Chemical Formula | C6H3BrClF |
Molar Mass | 225.44 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 190 - 192 °C |
Density | 1.807 g/cm³ (approximate) |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Vapor Pressure | Low vapor pressure |
Flash Point | 77 °C (approximate) |
Chemical Formula | C6H3BrClF |
Molar Mass | 211.44 g/mol |
Appearance | Colorless to light yellow liquid |
Boiling Point | 190 - 192 °C |
Melting Point | N/A |
Density | 1.745 g/cm³ |
Solubility In Water | Insoluble |
Flash Point | 78 °C |
Refractive Index | 1.552 - 1.554 |
Vapor Pressure | N/A |
Chemical Formula | C6H3BrClF |
Molecular Weight | 209.44 |
Appearance | Liquid (usually) |
Boiling Point | Approx. 185 - 187 °C |
Density | Approx. 1.80 - 1.90 g/cm³ |
Solubility In Water | Insoluble |
Solubility In Organic Solvents | Soluble in common organic solvents like ethanol, ether |
Vapor Pressure | Low at room temperature |
What is the chemistry of 3-BROMO-4-CHLOROFLUOROBENZENE?
3-Bromo-4-chlorofluorobenzene is one of the organic compounds. Its chemical properties are particularly important and are related to many chemical reactions.
The substitution reaction is discussed first. In this compound, bromine, chlorine and fluorine atoms all have certain activities. Because the fluorine atom is extremely electronegative, the electron cloud density of the benzene ring is reduced, and the electrophilic substitution reaction is more difficult than that of benzene. However, under appropriate conditions, electrophilic substitution can still occur. In case of electrophilic reagents, new groups can be introduced at specific positions on the benzene ring.
Let's talk about the reactivity of its halogen atom. Usually, the activity of bromine atom is slightly higher than that of chlorine atom, and in some nucleophilic substitution reactions, bromine atom For example, when reacting with nucleophiles such as sodium alcohols and amines, bromine atoms can be attacked by nucleophiles first to form new compounds. Among them, the nucleophilicity of nucleophiles and reaction conditions (such as temperature, solvent, etc.) have a great influence on the reaction process and product formation.
Although its fluorine atoms are highly electronegative, they are relatively not easy to be replaced by general nucleophiles. However, under specific conditions, such as high temperature, strong nucleophiles or catalysts, fluorine atoms can also be replaced. Such reactions often require special reaction conditions and catalysts.
In terms of redox reactions, 3-bromo-4-chlorofluorobenzene itself is relatively stable. However, if the benzene ring is connected with an oxidizable or reducible substituent, the corresponding reaction can occur under the action of an appropriate oxidation or reducing agent. For example, if the side chain of the benzene ring has a hydrocarbon group, it can be oxidized to a carboxyl group under the action of a strong oxidizing agent.
And because of its halogen-containing atoms, it can participate in some metal catalytic reactions such as palladium-catalyzed cross-coupling reactions. In such reactions, halogen atoms form intermediates with metal catalysts, which are then coupled with other organic halides or alkenyl and alkynyl compounds to construct more complex organic molecular structures, which is of great significance in the field of organic synthetic chemistry.
In conclusion, 3-bromo-4-chlorofluorobenzene is rich in chemical properties and has broad application prospects in many fields such as organic synthesis and medicinal chemistry. Its diverse reaction characteristics provide many possible ways for the synthesis of various organic compounds.
What are the main uses of 3-BROMO-4-CHLOROFLUOROBENZENE?
3-Bromo-4-chlorofluorobenzene has a wide range of uses. In the field of medicinal chemistry, it is a key intermediate in organic synthesis. It is used as a starting material for the preparation of many drugs. After multi-step reactions, specific functional groups can be introduced to build complex drug molecular structures. For example, some antibacterial drugs use the activity check point of 3-bromo-4-chlorofluorobenzene to achieve precise binding with specific targets of bacteria, so as to exert antibacterial effect.
In the field of materials science, it also plays an important role. It can be used to synthesize new polymer materials, giving materials unique electrical, optical or mechanical properties. Such as the preparation of materials with special photoelectric conversion properties, it shows potential in the field of solar cells and helps to improve the photoelectric conversion efficiency of batteries.
Furthermore, in the field of pesticide chemistry, 3-bromo-4-chlorofluorobenzene is involved in the synthesis of a variety of high-efficiency and low-toxicity pesticides. Through rational molecular design and the use of its structural characteristics, pesticides with high selectivity and strong killing power to specific pests have been developed, while reducing the harm to the environment and non-target organisms, which is in line with the current development trend of green pesticides.
