Chemical Formula | C7H3BrF N |
Molecular Weight | 200.01 |
Appearance | Solid (Typical) |
Cas Number | 1261947-39-1 |
Solubility In Water | Low (Organic halide - cyanide - fluorobenzene compounds are generally hydrophobic) |
Solubility In Organic Solvents | Good (Soluble in common organic solvents like dichloromethane, chloroform, etc.) |
Name | 3-Bromo-2-cyanofluorobenzene |
Molecular Formula | C7H3BrFN |
Molar Mass | 200.01 g/mol |
Appearance | A colorless to light yellow liquid |
Density | 1.665 g/cm³ (estimated) |
Boiling Point | 223 - 224 °C |
Solubility | Insoluble in water, soluble in organic solvents like dichloromethane |
Flash Point | 99.4 °C |
Purity | Typically available in high purity, e.g., 97%+ |
Chemical Formula | C7H3BrF N |
Molecular Weight | 200.01 |
Appearance | Typically a colorless to light - yellow liquid |
Boiling Point | Approximately in the range of 210 - 220 °C |
Density | Data may vary, but around 1.6 - 1.7 g/cm³ |
Solubility | Soluble in organic solvents like dichloromethane, chloroform |
Purity | Can be produced with high purity, e.g., 95%+ in commercial products |
Stability | Stable under normal storage conditions, but may react with strong oxidizing agents |
What are the main uses of 3-Bromo-2-cyanofluorobenzene?
3-Bromo-2-cyanofluorobenzene is an important intermediate in organic synthesis and has critical uses in many fields.
One is in the field of medicinal chemistry, which has a wide range of uses. Due to the unique reactivity of bromine, cyano and fluorine atoms in the molecule, complex drug molecules can be constructed through various chemical reactions. For example, bromine atoms can participate in nucleophilic substitution reactions, react with reagents containing specific functional groups, and introduce key structural fragments to meet the needs of drugs for specific targets. Cyanide groups can be converted into other functional groups through hydrolysis, reduction and other reactions, expanding the chemical diversity of molecules and providing a structural basis for the development of new drugs. For example, when developing some anti-cancer drugs and anti-infective drugs, 3-bromo-2-cyanofluorobenzene is often used as a starting material to build a core pharmacodynamic structure through multi-step reactions.
Second, it is also indispensable in the field of materials science. With its special structure, it can prepare functional materials with excellent performance. For example, when preparing organic optoelectronic materials, it is introduced into polymer as a structural unit. The presence of fluorine atoms can adjust the electron cloud distribution of the material and affect the optical and electrical properties of the material. Bromine atoms and cyanobenzyl groups can participate in cross-linking reactions to improve the mechanical properties and stability of the material, and are used to manufacture high-performance display materials, Light Emitting Diode materials, etc.
Third, it also plays an important role in the field of pesticide chemistry. As a key intermediate in the synthesis of new pesticides, it can use its structural characteristics to design and synthesize compounds with high insecticidal, bactericidal or herbicidal activities. By modifying its structure and changing the types and positions of substituents, the activity and selectivity of pesticides can be regulated to meet the needs of different crops and pest control.
In summary, 3-bromo-2-cyanofluorobenzene plays an irreplaceable role in the fields of medicine, materials, and pesticides due to its unique structure and reactivity, providing an important material basis for the development of related fields.
What are 3-Bromo-2-cyanofluorobenzene synthesis methods?
The method of preparing 3-bromo-2-cyanofluorobenzene has been followed by many chemists in the past.
First, the fluorobenzene derivative is used as the starting material. Before the appropriate reaction environment, the fluorobenzene derivative is met with the brominating reagent. This brominating reagent, or bromine, is supplemented by iron powder or other suitable catalysts, and by electrophilic substitution, the bromine atom is selectively connected to the benzene ring to obtain the bromine-containing fluorobenzene intermediate. Thereafter, the cyano group is introduced. The cyanide reagent, such as cuprous cyanide, is often used to replace the suitable group on the benzene ring through nucleophilic substitution reaction under specific solvent, temperature and pressure conditions, and finally 3-bromo-2-cyanofluorobenzene is obtained.
Second, it can also start from the aromatic compound with cyanide group. First, the benzene derivative containing cyanide is used to interact with the fluorinated reagent. This fluorinated reagent may be potassium fluoride, etc., with the help of a phase transfer catalyst, the fluorine atom is introduced to obtain the fluorobenzene intermediate containing the cyanide group. Then, the bromination step is carried out, and the bromine atom is connected to the benzene ring by the electrophilic substitution reaction with brominating reagents to achieve the synthesis of 3-bromo-2-cyanofluorobenzene.
Or there may be other synthetic paths, depending on the availability of starting materials, the ease of control of reaction conditions, and the purity requirements of the target product. Each step of the reaction requires fine regulation of reaction temperature, time, material ratio and other conditions, and strives for a smooth reaction and a good product.
What are the physical properties of 3-Bromo-2-cyanofluorobenzene?
3-Bromo-2-cyanofluorobenzene is also an organic compound. Its physical properties are quite important and are described in detail as follows.
Looking at its properties, under normal temperature, 3-bromo-2-cyanofluorobenzene is often colorless to light yellow liquid. This appearance is easy to distinguish intuitively.
