1 Ethoxy 2 3 Difluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-ethoxy-2,3-difluorobenzene
Chemical Formula C8H8F2O
Molecular Weight 158.145
Appearance Liquid (expected, based on similar compounds)
Solubility In Water Insoluble (aromatic ethers are generally hydrophobic)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether, dichloromethane
Chemical Formula C8H8F2O
Molecular Weight 158.145
Chemical Formula C8H8F2O
Molecular Weight 158.145 g/mol
Appearance liquid (presumably, based on similar compounds)
Solubility In Water likely low, due to non - polar benzene ring
Solubility In Organic Solvents soluble in common organic solvents like ethanol, ether
Chemical Formula C8H8F2O
Molecular Weight 158.145
Appearance Colorless to light yellow liquid
Boiling Point Around 180 - 190 °C
Density Approx. 1.1 - 1.2 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Vapor Pressure Low at room temperature
Flash Point Approx. 60 - 70 °C
FAQ

What are the main uses of 1-ethoxy-2,3-difluorobenzene?

1-Ethoxy-2,3-difluorobenzene (1-ethoxy-2,3-difluorobenzene) is also an organic compound. Its main uses cover a wide range of chemical fields.

In the process of organic synthesis, this compound is often used as a key intermediate. Its structure is unique, and ethoxy and difluorine atoms give it special reactivity. It can be used through many reactions, such as nucleophilic substitution reactions, to introduce other functional groups, and then build a multi-complex organic molecular structure. Chemists can use this to create a variety of high-value-added fine chemicals, such as pharmaceuticals, pesticides, material additives, etc.

In the field of medicine, 1-ethoxy-2,3-difluorobenzene may be the cornerstone of the synthesis of specific drugs. Because its structure can fit with specific biological targets, it is modified and derived by organic synthesis, and it is expected to obtain molecules with specific pharmacological activities, or used in the treatment of diseases, such as antibacterial, antiviral, anti-tumor, etc., for human health and well-being.

Pesticide creation is also common in its shadow. After rational molecular design and synthesis optimization, pesticides made from 1-ethoxy-2,3-difluorobenzene as the starting material may have high efficiency, low toxicity and environmentally friendly characteristics. It can effectively prevent and control crop diseases and pests, ensure crop yield and quality, and is of great significance to the sustainable development of agriculture.

Furthermore, in the field of materials science, it may be able to participate in the preparation of functional materials. After specific reaction polymerization, or materials with special optical and electrical properties, such as organic optoelectronic materials, contribute to the development of electronic and optical devices.

In short, 1-ethoxy-2,3-difluorobenzene has important uses in many fields such as chemical industry, medicine, pesticides, materials, etc., and promotes technological innovation and product upgrades in various fields.

What are the physical properties of 1-ethoxy-2,3-difluorobenzene?

1-Ethoxy-2,3-difluorobenzene is also an organic compound. Its physical properties are of great research value.

Looking at its properties, under normal temperature and pressure, or as a colorless liquid, clear and transparent, such as mirror water, or light yellow, slightly yellow color, its state is stable, no spontaneous significant changes.

As for its boiling point, due to the intermolecular force, it is about a specific temperature range. The interaction between the ethoxy group in the molecule and the difluorobenzene ring makes the intermolecular attractive force different, causing the boiling point to be different from the common simple benzene compounds. It is speculated that its boiling point may be around [X] ° C, but this value varies with factors such as environmental pressure.

Melting point is also an important physical property. The arrangement and interaction of molecules are fully apparent at low temperatures. When the temperature drops to a certain extent, the molecular movement gradually slows down, the arrangement tends to be orderly, and finally becomes a solid state. Its melting point is about [Y] ° C. This temperature defines the transformation of its solid-liquid and is a key node in material research.

In terms of density, 1-ethoxy-2,3-difluorobenzene has its own specific value. Due to the compactness of its molecular composition and structure, the density is about [Z] g/cm ³. This value reflects the mass per unit volume of the substance. Compared with other similar compounds, its mass distribution characteristics can be seen.

Solubility is another important item. In organic solvents, such as ethanol and ether, due to the principle of similar miscibility, they may have good solubility and can be miscible with organic solvents to form a uniform system. However, in water, due to its large difference in molecular polarity from water molecules, the solubility may be poor, only slightly soluble or insoluble, so that when water is mixed with it, it is often stratified.

In addition, its volatility cannot be ignored. Although it is not a highly volatile substance, under appropriate temperature and air circulation environment, molecules escape from the liquid surface and disperse in the surrounding space. This property is related to its stability and application scenarios in the environment.

In summary, the physical properties of 1-ethoxy-2,3-difluorobenzene are complex and unique, which lays the foundation for its research and application in the field of chemistry.

Is 1-ethoxy-2,3-difluorobenzene chemically stable?

1 - ethoxy - 2,3 - difluorobenzene is an organic compound. The stability of its chemical properties needs to be discussed from a multi-end perspective.

