2 Ethoxy 4 6 Difluoropyrimidine
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Ethoxy-4,6-Difluoropyrimidine
Name 2-Ethoxy-4,6-Difluoropyrimidine
Molecular Formula C6H6F2N2O
Molecular Weight 162.12
Solubility Soluble in common organic solvents like dichloromethane, chloroform, ethyl acetate; limited solubility in water
Purity Can be produced in high purity grades (e.g., 95%+, depending on production method)
Stability Stable under normal conditions, but may react with strong acids, bases, or reducing/oxidizing agents
Chemical Formula C6H6F2N2O
Molecular Weight 162.12
Appearance Colorless to light yellow liquid or solid
Solubility In Water Poorly soluble in water (estimated as fluoropyrimidine derivatives usually have low water solubility)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (general property of similar organic compounds)
Purity Can be obtained in various purity levels depending on synthesis and purification methods, usually high - purity grades are desired for most applications
Chemical Formula C6H6F2N2O
Molecular Weight 160.12
Appearance Typically a solid (appearance may vary based on purity and conditions)
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform (qualitative, quantitative data needs experiment)
Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
FAQ

2-Ethoxy-4, what is the chemical nature of 6-Difluoropyrimidine

2-Ethoxy-4,6-difluoropyrimidine is one of the organic compounds. It has specific chemical properties.

The physical properties of this compound are either solid or liquid at room temperature, but the specific form depends on its purity and external conditions. Its melting point, boiling point and other properties are quite critical in the experimental design and operation of organic synthesis. The cap melting point can help determine its purity. If there are few impurities, the melting point is sharp and close to the theoretical value; the boiling point is related to the separation and purification steps, and it can be separated from the mixture by distillation according to the difference in boiling points.

In terms of chemical properties, its pyrimidine ring is aromatic, which makes the compound have a certain stability. The fluorine atom and ethoxy group on the ring have a great influence on its reactivity. Fluorine atoms have strong electronegativity, which can reduce the electron cloud density on the ring and enhance the activity of electrophilic substitution. For example, under specific conditions, it can substitution with electrophilic reagents, and the substitution check point has a certain selectivity due to the positioning effect of fluorine atoms. Ethoxy is the power supply group, which also affects the electron cloud density distribution of the pyrimidine ring, and can change the reaction path and rate in some reactions.

2-ethoxy-4,6-difluoropyrimidine can participate in many organic reactions. In the field of synthetic chemistry, it may be used as a key intermediate to react with different reagents to build complex organic molecular structures. In the field of medicinal chemistry, such structures either exhibit biological activity due to their unique chemical properties, or are potential drug lead compounds, which are expected to be modified and optimized to develop new drugs. However, the research and application of their chemical properties still require fine experiments and in-depth exploration by chemists in order to fully explore their potential and contribute to the fields of organic synthesis and pharmaceutical research and development.

2-Ethoxy-4, what are the main uses of 6-Difluoropyrimidine

2-Ethoxy-4,6-difluoropyrimidine is a key compound in the field of organic synthesis. It has a wide range of uses and plays an indispensable role in many important fields.

First in the field of medicine, this compound is often a key intermediate for the creation of new drugs. Because of its unique chemical structure, it can interact with specific targets in organisms, thus exhibiting a variety of biological activities such as antibacterial and antiviral. Taking antibacterial drugs as an example, by modifying their structures, they can precisely act on the key metabolic pathways of bacteria, inhibit bacterial growth and reproduction, and open up a new path for the development of antibacterial drugs.

Furthermore, in the field of pesticides, 2-ethoxy-4,6-difluoropyrimidine also occupies an important position. It can be used as a synthetic raw material for high-efficiency pesticides to prepare insecticides, fungicides, etc. Because of its specific killing effect on some pests and bacteria, it can effectively improve the yield and quality of crops, and reduce the negative impact of pesticides on the environment, which is in line with the current needs of green agriculture development.

In addition, in the field of materials science, this compound may be able to participate in the synthesis of functional materials. With its special physical and chemical properties, it endows materials with unique properties such as fluorescence and conductivity, providing new opportunities for the development of new functional materials.

2-ethoxy-4,6-difluoropyrimidine plays an important role in the fields of medicine, pesticides and materials science. With the continuous progress of science and technology, its application prospects will also be broader.

2-Ethoxy-4, what are the synthesis methods of 6-Difluoropyrimidine

There are various ways to prepare 2-ethoxy-4,6-difluoropyrimidine.

