, contributes to the molecule's ability to stack in a regular pattern, promoting solid - state formation.The naphthyl moiety, which is a large, planar aromatic group, helps the molecule to stack in a regular manner, promoting the solid-state formation.

The compound has a characteristic melting point.The compound has its own melting point. The melting point is influenced by the strength of the intermolecular forces.The strength of intermolecular forces influences the melting point. The cyano group (- CN) and the ester group (- COOCH3) can participate in dipole - dipole interactions, while the naphthyl ring can contribute to van der Waals forces.The cyano (-CN) and ester groups (-COOCH3) can be involved in dipole-dipole interactions while the naphthyl rings can contribute to van der Waals force. These combined forces determine the temperature at which the solid - to - liquid phase transition occurs.These combined forces determine at what temperature the solid-to-liquid phase transition occurs.

Chemical Properties

The cyano group is highly reactive.The cyano group has a high level of reactivity. It can undergo addition reactions, for example, nucleophilic addition.It can undergo addition reaction, such as nucleophilic. Nucleophiles such as amines or alcohols can attack the carbon atom of the cyano group, leading to the formation of new compounds.Nucleophiles, such as alcohols or amines, can attack the carbon of the cyanogroup and lead to the formation new compounds. This reactivity is due to the polarization of the CN bond, with the carbon atom being electrophilic.This reactivity occurs due to the polarization in the CN bond. The carbon atom is electrophilic.

The double bond in the acrylic acid part of the molecule is also reactive.The double bond in acrylic acid is also reactive. It can participate in electrophilic addition reactions.It can be involved in electrophilic reactions. For instance, addition of halogens like bromine can occur across the double bond, resulting in the formation of a dibromo - derivative.Addition of halogens such as bromine can take place across the double bonds, resulting in a dibromo-derivative. This double bond can also be used in polymerization reactions under appropriate conditions.Under the right conditions, this double bond can be used to initiate polymerization reactions. Radical polymerization could potentially lead to the formation of polymers containing the naphthyl and cyano groups along the polymer chain.Radical polymerization can lead to polymers that contain naphthyl or cyano groups in the polymer chain.

The ester group (- COOCH3) is subject to hydrolysis.The ester group (COOCH3) is hydrolyzed. In the presence of an acid or a base, the ester bond can be cleaved.The ester bond may be cleaved in the presence of an base or acid. In acidic hydrolysis, the ester reacts with water to form the carboxylic acid (2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID) and methanol.In acidic hydrolysis the ester reacts to form carboxylic acid (2-CYANO- 3- (1-NAPHTHYL-ACRYLIC ACID), and methanol. In basic hydrolysis, also known as saponification, the carboxylic acid is obtained in its salt form along with methanol.In basic hydrolysis (also known as saponification), the carboxylic acids are obtained in their salt form, along with methanol.

The naphthyl group, being aromatic, has some characteristic properties.It has some distinctive properties. It can undergo electrophilic aromatic substitution reactions.It can undergo electrophilic aromatic substitute reactions. For example, nitration, sulfonation, or Friedel - Crafts reactions can potentially be carried out on the naphthyl ring, allowing for further functionalization of the molecule.The naphthyl rings can be functionalized further by nitrations, sulfonations, or Friedel-Crafts reactions.

Overall, 2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER has a combination of physical and chemical properties that make it an interesting compound for synthetic organic chemistry and potentially for applications in materials science or pharmaceuticals, depending on further derivatization and modification.Overall, 2 – CYANO – 3 – (1 – NAPHTHYL )ACRYLIC ACID+ METHYL ESTER has a combination physical and chemical characteristics that make it a compound of interest for synthetic organic chemistry. It could also be used in materials science and pharmaceuticals depending on further modification and derivatization.

What is the synthesis method of 2-CYANO-3-(1-NAPHTHYL)ACRYLIC ACID + METHYL ESTER?

The synthesis of 2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER can be achieved through the following general approach.The following general approach can be used to synthesize 2 - CYANO -3 - (1 – NAPHTHYL )ACRYLIC ACID and METHYL ESTER.
One common method is based on the Knoevenagel condensation reaction.Knoevenagel condensation is one common method. First, 1 - naphthaldehyde is used as a starting material.As a first step, 1 -naphthaldehyde will be used. It is reacted with malonic acid in the presence of a base catalyst.It is then reacted with malonic acids in the presence a base catalyst. The base can be, for example, piperidine or pyridine.The base can, for instance, be piperidine or Pyridine. These bases help in the activation of malonic acid, which has two carboxyl groups.These bases are used to activate malonic acid which has two carboxyl group.

