3 Phenoxy 4 Fluoro Benzyl Alcohol
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
3-(Phenoxy)-4-fluoro-benzyl alcohol
Chemical Formula C13H11FO2
Molar Mass 218.224 g/mol
Appearance Solid (presumed, typical for such compounds)
Solubility In Water Low (due to non - polar aromatic parts)
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, dichloromethane
Vapor Pressure Low (for a solid at room temperature)
Chemical Formula C13H11FO2
Molecular Weight 218.22
Appearance [describe appearance if known]
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Solubility In Water [describe solubility if known]
Solubility In Organic Solvents [describe solubility if known]
Density [value if known] g/cm³
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FAQ

What are the chemical properties of 3- (Phenoxy) -4-fluoro-benzyl alcohol?

3- (phenoxy) -4-fluorobenzyl alcohol, this is an organic compound. Its physical properties are either solid or liquid under normal conditions. Due to the hydroxy group and benzene ring structure in the molecule, its melting point and boiling point are affected by intermolecular forces. Hydroxyl groups can cause hydrogen bonds to form between molecules, which increases the melting point and boiling point; benzene ring structure increases the intermolecular van der Waals force, which also affects the melting boiling point. However, the exact melting point still needs to be determined experimentally or consulted professional data. In terms of solubility, phenoxy groups and fluorine atoms in the molecule have certain hydrophobicity, while hydroxyl groups have hydrophilicity. Therefore, in organic solvents such as ethanol, ethyl ether, and dichloromethane, it may have good solubility; in water, its solubility may be limited, but because hydroxyl groups can form hydrogen bonds with water, or dissolve to a certain extent.

In terms of its chemical properties, hydroxyl groups are active and can participate in a variety of chemical reactions. Esterification reactions can occur, and corresponding ester compounds can be formed with carboxylic acids or acyl chlorides under the action of catalysts. This reaction is an important method for preparing esters. Hydroxyl groups can also be oxidized. If a suitable oxidant is used, they can be oxidized to an aldehyde group or a carboxyl group. Furthermore, substitution reactions can occur on the benzene ring. Because of its electron cloud density, electrophilic reagents can attack the benzene ring, and reactions such as halogenation, nitration, and sulfonation can occur. The oxygen atoms in the phenoxy group can provide lone pairs of electrons, which increases the density of electron clouds in the o and para-sites of the benzene ring, making these positions more prone to electrophilic substitution reactions. At the same time, although fluorine atoms are relatively inactive, they may

What are the main applications of 3- (Phenoxy) -4-fluoro-benzyl alcohol?

3- (phenoxy) -4 -fluoro-benzyl alcohol is an organic compound. It has a wide range of uses in the field of medicinal chemistry and can be a key intermediate for the creation of drugs. Drug creation is to find, develop and prepare new compounds with therapeutic efficacy. This compound may play an indispensable role in the synthesis of drug molecules with specific biological activities. Through its special chemical structure, it can interact with specific targets in organisms to demonstrate therapeutic effects.

In the field of materials science, it also has its uses. Or can participate in the preparation of materials with special properties, such as in the synthesis process of polymer materials, adding this compound, or can give the material such as special optical and electrical properties, or enhance its mechanical properties, stability, etc., making it suitable for electronic devices, optical materials and many other aspects.

In the field of agricultural chemistry, it may also have potential applications. Or it can be used as a raw material for the synthesis of new pesticides. With its chemical properties, it can prepare pesticide products that are efficient in pest control, environmentally friendly, and low toxicity, in order to ensure crop yield and quality, while reducing the negative impact on the ecological environment. In short, 3- (phenoxy) -4 -fluoro-benzyl alcohol has important application value in many fields such as medicine, materials, agriculture, etc. It is a compound that cannot be underestimated.

What are the synthesis methods of 3- (Phenoxy) -4-fluoro-benzyl alcohol?

The synthesis method of 3- (phenoxy) -4-fluorobenzyl alcohol has always been the most important in the field of organic synthesis. There are several methods for the synthesis of this compound.

One of them can be prepared by reduction of 3- (phenoxy) -4-fluorobenzoic acid. Lithium aluminum hydride or sodium borohydride are often used as reducing agents. Taking lithium aluminum hydride as an example, in an anhydrous organic solvent such as anhydrous tetrahydrofuran, lithium aluminum hydride is slowly added to a solution containing 3- (phenoxy) -4-fluorobenzoic acid at low temperature. The two react and then hydrolyze to obtain the target product 3- (phenoxy) -4-fluorobenzyl alcohol. In this process, lithium aluminum hydride has strong reduction ability and complete reaction. However, strict anhydrous and anaerobic conditions are required, and the operation requirements are quite high.

