Bromo Fluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
Bromo fluorobenzene
Chemical Formula C6H4BrF
Molar Mass 175.00 g/mol
Appearance Colorless to pale yellow liquid
Boiling Point 150 - 152 °C
Melting Point -27 °C
Density 1.57 g/cm³
Solubility In Water Insoluble
Vapor Pressure 1.33 kPa at 39.4 °C
Flash Point 47 °C
Refractive Index 1.545 - 1.547
Chemical Formula C6H4BrF
Molar Mass 175.00 g/mol
Appearance Colorless to light - yellow liquid
Boiling Point 154 - 156 °C
Melting Point −27 °C
Density 1.57 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point 53 °C
Vapor Pressure Low vapor pressure at room temperature
Odor Characteristic aromatic odor
Name Bromo fluorobenzene
Molecular Formula C6H4BrF
Molar Mass 175.00 g/mol
Appearance Colorless to light yellow liquid
Density 1.57 g/cm³
Boiling Point 157 - 159 °C
Melting Point -32 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble
Flash Point 47 °C
Vapor Pressure 1.25 mmHg at 25 °C
Refractive Index 1.542
FAQ

What are the main uses of Bromo fluorobenzene?

Bromofluorobenzene is one of the organic compounds. It has a wide range of uses and is very useful in the field of organic synthesis.

First, it can be used as a raw material for pharmaceutical synthesis. In the process of drug development, bromofluorobenzene can be used as a key intermediate. Because of the presence of bromine and fluorine atoms in its molecular structure, it is endowed with unique chemical activities and can participate in various chemical reactions to build complex drug molecular structures. For example, when synthesizing some antibacterial drugs and nervous system drugs, bromofluorobenzene is often an indispensable starting material. Through ingenious chemical reactions, drug molecules with specific pharmacological activities are gradually built.

Second, it also plays an important role in the synthesis of pesticides. The research and development of pesticides aims to effectively control pests and diseases and ensure a bumper crop harvest. Bromofluorobenzene can be used as an important component in the synthesis of high-efficiency and low-toxicity pesticides due to its special chemical properties. After a series of reactions, pesticide products with high selectivity and strong lethality to specific pests or bacteria can be prepared, and can meet the requirements of modern agriculture for environmentally friendly pesticides and low residues.

Third, it is also applied in the field of materials science. The preparation of some high-performance materials requires the introduction of special functional groups to improve material properties. The bromine and fluorine atoms carried by bromofluorobenzene can participate in the material polymerization reaction, giving the material excellent characteristics such as chemical resistance and thermal stability. For example, in the synthesis of some special plastics and coatings, bromofluorobenzene can be used as a modifier to improve material quality and expand its application range.

What are the physical properties of Bromo fluorobenzene?

Bromofluorobenzene is one of the organic compounds. It has a number of physical properties and is quite impressive.

First of all, its appearance, bromofluorobenzene is often colorless to light yellow transparent liquid, clear and with a certain luster, it seems to have a smart state. Its smell is unique, but it is not pungent and intolerable, but has a specific aromatic smell, which gives people a different sense of smell.

When it comes to boiling point, the boiling point of bromofluorobenzene is within a certain range. Due to the intermolecular force, its boiling point is moderate, neither extremely high nor extremely low. This property makes it exhibit specific behaviors during operations such as heating or distillation. When heated to its boiling point, bromofluorobenzene gradually changes from liquid to gaseous state. This process is smooth and follows the laws of physics. In chemical operations or experimental investigations, the characteristics of boiling point provide an important basis for separation and purification.

In terms of melting point, bromofluorobenzene also has its inherent value. When the ambient temperature drops below the melting point, the substance solidifies from liquid to solid state. Its solid state or regular crystal structure is determined by the molecular arrangement. The existence of the melting point makes bromofluorobenzene exhibit different physical states at different temperatures, which also affects its storage and transportation.

In terms of density, bromofluorobenzene is different from water. Its density is greater than that of water, so if mixed with water, it will sink to the bottom of the water. This density characteristic is of great significance when it involves operations such as liquid-liquid separation. The difference in density can be used to separate bromofluorobenzene from water or other liquids of different densities by simple physical methods.

Solubility is also a key physical property. Bromofluorobenzene is insoluble in water, because water is a polar molecule, while the molecular polarity of bromofluorobenzene is relatively weak. According to the principle of "similar miscibility", the two are difficult to miscible. However, it is soluble in many organic solvents, such as ethanol, ether, etc. This solubility characteristic lays the foundation for its application in organic synthesis and other fields. It can be used as a reaction medium or participate in various organic reactions.

In summary, the physical properties of bromofluorobenzene are diverse and interrelated. They play an important role in the research of organic chemistry and the application of industrial production, providing a material basis and basis for the development of many fields.

Bromo fluorobenzene chemical properties

Bromofluorobenzene is an organic compound, and its molecules contain bromine, fluorine and benzene rings. The chemical properties of this compound are unique due to the presence of bromine and fluorine atoms.