First look at its chemical bonds. This compound contains carbon-fluorine (C-F) bonds, carbon-oxygen (C-O) bonds and carbon-carbon (C-C) bonds, etc. For C-F bonds, due to the extremely high electronegativity of fluorine, the bond energy is quite large, about 485kJ/mol. This bond is extremely difficult to break, which gives molecular stability to a certain extent. Similarly, the C-O bond energy is not low, about 358kJ/mol, which can enhance the stability of molecular structure. < Br >
Second observation of its electronic effect. The benzene ring has a conjugated system, and the electron cloud can be delocalized, which reduces the molecular energy and increases the stability. The fluorine atoms at positions 2 and 3 have a strong electron-absorbing induction effect (-I), which can reduce the electron cloud density of the benzene ring and make it difficult for electrophilic substitution reactions to occur. This is also a stable characterization. However, the electron-absorbing induction effect may affect the carbon-oxygen bond at the ortho-site, reducing the electron cloud density on the oxygen atom, but overall, it does not significantly damage its stability.

Furthermore, its spatial structure also plays a role. The steric resistance between fluorine atoms and ethoxy groups affects the intermolecular interactions. The ethoxy group is large in size, or makes the molecular arrangement slightly looser, but the fluorine atom is small, and the effect of steric hindrance is limited, which does not pose a serious threat to the stability of the molecular core structure.

In summary, 1-ethoxy-2,3-difluorobenzene is relatively stable under general conditions due to the above chemical bonds, electronic effects and spatial structure. Its structure and properties may change under specific extreme conditions, such as high temperature, strong acid-base or strong oxidant.

What are the synthesis methods of 1-ethoxy-2,3-difluorobenzene?

The synthesis method of 1-ethoxy-2,3-difluorobenzene is not detailed in the ancient book "Tiangongkai", but the current chemical synthesis method can be done in the following ways.

First, 2,3-difluorophenol is used as the starting material. This phenol is first etherified with ethanol under the action of an acidic catalyst such as concentrated sulfuric acid to obtain the target product. Concentrated sulfuric acid can promote the dehydration and condensation of the hydroxyl group of phenol and the hydroxyl group of ethanol, but the temperature needs to be controlled during the reaction. If the temperature is too high, it is easy to cause side reactions, such as dehydration of ethanol to ethylene. During the reaction, the two are mixed evenly. When the reaction number is stirred at an appropriate temperature (about 120-140 ° C), the product is purified by distillation, extraction, drying and other steps.

Second, 2,3-difluorobromobenzene and sodium ethanol are used as raw materials. This is a nucleophilic substitution reaction. The bromine atom of 2,3-difluorobromobenzene has high activity, and the ethoxy negative ion of sodium ethanol has strong nucleophilicity. The two react at a certain temperature (about 80-100 ° C) in an appropriate solvent such as DMF (N, N-dimethylformamide). DMF can dissolve both and promote the reaction. After the reaction is completed, the pure 1-ethoxy-2,3-difluorobenzene is obtained by separation and purification methods, such as column chromatography.

Third, 2,3-difluorobenzoic acid is used as the starting material, and it is first reduced to 2,3-difluorobenzyl alcohol, which can be used as a strong reducing agent such as lithium aluminum hydride. After 2,3-difluorobenzyl alcohol is reacted with hydrobromic acid to obtain 2,3-difluorobenzyl bromide, which is then reacted with sodium ethyl alcohol to form the target product through nucleophilic substitution. This route step is slightly complicated, but the reaction conditions at each step are relatively mild, and the products at each step are also easier to separate and purify.

What is the price range of 1-ethoxy-2,3-difluorobenzene in the market?

It is difficult to determine the price range of 1-ethoxy-2,3-difluorobenzene in the market. The price of this substance often varies due to various factors.

First, the scale of production is related to the price. If the producer operates widely, the purchase and purchase of materials is large, and the technical skills are appropriate, the cost may be reduced, and its sale may be low. On the contrary, if the scale of production is narrow and the cost is high, the price will be high.

Second, the price of raw materials is also an important factor. The price of 1-ethoxy-2,3-difluorobenzene is also stable if the raw materials are easy to obtain and the price is flat. If the raw materials are scarce and difficult to find, the price will rise, and the price of the product will also rise.

Third, the supply and demand of the city is the key. If you need more supply and less supply, you may increase the price to make a profit; if the supply exceeds the demand, it will be sold quickly, or the price will be reduced.

Fourth, the quality is also related to the price. Those who are of high quality have strict inspection and testing, long warranty period, and the price is higher than those who are of poor quality.

To sum up, in today's city, the price of 1-ethoxy-2,3-difluorobenzene per kilogram may be between hundreds and thousands of yuan. However, this is only a rough estimate. The market conditions are ever-changing. To know the exact price, you need to consult the producers, dealers, or refer to the real-time market conditions of the city.