Second, 3- (phenoxy) -4-fluorobenzyl halide is used as raw material, which can be obtained by nucleophilic substitution reaction. For example, 3- (phenoxy) -4-fluorobenzyl chloride and nucleophilic reagents, such as sodium hydroxide aqueous solution, are used at appropriate temperatures and reaction times. The chlorine atom is replaced by a hydroxyl group to generate 3- (phenoxy) -4-fluorobenzyl alcohol. The raw materials for this method are relatively easy to obtain, and the reaction conditions are relatively mild. Therefore, it is necessary to pay attention to the amount of nucleophilic reagents and the control of the reaction temperature to avoid side reactions.

Furthermore, phenoxy fluorobenzene and formaldehyde are used as starting materials. Under the action of suitable catalysts, the condensation reaction can also be obtained. If the two condensate in the presence of basic catalysts, the target product can be obtained after appropriate treatment. The starting materials of this route are common, but the selection of catalysts and the optimization of reaction conditions are crucial, which are related to the yield and purity of the product.

Synthesis of 3- (phenoxy) -4-fluorobenzyl alcohol has advantages and disadvantages. The appropriate synthesis method needs to be weighed according to actual needs, such as raw material availability, reaction conditions, product purity and yield.

What is the market outlook for 3- (Phenoxy) -4-fluoro-benzyl alcohol?

3- (phenoxy) -4 -fluoro-benzyl alcohol, this substance is worth exploring in the current market prospect. Looking at the current chemical industry, the demand for fine chemicals is increasing day by day. Such compounds have potential uses in medicine, pesticides and materials science due to their unique chemical structures.

In the field of medicine, due to its specific functional group combination, it may be used as an intermediate for the synthesis of new drugs. With the in-depth study of disease mechanisms, the demand for the development of new specific drugs has surged. Such novel compounds may provide new opportunities for the development of innovative drugs, and the market potential is considerable.

In the field of pesticides, the existence of fluorine atoms and phenoxy groups may endow the compounds with good biological activity and stability. At present, the demand for green and environmentally friendly pesticides is increasing. If this compound can meet the characteristics of high efficiency, low toxicity and low residue, it will be able to occupy a place in the pesticide market and have a promising future.

As for the field of materials science, with the progress of functional materials research and development, compounds with specific chemical properties are favored. 3 - (phenoxy) -4 - fluoro-benzyl alcohol may participate in the synthesis of special polymers or functional materials, which will contribute to the development of materials science. Market demand will also grow with the progress of materials science.

However, its market prospect is also facing challenges. The complexity of the synthesis process may affect the production cost. If the process cannot be optimized to reduce costs, it may be at a disadvantage in market competition. And it takes time for the market to accept new compounds, and full research and testing are required to prove their practicality and safety in order to successfully promote their application.

What should I pay attention to when storing and transporting 3- (Phenoxy) -4-fluoro-benzyl alcohol?

3- (phenoxy) -4-fluorobenzyl alcohol is an organic compound. When storing and transporting, many aspects must be paid attention to.

First, the temperature and humidity must be appropriate. This compound is mostly sensitive to temperature and humidity, and high temperature or high humidity environment is easy to cause it to deteriorate. Generally speaking, it should be stored in a cool (usually refers to the temperature between 15 and 25 degrees Celsius), dry place, away from heat sources and water sources, to prevent chemical reactions caused by high temperature, or moisture hydrolysis due to high humidity. Second, it needs to be stored away from light. Light often prompts photochemical reactions of compounds, causing their structure to change and performance to be damaged. Therefore, it should be stored in dark containers such as brown bottles and stored in places where light is difficult to reach. Third, it is necessary to ensure that the storage environment is well ventilated. The substance may evaporate harmful gases, and good ventilation can disperse in time to avoid potential safety hazards caused by accumulation, and at the same time reduce the risk of runaway reaction due to high gas concentration. Fourth, classified storage is also crucial. Do not store with strong oxidants, strong acids, strong bases, etc., because it has a certain chemical activity, contact with these substances can easily trigger violent reactions, such as oxidation, acid-base neutralization, etc., endangering storage safety.

As for transportation, the first heavy packaging. Packaging materials must be strong and well sealed to resist vibration, collision and extrusion to prevent leakage. Commonly used, such as glass bottle jacket cushioning materials, and then placed in a sturdy outer packaging box. During transportation, vehicles or transportation tools should be kept stable to avoid severe turbulence and avoid packaging damage. And the transportation environment conditions also need to be controlled, and strive to meet the storage requirements, especially in terms of temperature, humidity and light protection. At the same time, transportation personnel should be familiar with the characteristics of the compound and emergency treatment methods. In case of leakage and other conditions, they can respond quickly and properly to reduce the harm. In short, whether it is storing or transporting 3 - (phenoxy) - 4 - fluorobenzyl alcohol, we must exercise caution and strictly follow relevant norms and requirements to ensure its quality and safety.