During the reaction, the carbonyl group of 1 - naphthaldehyde undergoes a nucleophilic addition by the enolate form of malonic acid generated in the presence of the base.During the reaction the carbonyl group in 1 -naphthaldehyde undergoes nucleophilic addtion by the enolate malonic acid produced in the presence the base. This leads to the formation of an intermediate.This results in the formation of a intermediate. Subsequently, a dehydration reaction occurs.Then, a dehydration occurs. The elimination of a water molecule from the intermediate is facilitated by the reaction conditions, resulting in the formation of 2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID.The conditions of the reaction facilitate the elimination of water molecules from the intermediate, leading to the formation of 2 CYANO 3 (1 - NAPHTHYL )ACRYLIC ACID.

To obtain the methyl ester, the carboxylic acid group of 2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID needs to be esterified.Esterification of the carboxylic group of 2 – CYANO – 3 – (1 – NAPHTHYL )ACRYLIC ACID is required to obtain the methyl ester. This can be achieved by reacting the acid with methanol in the presence of an acid catalyst.This can be done by reacting the acid and methanol with an acid catalyst. Commonly used acid catalysts include sulfuric acid or p - toluenesulfonic acid.Acid catalysts are commonly used with sulfuric acid and p-toluenesulfonic acids. The acid catalyst protonates the carbonyl oxygen of the carboxylic acid, making the carbon more electrophilic.The acid catalyst protonates carbonyl oxygen in the carboxylic acids, making the carbon electrophilic. Methanol then acts as a nucleophile and attacks the carbonyl carbon.Methanol acts as a 'nucleophile' and attacks the carbonyl atom. After a series of proton transfer steps and elimination of water, 2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER is formed.After a series proton transfer steps, and the elimination of water, 2 – CYANO – 3 – (1 – NAPHTHYL )ACRYLIC ACID METHYL ESTER results.

Another possible route could involve starting from 1 - naphthylacetonitrile. Through a series of reactions such as alkylation with an appropriate aldehyde precursor followed by oxidation and esterification steps, the target compound might be synthesized.The target compound can be synthesized through a series reactions, such as alkylation of an aldehyde with an appropriate precursor, followed by oxidation or esterification. However, the Knoevenagel condensation - esterification sequence is relatively more straightforward and commonly employed in the laboratory synthesis of this type of compound.The Knoevenagel condensation-esterification sequence is a relatively simple and common method for the laboratory synthesis. The reaction conditions such as reaction temperature, reaction time, and the stoichiometry of the reactants need to be carefully optimized to achieve high yields of 2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER.To achieve high yields, the reaction conditions, such as temperature, time, and stoichiometry, must be optimized.

What is the safety information of 2-CYANO-3-(1-NAPHTHYL)ACRYLIC ACID + METHYL ESTER?

2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER, also known as methyl 2 - cyano - 3 - (1 - naphthyl)acrylate.2 – CYANO – 3 – (1 – NAPHTHYL )ACRYLIC ACID + METHYL ESTER, also known by the name methyl 2 – cyano ­ -3 - (1 naphthyl )acrylate.
Hazard identification: It may cause skin irritation.Identification of the Hazard: It can cause skin irritation. Direct contact with the skin can lead to redness, itching, and in some cases, more severe reactions.Direct contact with skin can cause redness, itching and, in some cases, even more severe reactions. It can also cause eye irritation.It can also cause irritation of the eyes. If it gets into the eyes, it may result in pain, redness, and potential damage to the eye tissues.It can cause irritation, pain, and even damage to the eye tissue if it gets in the eyes. Inhalation of its vapors or dust can irritate the respiratory tract, causing coughing, shortness of breath, and discomfort in the chest.Inhaling its dust or vapors can cause irritation of the respiratory tract. This can lead to coughing, shortness in breath, and discomfort.

First - aid measures: In case of skin contact, immediately remove contaminated clothing and wash the affected area thoroughly with plenty of water for at least 15 minutes.First-aid measures: Remove contaminated clothing immediately and wash the affected area thoroughly for at least 15 min. Seek medical advice if irritation persists. For eye contact, hold the eyelid open and rinse the eyes gently with running water for at least 15 minutes.If you have eye contact, keep the eyelids open and rinse your eyes with running water for 15 minutes. Then, seek immediate medical attention.Seek immediate medical attention. If inhaled, move the person to fresh air.If inhaled move the person outside to fresh air. If breathing is difficult, provide oxygen and call for emergency medical help.If breathing is difficult, call emergency medical help and provide oxygen.

Fire - fighting measures: This substance may be combustible.Fire-fighting measures: This substance is combustible. Use appropriate extinguishing agents such as dry chemical, carbon dioxide, or foam extinguishers in case of a fire.In the event of a fire, use appropriate extinguishing materials such as carbon dioxide, dry chemical or foam extinguishers. Avoid using water jets as they may spread the fire.Avoid using water jets, as they can spread the fire. Firefighters should wear self - contained breathing apparatus and appropriate protective clothing to prevent exposure.Firefighters must wear self-contained breathing apparatus and protective clothing to avoid exposure.

