4 Methyl 2 3 5 6 Tetrafluorobenzyl Alcohol
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-methyl-2,3,5,6-tetrafluorobenzyl alcohol
Chemical Formula C8H6F4O
Molar Mass 194.126 g/mol
Appearance Colorless to light yellow liquid
Boiling Point 190 - 192 °C
Melting Point N/A
Density 1.34 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents
Flash Point 76 °C
Purity Typically high - purity in commercial products
Chemical Formula C8H6F4O
Molecular Weight 194.126
Appearance Typically a colorless to light - colored liquid
FAQ

What are the main uses of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol?

4-Methyl-2,3,5,6-tetrafluorobenzyl alcohol is an important chemical substance in the field of organic synthesis. It has a wide range of uses and is of great value in the synthesis of medicines.

Because of the delicate medical chemistry, the creation of many drugs requires delicate molecular construction. The special structure of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol, the ingenious combination of fluorine atoms and methyl groups, enables it to participate in a variety of chemical reactions to build the molecular framework required for drug activity. By means of chemical reaction, it can be connected to the drug molecular system, or affect the lipophilicity of the drug, help it more easily penetrate the biofilm, improve the absorption efficiency of the drug; or adjust the electron cloud distribution of the drug molecule, affect its interaction with biological targets, enhance the activity and selectivity of the drug, so as to help create new drugs with high efficiency and low side effects.

In the field of pesticide synthesis, this substance is also important. The efficacy of pesticides is related to the prosperity of agriculture. 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol can be used as a key intermediate, which can be integrated into pesticide molecules through a series of chemical transformations. The introduction of fluorine atoms can often improve the biological activity, stability and environmental compatibility of pesticides. It can make pesticides more effective in inhibiting the growth and reproduction of pests and pathogens, and at the same time degrade quickly in the environment, reduce residues, reduce the adverse impact on the ecological environment, and ensure the quality and safety of agricultural products. It is of great significance for the sustainable development of modern agriculture.

In addition, in the field of materials science, it can also be seen. With the advance of science and technology, the need for special performance materials is increasing. 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol can participate in the synthesis of material monomers, and through polymerization and other reactions, give the material unique properties. For example, fluoropolymer materials, due to the characteristics of fluorine atoms, often have excellent chemical corrosion resistance, low surface energy, and high temperature resistance. Materials made from this material can be used in high-end fields such as electronics and aerospace to meet their strict requirements for the special properties of materials.

What are the physical properties of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol

4 - methyl - 2,3,5,6 - tetrafluorobenzyl alcohol (4 - methyl - 2,3,5,6 - tetrafluorobenzyl alcohol) is an organic compound with specific physical properties.

Its properties are usually colorless to light yellow liquids or solids. Due to the molecular structure containing fluorine atoms and benzyl alcohol groups, the intermolecular force is unique. The melting point and boiling point have a great influence on the intermolecular force due to the high electronegativity of fluorine atoms. Generally speaking, the melting point is about [X] ° C, and the boiling point is about [X] ° C. The specific values are determined by experiments. < Br >
In terms of solubility, it has good solubility in organic solvents such as ethanol, ether, and dichloromethane. Because the organic groups in the molecule have similar chemical properties to organic solvents, they are mutually soluble according to the principle of "similar miscibility". However, the solubility in water is poor, because the non-polar organic part accounts for a large proportion, and the force between water molecules is weak.

The density is larger than that of water, about [X] g/cm ³, which is determined by its molecular composition and structure. The fluorine atom has a large relative atomic weight, which increases the molecular weight and causes a high density.

4 - methyl - 2,3,5,6 - tetrafluorobenzyl alcohol has a special odor, the odor is weak and irritating, because of its special chemical structure, it interacts with olfactory receptors in this odor.

In addition, this compound has a certain volatility. At room temperature and pressure, some molecules can escape from the liquid surface and enter the gas phase, but its volatility is weaker than that of common low-boiling organic solvents. Due to the existence of certain forces between molecules, molecular escape is restricted.

Is 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol chemically stable?

4-Methyl-2,3,5,6-tetrafluorobenzyl alcohol. The stability of the chemical properties of this substance depends on the comprehensive consideration of its molecular structure and the environment in which it is located.

Looking at its structure, the introduction of fluorine atoms has a great impact on its chemical properties. Fluorine is an element with strong electronegativity. In this compound, many fluorine atoms are distributed around the benzene ring. Due to the strong electronegativity of fluorine, it will have a significant effect on the electron cloud density of the benzene ring, reducing the electron cloud density of the benzene ring. As a result, the activity of the benzene ring to participate in the electrophilic substitution reaction decreases, because the electrophilic substitution reaction usually relies on the higher electron cloud density of the benzene ring to attract electrophilic reagents.

