4 Chloro 2 Fluorobenzyl Chlorid
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
4-CHLORO-2-FLUOROBENZYL CHLORID
Chemical Formula C7H5Cl2F
Molar Mass 181.02 g/mol
Appearance Colorless to light - yellow liquid
Boiling Point Approximately 200 - 210 °C
Density Around 1.35 - 1.45 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, acetone, dichloromethane
Flash Point Caution: Flammable, flash point likely in the range of 70 - 90 °C
Odor Pungent, characteristic aromatic - chlorinated odor
Chemical Formula C7H5Cl2F
Molar Mass 181.02 g/mol
Appearance Liquid
Boiling Point 202 - 204 °C
Density 1.39 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents
Vapor Pressure Low
Flash Point 87 °C
Odor Pungent
FAQ

What are the main uses of 4-CHLORO-2-FLUOROBENZYL CHLORID?

4-Chloro-2-fluorobenzyl chloride has a wide range of uses. In the field of organic synthesis, it is an important intermediate. The chlorine atom and benzyl structure in the molecule give it unique reactivity.

First, it is often used to construct complex organic compounds. It can be combined with many nucleophilic reagents by nucleophilic substitution reaction. For example, when reacted with alcohols, corresponding ether compounds can be generated. In drug synthesis, it is helpful to introduce specific functional groups to adjust the properties of drug molecules, such as solubility and activity.

Second, it is also used in materials science. It can be used as a monomer to participate in polymerization reactions to prepare polymer materials with special properties. The introduction of fluorine atoms can improve the chemical resistance and thermal stability of the material.

Third, in the field of pesticides, 4-chloro-2-fluorobenzyl chloride can be used as a key raw material for the synthesis of new pesticides. After a series of reactions, pesticide products with high insecticidal and bactericidal activities are synthesized, which is helpful for pest control in agricultural production.

Fourth, in the process of pharmaceutical research and development, this is used as a starting material to construct a molecular skeleton with biological activity through multi-step reactions. After modification and optimization, it is expected to develop innovative drugs for treating specific diseases. In conclusion, 4-chloro-2-fluorobenzyl chloride plays an indispensable role in many fields, such as organic synthesis, materials science, pesticides, and medicine, due to its unique chemical structure. It is of great significance to promote the development of various fields.

4-CHLORO-2-FLUOROBENZYL the physical properties of CHLORID

4-Chloro-2-fluorobenzyl chloride, this is an organic compound. Looking at its physical properties, it is mostly a colorless to light yellow liquid under normal circumstances, emitting a pungent smell, just like the ancient books say "its gas punches the nose".

When it comes to boiling point, it is about a specific range, but the exact value varies according to the experimental conditions, just like the physical properties recorded in ancient books, which vary from time to place. Its density is heavier than water, so when poured into water, it will sink to the bottom. This is the image of "heavier than water, sinking in the abyss". < Br >
In terms of solubility, it can be well dissolved in organic solvents such as ethanol and ether, just like fish entering water and blending freely; however, the solubility of water is not good, just like oil and water, difficult to mix.

Volatility, with a certain degree of volatility, gradually evaporates in the air, such as light smoke, it needs to be properly sealed and stored to prevent escape, "airtight for storage, to prevent its escape".

In addition, 4-chloro-2-fluorobenzyl chloride is flammable, and in case of open flames, hot topics, or combustion, or even explosions, it is like a hidden scourge, which cannot be prevented. When using it, when away from the source of fire, operate with caution to ensure safety, "stay away from open flames, and operate with caution to prevent accidents".

4-CHLORO-2-FLUOROBENZYL CHLORID is chemically stable?

4-Chloro-2-fluorobenzyl chloride, this is an organic compound. The stability of its chemical properties needs to be viewed from multiple perspectives.

In terms of its structure, among benzyl chlorides, the chloromethyl group connected to the benzene ring is chemically active. The benzyl carbocation is stabilized by the conjugation effect of the benzene ring, so that the chlorine atoms are easily left in the form of chloride ions, which can lead to nucleophilic substitution reactions. Under many reaction conditions, this property often makes these compounds exhibit high reactivity.

