2 Chloro 3 6 Difluorobenzyl Bromide
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Chloro-3,6-difluorobenzyl bromide
Chemical Formula C7H4BrClF2
Molecular Weight 257.46
Appearance Typically a colorless to light - yellow liquid
Boiling Point Data may vary, but generally in a certain range related to its molecular structure
Melting Point Specific value based on its crystal lattice characteristics
Density Determined by mass - volume relationship
Solubility Solubility in organic solvents like dichloromethane, less soluble in water
Vapor Pressure Related to its volatility at different temperatures
Flash Point Important for fire - safety considerations
Reactivity Reactive towards nucleophiles due to the presence of bromine and chlorine
Name 2-Chloro-3,6-difluorobenzyl bromide
Chemical Formula C7H4BrClF2
Molecular Weight 241.46
Appearance Liquid (usually)
Boiling Point Data varies, typically in range of organic halogenated compounds
Solubility Soluble in organic solvents like dichloromethane, less in water
Vapor Pressure Low, typical for halogenated aromatic liquids
FAQ

What are the chemical properties of 2-Chloro-3,6-difluorobenzyl bromide?

2-Chloro-3,6-difluorobenzyl bromide, this is an organic compound. Its chemical properties are unique and need to be investigated in detail.

Let's talk about its activity first, because there are bromine atoms and chlorine atoms in the molecule, both of which are halogen atoms. Halogen atoms make this compound highly reactive. Both bromine and chlorine atoms have certain electronegativity, which attracts electrons and makes the carbon atoms connected to them partially positively charged, so they are vulnerable to attack by nucleophiles.

Nucleophilic substitution reaction is one of its important chemical properties. Nucleophiles, such as hydroxide ions, alkoxide ions, etc., are prone to attack benzyl carbons, and bromine atoms or chlorine atoms will leave as leaving groups, thereby forming new compounds. For example, when co-heated with sodium hydroxide solution, bromine atoms or chlorine atoms can be substituted by hydroxyl groups to form corresponding alcohol compounds.

Furthermore, because fluorine atoms are connected to the benzene ring, fluorine atoms are extremely electronegative, which will affect the distribution of electron clouds in the benzene ring. It will reduce the electron cloud density of the benzene ring, thereby reducing the activity of the electrophilic substitution reaction of the benzene ring. However, for nucleophilic substitution reactions, the electron-withdrawing effect of fluorine atoms will change the stability of benzyl carbon positive ion intermediates and have an effect on the reaction process.

At the same time, the compound may also undergo elimination reaction under appropriate conditions. If there is a strong base and certain stereochemical conditions are met, the halogen atom and hydrogen atom on the adjacent carbon atom can be removed to form a carbon-carbon double bond, forming an unsaturated compound.

In addition, its chemical properties are also affected by reaction conditions such as temperature and solvent. In polar solvents, the rate of nucleophilic substitution may be accelerated, because polar solvents help stabilize the reaction intermediate and transition state. When the temperature increases, the reaction rate will usually also be accelerated, because more molecules can obtain enough energy to cross the reaction energy barrier. The presence of halogen and fluorine atoms in the molecular structure of 2-chloro-3,6-difluorobenzyl bromide exhibits diverse chemical properties, and can participate in many reactions as an important intermediate in the field of organic synthesis. Through rational selection of reaction conditions, effective regulation of its reaction direction and products can be achieved.

What are the main uses of 2-Chloro-3,6-difluorobenzyl bromide

2-Chloro-3,6-difluorobenzyl bromide, this substance has a wide range of uses. In the field of medicine, it is often used as a key intermediate to help create various kinds of specific drugs. In the synthesis of Gain drugs, its unique chemical structure can participate in many key reactions. After clever transformation, a molecular structure with specific pharmacological activities is constructed, which contributes to the cause of human health.

In the pesticide industry, it also plays an important role. It can derive high-efficiency pesticides, fungicides and other pesticide products. With its chemical properties, it can effectively kill pests and inhibit the growth of pathogens. It contributes significantly to ensuring the robust growth of crops and improving food production, and protects the prosperity of agriculture.

In the field of materials science, 2-chloro-3,6-difluorobenzyl bromide is also useful. Or it can be used to prepare new materials with special properties, such as improving the stability and solubility of materials, injecting vitality into the progress of materials science, promoting the emergence of many new materials, and meeting the special needs of materials in different fields.

This compound has important applications in many fields. It is an indispensable key substance in the chemical industry and has a profound impact on the development of various industries.