The benzene ring is aromatic, and its electron cloud distribution is uniform and stable. However, the introduction of bromine and fluorine atoms changes the distribution of molecular electron clouds. Bromine atoms have a large atomic radius and lone pairs of electrons, and fluorine atoms are extremely electronegative.

In terms of reactivity, bromofluorobenzene can participate in nucleophilic substitution reactions. Under appropriate conditions, bromine atoms can be replaced by nucleophilic reagents. Because the bromine atom is connected to the benzene ring, its C-Br bond has a certain polarity, and the nucleophilic reagent can attack the carbon atom connected to the bromine, causing the bromine to leave and form new compounds.

Although the fluorine atom is highly electronegative, it is more difficult for it to participate in the nucleophilic substitution reaction than bromine, because the C-F bond energy is higher. However, under special reagents and conditions, the fluorine atom may also be replaced.

In addition, bromofluorobenzene can participate in the electrophilic substitution reaction. The electron cloud of the benzene ring can attract electrophilic reagents. Although the bromine and fluorine atoms are electron-absorbing groups, the electron cloud density of the benzene ring is reduced, and the Electrophilic reagents often attack specific positions on the benzene ring and are affected by the localization effect of bromine and fluorine atoms.

The localization effect of bromine and fluorine atoms is different. Bromine is an ortho-and para-localization group, and fluorine also has a similar localization tendency. Therefore, electrophilic reagents often attack carbon atoms in the ortho-or para-position of bromine and fluorine atoms on the benzene ring to form corresponding substitutions.

In the redox reaction, if bromofluorobenzene encounters strong oxidants, the benzene ring may be oxidized, or the valence state of bromine and fluorine atoms may change. In the case of strong reducing agents, the C-Br bond or C-F bond may be reduced and broken.

In summary, the interaction of bromofluorobenzene bromide, fluorine atom and benzene ring has unique chemical properties and is widely used in the field of organic synthesis. Organic compounds with diverse structures can be prepared through various reactions.

What are the synthesis methods of Bromo fluorobenzene

The method of preparing bromofluorobenzene is often obtained by the reaction of halogenation with benzene as the starting material. One method is: the benzene, the brominating agent and the fluorinating agent are co-placed in a special container, and an appropriate catalyst is added to control the temperature and pressure of the reaction. For example, using iron bromide as the catalyst, benzene and bromine are first combined to obtain bromobenzene; then bromobenzene and the fluorinating agent, such as potassium fluoride, are combined in a specific organic solvent, such as dimethyl sulfoxide, and heated to promote its substitution. Bromofluorobenzene can be obtained.

Another method, or a special process of halogenation of aromatic hydrocarbons, can be used to make benzene in the same reaction system, and bromine and fluorine atoms are introduced at the However, it is necessary to choose the appropriate halogenation reagent and reaction conditions to control the position and degree of halogenation. For example, with a specific compound halogenating agent, in the presence of a phase transfer catalyst, the halogenation reaction of benzene is carried out, and the reaction environment is precisely regulated to obtain the target bromofluorobenzene product.

In addition, there are also people who use other organic compounds as starting materials to synthesize bromofluorobenzene through multi-step reactions. However, such methods are often complicated and costly, and are not commonly used in industry. In actual preparation, it is necessary to weigh the cost of raw materials, the difficulty of reaction, the purity and yield of the product, and many other factors, and choose the optimal synthesis path to achieve the purpose of efficient preparation of bromofluorobenzene.

Bromo fluorobenzene in storage and transportation

Bromofluorobenzene, during storage and transportation, all kinds of precautions need to be carefully reviewed.

The first word storage, this material is special, should be placed in a cool and well ventilated place. Because it may be sensitive to temperature and humidity, the control of temperature and humidity is crucial. If the temperature is too high, it may cause its chemical properties to be unstable, resulting in danger; if the humidity is too high, it may react with water vapor and damage its quality. And it must be kept away from fire and heat sources, because bromofluorobenzene is flammable or chemically active, in case of open flames and hot topics, it may lead to fire and explosion.

Furthermore, when storing, it should be stored separately from oxidants, acids, alkalis, etc., and must not be mixed. Due to its chemical properties, it is easy to react chemically with such substances, or cause violent reactions, endangering storage safety.

As for transportation, bromofluorobenzene must be properly packaged to ensure that the packaging is not damaged or leaked during the bumpy transportation. Transportation vehicles are also selected as appropriate and equipped with corresponding safety protection facilities. When driving, drivers should drive carefully to avoid densely populated areas and high-temperature road sections to prevent accidents and affect public safety. Transportation personnel should also be familiar with the characteristics of bromofluorobenzene and emergency treatment methods. In case of leakage and other emergencies, they can be disposed of quickly and properly to reduce the harm. And during transportation, relevant regulations and standards should be strictly followed to ensure legal compliance and safety.