1 Bromo 2 1 1 Difluoroethyl 4 Fluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-BROMO-2-(1,1-DIFLUOROETHYL)-4-FLUOROBENZENE
Chemical Formula C8H7BrF3
Molecular Weight 239.04
Chemical Formula C8H7BrF3
Molecular Weight 241.04
Stability Stable under normal conditions but may react with strong oxidizing agents
Chemical Formula C8H7BrF3
Molecular Weight 241.04
Appearance Typically a colorless to light - yellow liquid
Boiling Point Data may vary, but around a certain range (needs specific experimental value)
Melting Point Data may vary, but around a certain range (needs specific experimental value)
Density Data may vary, but around a certain range (needs specific experimental value)
Solubility In Water Low solubility in water
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Data may vary, but around a certain range (needs specific experimental value)
Flash Point Data may vary, but around a certain range (needs specific experimental value)
FAQ

What is the main use of 1-BROMO-2- (1,1-DIFLUOROETHYL) -4-FLUOROBENZENE?

1-Bromo-2- (1,1-difluoroethyl) -4-fluorobenzene, this substance has a wide range of uses. In the field of medicinal chemistry, it is often a key intermediate for the creation of new drugs. Due to the unique electronic properties of fluorine atoms, the introduction of organic molecules can significantly change the physical, chemical and biological activities of compounds. With the special arrangement of fluorine and bromine atoms in its structure, chemists can build complex drug molecular structures, enhance the affinity and selectivity of drugs to specific targets, thereby enhancing drug efficacy and reducing side effects.

In the field of materials science, this compound also has important value. Due to its fluorine-containing structure, the material has unique properties such as excellent thermal stability, chemical stability and low surface energy. Therefore, it is often used to develop high-performance polymer materials, such as special plastics, coatings and fibers. Taking special plastics as an example, the incorporation of this compound can improve the weathering resistance, wear resistance and chemical corrosion resistance of plastics, and is widely used in aerospace, electronics and other fields that require strict material properties.

In the field of organic synthetic chemistry, 1-bromo-2 - (1,1-difluoroethyl) -4-fluorobenzene is an important starting material and participates in many organic reactions. Its bromine atom has high activity, and can react with various nucleophiles or organometallic reagents through classical organic reactions such as nucleophilic substitution and coupling reactions to form diverse carbon-carbon and carbon-hetero atomic bonds, providing an effective way for the synthesis of complex organic compounds, assisting organic synthesis chemists to expand the diversity of molecular structures and promoting the development of organic synthesis chemistry.

What are the physical properties of 1-BROMO-2- (1,1-DIFLUOROETHYL) -4-FLUOROBENZENE

1-Bromo-2- (1,1-difluoroethyl) -4-fluorobenzene is an organic compound. Its physical properties are as follows:
First of all, its appearance, under room temperature and pressure, is often colorless to light yellow liquid form, uniform and clear texture, warm luster. Looking at it, there are no obvious impurities or suspended solids, and it is in a pure state.
As for its boiling point, it is about a certain temperature range. Due to the intermolecular forces and structural characteristics, the boiling point has a specific value. In the molecular structure of this compound, the presence of bromine and fluorine atoms changes the intermolecular forces, resulting in a boiling point that is different from ordinary benzene compounds.
Melting point is also an important physical property. After experimental determination, its melting point is in a specific range. When the temperature drops below the melting point, the substance will gradually change from liquid to solid, and the lattice structure will be gradually formed at this time.
In terms of density, it is heavier than water. When it is placed in a container with water, it can be seen that it sinks to the bottom of the water. This is due to the type and number of atoms in the molecule. The atomic mass and spatial arrangement work together to create such density characteristics.
Solubility cannot be ignored. In organic solvents such as ethanol and ether, 1-bromo-2 - (1,1-difluoroethyl) -4-fluorobenzene exhibits good solubility and can be miscible with organic solvents to form a uniform solution. However, in water, its solubility is very small, due to the hydrophobicity of the compound, and the polarity of the molecule is quite different from that of the water molecule, making it difficult for the two to dissolve.
In addition, the volatility of the compound is relatively moderate, and it will evaporate slowly in the air. The thermal motion of the molecule and the energy exchange with the surrounding environment allow some molecules to obtain enough energy to leave the liquid phase and enter the gas phase. Although this process is relatively slow, it is also an important manifestation of its physical properties.

What are the chemical properties of 1-BROMO-2- (1,1-DIFLUOROETHYL) -4-FLUOROBENZENE?

1-Bromo-2- (1,1-difluoroethyl) -4-fluorobenzene, this is an organic compound. Its chemical properties are unique, and for the purpose of investigation, it can be carefully observed from the following numbers.

First of all, its physical properties are described. It may be liquid at room temperature, with a specific boiling point and melting point. Because it contains halogen atoms such as bromine and fluorine, the molecular polarity is different from ordinary hydrocarbons, resulting in its unique solubility. In organic solvents, it may have good solubility, but in water, the solubility may not be good. This is due to the high electronegativity of halogen atoms, which affects the overall polarity of molecules.