What is the synthesis method of 2-Chloro-3,6-difluorobenzyl bromide

To prepare 2-chloro-3,6-difluorobenzyl bromide, the following ancient method can be used.

Take 2-chloro-3,6-difluorotoluene as the starting material. In a clean reactor, add an appropriate amount of initiator, such as azobisisobutyronitrile, which can generate free radicals at a suitable temperature to initiate the reaction. Then seal the reactor and pass nitrogen to remove the air in it to prevent side reactions from occurring. Then, slowly add an appropriate amount of bromine, and at the same time, control the reaction temperature within a certain range, generally about 100-120 ° C. At this temperature, bromine under the action of an initiator generates bromine free radicals, which attack the benzyl position of 2-chloro-3,6-difluorotoluene. After the radical substitution reaction, 2-chloro-3,6-difluorobenzyl bromide is obtained.

During the reaction, gas chromatography and other means are required to monitor the reaction process in real time to show the degree of reaction. After the reaction is completed, the reaction mixture is cooled to room temperature. Then, an appropriate amount of saturated sodium sulfite solution is added to remove unreacted bromine. Separate the solution, take the organic phase, and wash it with water and sodium bicarbonate solution in turn to remove impurities. Then dry the organic phase with anhydrous sodium sulfate, filter out the desiccant, and then evaporate under reduced pressure to collect fractions with suitable boiling points to obtain pure 2-chloro-3,6-difluorobenzyl bromide products. In this process, the operation needs to be fine, and the conditions of each step need to be strictly controlled to obtain the ideal yield and purity.

What are the precautions for 2-Chloro-3,6-difluorobenzyl bromide in storage and transportation?

2-Chloro-3,6-difluorobenzyl bromide is an important intermediate in organic synthesis. During storage and transportation, many important items must not be ignored.

Bear the brunt, the temperature and humidity of storage are of great significance. This material should be stored in a cool, dry place, away from heat sources and fires. If the temperature is too high, it may cause it to decompose and deteriorate; if the humidity is too high, it can also cause many reactions and damage its quality. Therefore, in the warehouse, the control of temperature and humidity must be accurate.

In addition, it is toxic and corrosive to a certain extent. When storing, the packaging must be tight to prevent leakage. The packaging material is selected to be corrosion-resistant and well-sealed. Once it leaks, it not only endangers the environment, but also poses a threat to the safety of personnel.

When transporting, there are also many precautions. It is necessary to follow relevant regulations and standards and choose the appropriate means of transportation. Do not mix with oxidizing agents, alkalis, etc., because of their active chemical properties, contact with them, or react violently, resulting in dangerous accidents.

During transportation, escort personnel must always pay attention to the condition of the goods to ensure that the packaging is not damaged. In case of abnormalities, they should be properly disposed of in time. During loading and unloading, it is also necessary to be careful and handle with care to avoid collisions and drops to prevent packaging damage.

In short, when storing and transporting 2-chloro-3,6-difluorobenzyl bromide, the control of temperature and humidity, the solidification of packaging, the rules of transportation, and the caution of operation are all crucial.

What is the market price range for 2-Chloro-3,6-difluorobenzyl bromide?

In today's world, business conditions are unpredictable, and it is not easy to understand the market price range of 2-chloro-3,6-difluorobenzyl bromide. However, you can follow the business conditions of the past to get a general idea.

In the past, the price of these chemical materials often depended on factors such as supply and demand, difficulty in production, and the price of raw materials. If there are many people who need it, and the production is difficult, the price of raw materials will rise; on the contrary, if the demand is low, the production capacity is abundant, and the price of raw materials is cheap, the price may drop.

Looking at the market in the past, the price of 2-chloro-3,6-difluorobenzyl bromide may vary from time to time. When supply and demand are in balance, its price may be stable within a certain range; if there is a market fluctuation, such as a sudden increase in demand, and the supply does not match the corresponding, the price will rise; or if the production capacity expands suddenly and the demand does not grow, the price will drop.

Generally speaking, its market price per kilogram may range from a few hundred to several thousand yuan. However, this is only a rough estimate and cannot be specified. Between market changes, prices vary from place to place, and the time of transaction is different, which can make prices different. Or due to the enactment of new regulations, environmental protection has become stricter, resulting in changes in production costs, and prices have also changed accordingly. Therefore, in order to know the exact market price range of 2-chloro-3,6-difluorobenzyl bromide, it is necessary to observe the real-time market conditions of the chemical industry, consult the industry merchants, brokers, or refer to professional market information platforms to obtain accurate figures.