As far as the structural part of benzyl alcohol is concerned, the hydroxyl group is connected to the benzyl group. Because the electron cloud density of the benzene ring is affected by the fluorine atom, the electron cloud density of the carbon atom connected to the hydroxyl group also changes, which in turn affects the polarity of the oxygen-hydrogen bond in the hydroxyl group. This change may cause the activity of the hydroxyl hydrogen atom to be different. Compared with the benzyl alcohol without fluorine substitution, or when the hydroxyl group-related reactions occur, such as esterification, dehydration, etc., it shows a different activity.

However, in terms of its stability, it depends on the environment in which it is located. If it is in an environment at room temperature and pressure without the action of special chemical reagents, its carbon-fluorine bond energy is quite high, and it is not easy to break under general conditions, so However, its structure may change under conditions such as high temperature, strong oxidizing agent or specific catalyst. In case of strong oxidizing agent, the hydroxyl group may be oxidized to an aldehyde group or even a carboxyl group; under high temperature and suitable catalyst, the carbon-fluorine bond may also break and react.

In summary, the chemical stability of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol cannot be generalized, and it needs to be comprehensively determined according to the specific structural characteristics and external environmental conditions.

What is the preparation method of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol

The preparation of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol is an important issue in the field of organic synthesis. Common preparation methods can be obtained by reducing 4-methyl-2,3,5,6-tetrafluorobenzoic acid and its derivatives.

First, 4-methyl-2,3,5,6-tetrafluorobenzoic acid is used as the starting material, and a strong reducing agent such as lithium aluminum hydride (LiAlH) is selected. This reaction needs to be carried out in an anhydrous organic solvent such as anhydrous tetrahydrofuran (THF). Slowly add lithium aluminum hydride to the THF solution containing 4-methyl-2,3,5,6-tetrafluorobenzoic acid and stir the reaction at low temperature. Lithium aluminum hydride has strong reducing properties, and can reduce carboxyl groups (-COOH) to hydroxymethyl groups (-CH 2O OH) to obtain the target product 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol. After the reaction, an appropriate amount of water or dilute acid should be carefully added to decompose excess aluminum lithium hydride, and the product should be purified by extraction, washing, drying and column chromatography.

Second, if 4-methyl-2,3,5,6-tetrafluorobenzoate is used as raw material, a relatively mild reducing agent, sodium borohydride (NaBH), can be selected. This reaction is usually carried out in alcoholic solvents such as methanol or ethanol. Sodium borohydride can reduce ester groups (-COOR) to hydroxymethyl groups under specific conditions. First, 4-methyl-2,3,5,6-tetrafluorobenzoate is dissolved in an alcohol solvent, an appropriate amount of sodium borohydride is added, and the reaction is stirred at an appropriate temperature. The reaction process can be monitored by thin-layer chromatography (TLC). After the reaction is completed, pure 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol is obtained through acidification, extraction, drying and distillation.

In addition, there are also methods for the preparation of halogenated aromatics by nucleophilic substitution, reduction and other multi-step reactions. However, this route is cumbersome and the yield may be affected. Therefore, the reduction method with benzoic acid and its derivatives is more commonly used because it is relatively simple and can effectively obtain the target product 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol.

What is the price range of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol on the market?

The price range of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol in the market is not easy to determine. The price of this compound often depends on many factors, such as the abundance of raw materials, the difficulty of preparation, the amount of market demand, and the policies of producers.

If the price of chemical industry fluctuates in the past, if the raw materials are abundant and easier to prepare, the price often tends to be flat. Let the raw materials of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol be abundant, and the preparation method is simple, the energy consumption is quite low, and the market demand is not urgent, then the price may be in the lower domain. However, if the raw materials are rare and the preparation process is complicated, exquisite equipment and complicated processes are required, and the market seeks a sharp increase, the price will rise.

Looking at the chemical market conditions, the price of similar fine chemicals fluctuates greatly. In ordinary times, the price of such fine chemical raw materials per kilogram may be in the hundreds of yuan. In case of a shortage of raw materials, or due to environmental regulations, the price may soar to more than 1,000 yuan per kilogram. Or due to the advent of new production methods, the production efficiency will increase greatly, and the price may also drop to a lower level.

It is important to note that the market price of 4-methyl-2,3,5,6-tetrafluorobenzyl alcohol may fluctuate between a few hundred and a thousand yuan per kilogram depending on the current situation. To obtain an accurate price, it is necessary to consult the suppliers of chemical materials, or carefully check the recent market information to be sure.