In 4-chloro-2-fluorobenzyl chloride, the chlorine and fluorine atoms on the benzene ring also affect its chemical properties. Fluorine atoms have strong electronegativity, which can absorb electrons by induction effect, reduce the electron cloud density of the benzene ring, and then affect the electrophilic substitution reactivity on the benzene ring; although chlorine atoms also have electron-absorbing induction effect, their electron-giving conjugation effect will also play a role in some cases. The combined effect of the two causes the reaction activity and reaction check point of the compound to show unique characteristics.

Under normal storage conditions, if placed in a cool, dry and dark place, avoid contact with strong oxidants, strong bases and other active substances, its stability is good. However, once encountering suitable reaction conditions, such as the presence of nucleophiles, the chlorine atom at the benzyl position is highly susceptible to attack by nucleophiles, and nucleophilic substitution occurs, generating corresponding substitution products. From this point of view, the chemical properties of 4-chloro-2-fluorobenzyl chloride are not absolutely stable, and under certain conditions, various chemical reactions are prone to occur, showing high reactivity.

What is the production method of 4-CHLORO-2-FLUOROBENZYL CHLORID?

4-Chloro-2-fluorobenzyl chloride is also an organic compound. Its preparation method is mostly based on the path of chemical synthesis in the past.

One method is also to use 4-chloro-2-fluorotoluene as the starting material. First, a specific halogenating agent, such as chlorine, is used under suitable reaction conditions, such as light or in the presence of an initiator. Chlorination reaction at the benzyl position is carried out under suitable reaction conditions, such as light or in the presence of an initiator. The action of light can make the chlorine molecule split into a chlorine radical, which replaces the hydrogen atom at the benzyl position of 4-chloro-2-fluorotoluene to generate 4-chloro-2-fluorobenzyl chloride. However, in this process, the control of the reaction conditions is extremely important. If the temperature is too high, side reactions will occur frequently, or the formation of polychlorinated products will be caused; if the temperature is too low, the reaction rate will be slow and take a long time.

There is another way, which can be started from 4-chloro-2-fluorobenzoic acid. First reduce it to 4-chloro-2-fluorobenzyl alcohol, and the reducing agent used, such as lithium aluminum hydride, needs to be carefully operated under anhydrous and low temperature conditions, because its activity is quite high. After obtaining 4-chloro-2-fluorobenzyl alcohol, it reacts with chlorinated reagents such as thionyl chloride. This step is relatively mild. The thionyl chloride interacts with the alcohol hydroxyl group to obtain 4-chloro-2-fluorobenzyl chloride through substitution reaction. The by-product is a gas, which is easy to separate and is conducive to improving the purity of the product.

When preparing this compound, it is necessary to pay attention to the precise regulation of the reaction conditions, the purity of the raw materials, and the separation and purification of the product to obtain high-purity 4-chloro-2-fluorobenzyl chloride.

What are the precautions for 4-CHLORO-2-FLUOROBENZYL CHLORID in storage and transportation?

4-Chloro-2-fluorobenzyl chloride, this is a chemical substance. When storing and transporting, many matters need to be paid attention to.

First, the storage place must be dry and cool. Because it is afraid of moisture and heat, moisture can easily cause it to deteriorate, and high temperature may cause its chemical reaction, it is advisable to choose a well-ventilated place with moderate temperature and away from heat and fire sources to avoid the risk of fire and explosion.

Second, it is toxic and corrosive to a certain extent. When storing, the packaging must be tightly sealed to prevent leakage. The packaging materials used should be able to withstand its corrosion to ensure safety. If damage to the packaging is detected during storage, immediate measures should be taken to prevent leakage from spreading.

Furthermore, when transporting, follow relevant regulations and standards. Transportation vehicles need to be equipped with corresponding protective equipment and emergency response tools, and escort personnel should also be familiar with the characteristics of this material and emergency treatment methods. During transportation, avoid bumps and collisions to prevent damage to the packaging.

In addition, isolation from other substances is also key. Do not mix with oxidants, alkalis, etc., because of their violent reactions with them, endangering safety.

In short, the storage and transportation of 4-chloro-2-fluorobenzyl chloride is related to safety, and it is necessary to be careful and not negligent to ensure the safety of personnel and the environment.