First, 4,6-dichloro-2-ethoxy pyrimidine is used as the starting material to interact with the fluorinating agent. This fluorinating agent can be selected from potassium fluoride, cesium fluoride, etc. During the reaction, an organic solvent such as N, N-dimethylformamide (DMF), dimethyl sulfoxide (DMSO), etc. is often required to stir the reaction at an appropriate temperature. The temperature may be controlled between 60 ° C and 150 ° C. After several or even ten hours, the target product can be obtained after post-treatment, such as extraction, distillation, column chromatography, etc. < Br >
Second, starting from 2-hydroxy-4,6-difluoropyrimidine, it is reacted with ethanol and an appropriate condensing agent. The condensing agent can be selected such as concentrated sulfuric acid, p-toluenesulfonic acid and the like. Under the condition of heating and refluxing, the reaction number is followed by the steps of neutralization, separation and purification, and 2-ethoxy-4,6-difluoropyrimidine can also be prepared.

Or, the corresponding pyrimidine ring derivative can be reacted in multiple steps to construct ethoxy and difluoro substituents. The ethoxy group is introduced first, and then the fluorine atom is introduced, or vice versa. Each step of the reaction requires careful regulation of the reaction conditions, such as temperature, pH, reaction time, etc., according to the characteristics of the reactants. After multiple separation and purification operations, the final product is obtained. These methods have their own advantages and disadvantages. In actual preparation, when considering the availability of raw materials, cost, yield and many other factors, the choice is made.

2-Ethoxy-4, 6-Difluoropyrimidine What are the precautions in storage and transportation?

2-Ethoxy-4,6-difluoropyrimidine is an important intermediate in organic synthesis. There are many matters to be paid attention to during storage and transportation.

Its nature is active, and the first environment is dry when stored. If the environment is humid, moisture is easy to react with it, causing it to deteriorate, losing its original chemical properties and reactivity, affecting subsequent use. Choose a dry, well-ventilated place, away from water sources and water vapor.

Temperature is also critical. This substance is sensitive to temperature, and high temperature may cause decomposition or accelerate chemical reactions, resulting in damage to quality. Usually should be stored in a cool place, the temperature should be maintained in a specific range, generally 2-8 ℃ is better, avoid direct sunlight, in case the heat of sunlight increases the temperature and affects its stability.

In addition, storage containers also need to pay attention to. Containers of suitable materials should be selected to ensure that they do not chemically react with 2-ethoxy-4,6-difluoropyrimidine, and have good sealing to prevent them from volatilizing or reacting with external air components. Containers made of glass or specific plastic materials can only be used after being inspected and suitable.

When transporting, the packaging must be stable. Because it is inevitable to be bumpy and vibrated during transportation, if the packaging is not strong, it is easy to cause damage to the container and cause material leakage. It needs to be properly packaged with shock-proof and pressure-resistant materials to ensure transportation safety.

The transportation environment should also be kept dry and cool like storage. Transportation vehicles need to have good heat insulation and ventilation equipment to avoid transportation during high temperature periods and reduce the impact of temperature and humidity on them.

And transportation personnel should be familiar with the characteristics of this substance and emergency treatment methods. If there is an accident such as leakage on the way, they can respond in time and correctly to reduce hazards. In this way, the quality of 2-ethoxy-4,6-difluoropyrimidine during storage and transportation can be guaranteed, and it is safe and worry-free.

2-Ethoxy-4, what is the market outlook for 6-Difluoropyrimidine?

2-Ethoxy-4,6-difluoropyrimidine, which is a crucial fine chemical in the field of organic synthesis. Looking at its market prospects, it is like the beginning of a star, showing a booming trend.

In the field of medicine, due to its unique chemical structure and activity, it is like a shining cornerstone in the journey of innovative drug development. Many scientific research teams have focused on this, dedicated to exploring its potential pharmacological activities such as antibacterial, antiviral, and anti-tumor. Taking the development of anti-tumor drugs as an example, researchers hope to modify its structure to create new anti-cancer drugs with stronger targeting, better efficacy and fewer side effects. In time, when the research and development results are realized, it will definitely bring a new dawn to cancer patients, and the market demand will also grow.

In the field of pesticides, 2-ethoxy-4,6-difluoropyrimidine is a key intermediate for the creation of new pesticides. With the increasing emphasis on food safety and environmental protection around the world, the development of high-efficiency, low-toxicity and environmentally friendly pesticides has become a general trend. The characteristics of this compound can just meet this demand, and it is expected to give rise to a series of new insecticides, fungicides or herbicides. Once successfully developed and popularized, it will definitely occupy a place in the pesticide market, and the market potential is limitless.

Looking at the development trend of the industry, with the continuous progress of science and technology, organic synthesis technology is also constantly innovating. The synthesis process for 2-ethoxy-4,6-difluoropyrimidine is also evolving towards a more green, efficient and economical direction. If more advanced synthesis routes can be developed, production costs will be greatly reduced, product quality and competitiveness will be improved. In this way, its market share is expected to be further expanded in both domestic and international markets.

In summary, 2-ethoxy-4,6-difluoropyrimidine, with its broad application prospects in the field of medicine and pesticides, as well as the favorable trend of industry development, is like a giant ship setting sail, sailing towards a more brilliant future in the market. Its market prospect is very promising, and it is expected to become a new economic growth point in related fields.