When it comes to the melting point, although the relevant exact data may vary depending on the measurement conditions, it is roughly within a certain low temperature range before it begins to condense into a solid state. Its boiling point is also a key physical property. Under specific pressure conditions, when it reaches a certain temperature, the substance changes from a liquid state to a gaseous state. This boiling point temperature can help to separate and purify this compound.
In terms of solubility, 3-bromo-2-cyanofluorobenzene exhibits different degrees of solubility in organic solvents. Generally speaking, it is easily soluble in common organic solvents, such as dichloromethane, chloroform, ether, etc. This property is due to the interaction between its molecular structure and organic solvent molecules, such as van der Waals force, hydrogen bond and other forces. In water, its solubility is relatively poor, due to the difference between the molecular polarity of the compound and the polarity of the water molecule, resulting in weak interaction between the two.
Density is also one of the important physical properties. The density of 3-bromo-2-cyanofluorobenzene may be different from that of water, and this difference is significant when it comes to operations such as liquid-liquid separation.
In addition, the vapor pressure of the compound cannot be ignored. At a certain temperature, it will reach equilibrium with its own steam in a closed container, and the pressure of the steam at this time is the vapor pressure. The magnitude of the vapor pressure is closely related to the temperature. When the temperature increases, the vapor pressure also increases. This property is crucial for considering the evaporation of gases during storage and transportation.
The above physical properties play an important role in the research, production and application of 3-bromo-2-cyanofluorobenzene.
What are the chemical properties of 3-Bromo-2-cyanofluorobenzene?
3-Bromo-2-cyanofluorobenzene is one of the organic compounds. Its chemical properties are of great interest and are described in detail below.
The first discussion on its substitution reaction. Due to the good activity of bromine atoms in molecules, it is often a check point for nucleophilic substitution reactions. In case of nucleophilic reagents, such as alkoxides, amines, etc., bromine atoms can be replaced to form novel compounds. This reaction is crucial in organic synthesis. It can build a diverse organic molecular structure by changing the structure of nucleophilic reagents.
The characteristics of cyanobenzene and cyanobenzene groups. Cyanobenzene groups are highly reactive and can participate in hydrolysis reactions. Under the catalysis of acid or base, the cyanyl group can be converted into carboxyl group, which is an important way to prepare carboxyl-containing compounds. And the cyanyl group can be converted into amino or methylene amino groups through reduction reaction, which greatly enriches the strategy of organic synthesis.
Furthermore, although fluorine atoms do not occupy much space in molecules, their electronegativity is extremely high, which significantly affects the electron cloud distribution of molecules, and then affects the polarity and chemical activity of compounds. The presence of fluorine atoms changes the reactivity of molecules to some electrophilic reagents, and also affects the physical properties of molecules, such as boiling point and solubility.
In addition, the benzene ring structure of 3-bromo-2-cyanofluorobenzene cannot be ignored. The benzene ring is rich in electrons and can undergo electrophilic substitution reactions, such as halogenation, nitrification, sulfonation, etc. And the benzene ring interacts with bromine, cyano and fluorine atoms, causing subtle changes in the activities of each functional group, presenting unique selectivity and reactivity in the reaction.
Overall, the unique properties and interactions of the functional groups of 3-bromo-2-cyanofluorobenzene show broad application prospects in the field of organic synthesis, providing rich possibilities for the creation of various complex organic compounds.
3-Bromo-2-cyanofluorobenzene What are the precautions during storage and transportation?
3-Bromo-2-cyanofluorobenzene is an important raw material for organic synthesis. During storage and transportation, many matters must be paid attention to to to ensure its safety and quality.
When storing, the first choice of environment. It should be placed in a cool and ventilated warehouse, away from fire and heat sources. This substance can easily cause chemical reactions, cause it to deteriorate, and even risk fire and explosion when heated. The temperature of the warehouse should be controlled within a certain range, so as not to affect its stability if the temperature is too high or too low.
Furthermore, it should be stored separately from oxidants, acids, bases, etc., and should not be mixed. Due to its active chemical properties, contact with the above substances is prone to severe chemical reactions and endangers safety. And the storage area should be equipped with suitable materials to contain leaks, so as to prevent accidental leakage and deal with them in time to avoid polluting the environment and causing greater harm.
As for the transportation process, it is also necessary to be treated with caution. Be sure to ensure that the container is well sealed before transportation to prevent leakage. The transportation vehicle should be selected with corresponding qualifications, and equipped with necessary emergency treatment equipment and protective equipment. During transportation, it should be protected from sun exposure, rain and high temperature. When driving, you should drive slowly and avoid violent actions such as sudden braking and sharp turns to prevent package damage.
When loading and unloading, the operator must wear appropriate protective equipment, such as gas masks, gloves, etc., and handle it lightly. It is strictly forbidden to drop and heavy pressure to avoid material leakage due to packaging damage. In the event of a leak, the personnel should be evacuated immediately and the contaminated area should be isolated. Emergency responders should wear protective equipment and take corresponding measures according to the leakage situation, such as absorbing with inert materials such as sand and vermiculite, or neutralizing with suitable chemical reagents.