Once again discuss its chemical properties. First, halogen atoms are active and can undergo substitution reactions. The bromine atom can be replaced by a nucleophilic reagent. If it encounters a hydroxyl negative ion, it may form a corresponding phenolic derivative; if it reacts with an amino negative ion, it may obtain a nitrogen-containing derivative. This all stems from the generality of the nucleophilic substitution reaction of halogenated hydrocarbons. The bromine atom acts as a leaving group, and the nucleophilic reagent attacks the carbon atom it connects to to form a new chemical bond.

Second, although the fluorine atom is not as easy to leave as the bromine atom, its electronegativity is extremely high, which can affect the electron cloud density of the benzene ring. The activity of the electrophilic substitution reaction on the benzene ring may be influenced by it. In the electrophilic substitution reaction of the benzene ring, the fluorine atom reduces the electron cloud density of the The electron cloud density of the ortho and para-position is relatively high, and electrophilic reagents may more easily attack these two positions.

Third, the 1,1-difluoroethyl group in the molecule, difluoromethyl also affects the molecular properties. Because of its electron absorption, or enhance molecular polarity, and in specific reactions, or form a unique reaction check point. In case of strong reducing agent, difluoromethyl may be reduced and structural transformation occurs.

In summary, 1-bromo-2- (1,1-difluoroethyl) -4-fluorobenzene is rich in chemical properties, and the interaction between halogen atoms and fluorine-containing groups makes it have potential application value in the field of organic synthesis. Organic compounds with complex structures can be constructed through various reaction paths.

What are the synthesis methods of 1-BROMO-2- (1,1-DIFLUOROETHYL) -4-FLUOROBENZENE

There are many different ways to synthesize 1-bromo-2- (1,1-difluoroethyl) -4-fluorobenzene.

First, it can be started from fluorobenzene derivatives. First, take a suitable fluorobenzene and make it react with a specific halogenated reagent, such as a halogen containing bromine and difluoroethyl structure, under the action of a suitable catalyst. This catalyst, or a metal salt, can promote the nucleophilic substitution reaction. The reaction environment needs to be precisely controlled, and the choice of temperature and solvent is the key. Polar organic solvents are preferred, such as dimethylformamide (DMF), because they can dissolve the reactants and help the reaction process. The temperature varies depending on the activity of the reactants. Usually under moderate heating conditions, the reaction can take place effectively, so that the halogen atom binds to a specific position on the benzene ring to obtain the target product.

Second, it can also be conceived from another angle. First build the basic structure of the benzene ring, and then gradually introduce fluorine, bromine, and difluoroethyl groups. For example, first prepare benzene derivatives, and use organic synthesis methods, such as electrophilic substitution reaction, to introduce fluorine atoms and bromine atoms in turn. After that, by reacting with difluoroethylation reagents, the connection of difluoroethyl groups is realized. In this process, the rational use of protective groups is very important to prevent other groups from reacting unnecessarily. When the reaction is successfully completed in each step, and after appropriate separation and purification operations, such as column chromatography, recrystallization, etc., pure 1-bromo-2- (1,1-difluoroethyl) -4-fluorobenzene can be obtained.

Furthermore, reference can be made to the synthesis strategy of similar structural compounds in the literature, and the reaction conditions and reagents can be adjusted appropriately according to the structural characteristics of the target. The method of organic synthesis is changeable and multi-terminal, and it needs to be flexibly selected according to the actual situation to achieve the purpose of efficient synthesis.

1-BROMO-2- (1,1-DIFLUOROETHYL) -4-FLUOROBENZENE What are the precautions in storage and transportation?

1-Bromo-2- (1,1-difluoroethyl) -4-fluorobenzene This substance requires attention to many matters during storage and transportation.

The first thing to bear the brunt is the control of storage temperature. Due to its nature or temperature, it should be placed in a cool place to avoid exposure to the sun and high temperature to prevent its deterioration or danger. Generally speaking, under normal temperature, it needs to be maintained in a specific range, and it must not be overheated to avoid internal structural changes and changes in its chemical activity.

Furthermore, humidity cannot be ignored. This substance may be afraid of moisture. If the ambient humidity is too high, the water vapor may react chemically with it, so it should be stored in a dry place, and a desiccant can be prepared next to it to ensure its dry environment.

When transporting, the packaging must be solid and reliable. Appropriate packaging materials need to be selected to prevent damage to the packaging due to vibration and collision. Because of its certain chemical properties, once it leaks or pollutes the environment, it may even endanger the safety of surrounding personnel.

In addition, the conditions of the transportation vehicle are also exquisite. The environment inside the vehicle should be clean and free of other substances that can react with it. And during transportation, it is necessary to closely monitor environmental factors such as temperature and humidity to ensure a stable transportation environment.

It should also be noted that this substance should be placed and transported separately from oxidizing, corrosive and other substances of different properties to prevent interaction and accidents. Operators should be familiar with its characteristics, wear protective equipment, and operate according to standard procedures, so as to ensure the safety of storage and transportation.