In summary, 3-bromo-4-chlorofluorobenzene is an indispensable and important compound in many fields such as medicine, materials and pesticides, and has made great contributions to promoting the technological progress and development of related industries.
What are 3-BROMO-4-CHLOROFLUOROBENZENE synthesis methods?
There are many ways to synthesize 3-bromo-4-chlorofluorobenzene. One of the common ones is to use fluorobenzene as the starting material. Schilling fluorobenzene and bromine react under the action of appropriate catalysts, such as iron powder or iron tribromide. This reaction needs to be carried out at suitable temperatures and reaction conditions, so that bromine atoms selectively replace hydrogen atoms at specific positions on the benzene ring to generate 4-fluorobromobenzene.
Then, 4-fluorobromobenzene is reacted with chlorine gas under specific conditions. In this process, it is necessary to strictly control the reaction temperature, light conditions and other factors to promote the chlorine atom to replace the hydrogen atom at another specific position on the benzene ring, so as to obtain the target product 3-bromo-4-chlorofluorobenzene.
Second, chlorobenzene can also be used as the starting material. First, chlorobenzene and fluoride react in a specific reaction system to realize the replacement of fluorine atoms with hydrogen atoms on the benzene ring to form fluorochlorobenzene. Subsequently, the generated fluorochlorobenzene reacts with bromine under suitable catalyst and reaction conditions, so that the bromine atom replaces the hydrogen atom at the corresponding position on the benzene ring, and finally 3-bromo-4-chloro
In addition, other suitable starting materials can be selected to synthesize 3-bromo-4-chlorofluorobenzene through a series of carefully designed organic reaction steps, such as nucleophilic substitution, halogenation and other reaction combinations. However, no matter what method is used, it is necessary to precisely control and optimize the reaction conditions of each step, such as temperature, pressure, catalyst type and dosage, in order to improve the yield and purity of the target product.
3-BROMO-4-CHLOROFLUOROBENZENE What are the precautions during storage and transportation?
3-Bromo-4-chlorofluorobenzene is an organic compound. When storing and transporting, many things need to be paid attention to.
First storage conditions. This compound should be placed in a cool, dry and well-ventilated place. Because heat can easily cause its chemical properties to change, or even cause dangerous reactions, it should be kept away from fire and heat sources and avoid direct sunlight. And if it is damp, it may react with water, which will affect the quality, so a dry environment is essential.
Second is the packaging requirement. It needs to be filled with packaging materials with good sealing performance to prevent leakage. Glass bottles or specific plastic containers are commonly used, but it is necessary to ensure that the material of the container does not chemically react with the compound. The name, characteristics and warning label of the compound should be clearly marked on the outside of the package to make it clear to the contact at a glance.
The transportation process should not be underestimated. When transporting, relevant regulations and standards should be followed, and special transportation tools should be equipped. Transportation personnel should be professionally trained and familiar with the characteristics of the compound and emergency disposal methods. During transportation, severe vibration and collision should be prevented to avoid leakage caused by package damage. If leakage occurs during transportation, emergency plans should be activated immediately, surrounding personnel should be evacuated, the leakage area should be isolated, and appropriate disposal measures should be taken according to the characteristics of the compound, such as adsorption with specific adsorbents.
Furthermore, due to its toxicity and irritation, whether it is storage or transportation, operators must take protective measures, such as wearing protective clothing, gloves, goggles, and gas masks, to ensure their own safety.
What is the market price range for 3-BROMO-4-CHLOROFLUOROBENZENE?
The market price range of 3-bromo-4-chlorofluorobenzene is difficult to say with certainty. Its price often changes due to many factors, such as supply and demand, production techniques, raw material prices, market competition, and even changes in the current situation.
Looking at the market situation in the past, if this chemical is blocked trade, the price may vary depending on the quantity. If it is a small amount of demand, such as scientific research, its price is often higher; if it is purchased in large quantities by industry, the unit price may drop slightly due to economies of scale.
In the past few years, its price fluctuated greatly within a specific market range. When the supply of raw materials is sufficient and the production technology is improved, resulting in a large increase in output, the price may decline; conversely, if the raw materials are scarce, or the production is in trouble and the supply is limited, the price will rise easily.
And the market in different regions also has different prices due to logistics costs, local policies, tax differences, etc. In developed industrial places, due to fierce competition and complete facilities, the price may be relatively stable and competitive; and in remote or weak industrial bases, the price may be slightly higher than elsewhere due to transportation and other costs.
If you want to get an accurate price range, you can get close to the current price information by consulting chemical product suppliers, traders, or reviewing recent market survey reports in real time.