Handling and storage: When handling, use proper personal protective equipment including gloves, safety glasses, and a lab coat.Handling and Storage: Use personal protective equipment when handling. This includes gloves, safety sunglasses, and a lab jacket. Avoid generating dust or vapors.Avoid generating dust and vapors. Keep the container tightly closed when not in use.When not in use, keep the container tightly shut. Store in a cool, dry, well - ventilated area away from heat sources, ignition sources, and incompatible substances.Store in a cool and dry area, away from heat sources or ignition sources. Incompatible materials may include strong acids, strong bases, and oxidizing agents.Incompatible materials can include strong acids, bases and oxidizing agents.

Accidental release measures: In case of a spill, first, isolate the area to prevent the spread.Accidental release measures. In the event of an accident, you should first isolate the area in order to prevent it from spreading. Wear appropriate protective gear. Absorb the spill with an inert absorbent material like sand or vermiculite.Absorb spills with a material that is inert, such as sand or Vermiculite. Then, collect the contaminated material and place it in a proper waste container for disposal according to local regulations.Collect the contaminated material, and dispose of it according to local regulations. Thoroughly clean the spill area to remove any remaining traces.Clean the spill area thoroughly to remove all traces.

Where can I find 2-CYANO-3-(1-NAPHTHYL)ACRYLIC ACID + METHYL ESTER for purchase?

2 - CYANO - 3 - (1 - NAPHTHYL)ACRYLIC ACID + METHYL ESTER is a chemical compound.A chemical compound is 2 - CYANO -3 - (1 – NAPHTHYL )ACRYLIC ACID+ METHYL ESTER. Here are some places where you might be able to find it for purchase.Here are a few places you may be able purchase it.
First, chemical suppliers are a common option.Chemical suppliers are one of the most common options. Well - known chemical distributors like Sigma - Aldrich (now part of Merck), Alfa Aesar, and TCI Chemicals usually have a vast inventory of a wide range of chemical compounds.Well-known chemical distributors such as Sigma - Aldrich, Alfa Aesar and TCI Chemicals have a large inventory of chemical compounds. These companies have an online presence where you can search for the specific compound.These companies have a website where you can search by compound. Their websites often provide detailed product information, including purity levels, packaging options, and pricing.Their websites provide detailed information about their products, including packaging options, pricing, and purity levels. However, you may need to register as a customer, which could involve providing details about your organization or research purpose.You may have to register as a client, which might require you to provide details about your organization, or research purpose. Some of these suppliers may require a business or academic account to make purchases, especially for larger quantities.Some suppliers may require an academic or business account to purchase large quantities.

Another possibility is to check with local chemical supply houses.Check with local chemical suppliers. In many industrial areas or near universities, there are local companies that supply chemicals.Local chemical companies are located in many industrial areas and near universities. They may be more flexible in terms of smaller quantity orders and can sometimes offer more personalized service.They may be more flexible with smaller orders and offer a more personalized service. You can find them through local business directories or by asking for recommendations from local research institutions, chemical laboratories, or industrial facilities that work with similar chemicals.You can find them in local business directories, or by asking local research institutions, laboratories, or industrial facilities who work with similar chemicals for recommendations.

Online marketplaces that deal with chemicals can also be a source.Online marketplaces dealing with chemicals are also a good source. But when using such platforms, extra caution is needed.When using such platforms, you should exercise extra caution. Ensure that the sellers are legitimate and follow all safety and regulatory requirements.Verify that the sellers follow all safety and regulatory regulations. Some online platforms may have user reviews or ratings that can help you assess the reliability of the seller.Some online platforms have user reviews and ratings that you can use to assess the reliability of a seller.

If you are associated with an academic institution or a research organization, the institution's procurement department may be able to assist in sourcing the compound.If you're affiliated with an academic institution, or a research organisation, the institution may be able assist you in sourcing the compound. They often have established relationships with chemical suppliers and can handle the purchasing process, taking care of aspects like compliance with safety regulations and proper documentation.They have relationships with chemical suppliers, and can handle the buying process. They can also take care of safety regulations and proper paperwork.

It's important to note that when purchasing such chemical compounds, you need to comply with all relevant laws and regulations.When purchasing chemical compounds, it is important to comply with all applicable laws and regulations. This includes proper handling, storage, and transportation requirements.This includes the proper handling, storing, and transporting requirements. Additionally, make sure you have the appropriate safety equipment and facilities to deal with the chemical once it is in your possession.Ensure you have the right safety equipment and facilities in place to handle the chemical once you obtain it.