2 Bromo 4 Chloro 1 Fluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Bromo-4-chloro-1-fluorobenzene
Chemical Formula C6H3BrClF
Molecular Weight 211.44
Appearance Colorless to light yellow liquid
Boiling Point Approximately 195 - 200 °C
Density Data may vary, around 1.7 - 1.8 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point Data may vary, but potentially flammable
Vapor Pressure Low at room temperature
Odor Characteristic, pungent organic odor
Chemical Formula C6H3BrClF
Appearance Colorless to light yellow liquid
Boiling Point 185 - 187 °C
Density 1.734 g/mL at 25 °C
Flash Point 74 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Odor Characteristic aromatic odor
Chemical Formula C6H3BrClF
Molar Mass 211.44 g/mol
Appearance Colorless to light yellow liquid
Boiling Point Approx. 175 - 180 °C
Density Approx. 1.72 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point Approx. 68 °C
Refractive Index Approx. 1.555
FAQ

What are the chemical properties of 2-Bromo-4-chloro-1-fluorobenzene?

2-Bromo-4-chloro-1-fluorobenzene is one of the organohalogenated aromatic hydrocarbons. Its chemical properties are quite interesting, with the characteristics of both aromatics and halogenated hydrocarbons.

As far as the electrophilic substitution reaction is concerned, the benzene ring is electron-rich, so it is easy to be attacked by electrophilic reagents. However, the existence of halogen atoms has a great impact on the electron cloud density of the benzene ring. Fluorine, chlorine, and bromine trihalogen atoms all have electron-absorbing effects, causing the electron cloud density of the benzene ring to drop, and the reactivity is lower than that of benzene. However, their localization effects Fluorine, chlorine, and bromine are all ortho-para-sites. During the electrophilic substitution reaction, the newly introduced group more than enters the ortho-site or para-site of the halogen atom.

In the nucleophilic substitution reaction, the halogen atom can be replaced by the nucleophilic reagent. However, due to the conjugation of the benzene ring, the C-X bond has some double bond properties, and the activity of the halogen atom is lower than that of the halogenated alkane. Generally speaking, the reaction can be smooth under specific conditions. If the halogen atom is replaced with the nucleophilic reagent at high temperature, strong base or in the presence of a catalyst, the halogen at

In addition, 2-bromo-4-chloro-1-fluorobenzene can participate in metal-catalyzed reactions, such as palladium-catalyzed coupling reactions. In such reactions, it can be coupled with compounds containing active chemical bonds to form carbon-carbon or carbon-heteroatomic bonds, which are widely used in the field of organic synthesis. And because it contains a variety of halogen atoms, it can selectively activate and react, providing a variety of strategies for the synthesis of complex organic molecules. The chemical properties of this compound are of great importance to organic synthesis chemists, which can be used to create novel organic materials, drugs and other compounds.

What are the main uses of 2-Bromo-4-chloro-1-fluorobenzene?

2-Bromo-4-chloro-1-fluorobenzene is also an organic compound. It has a wide range of uses and is an important intermediate in the field of pharmaceutical synthesis. To prepare drug molecules with specific structures, by virtue of the activity of halogen atoms, through nucleophilic substitution and other reactions, the required functional groups are introduced to build complex drug structures. For example, the synthesis of new drugs with antibacterial and antiviral effects, the unique structure of such compounds endows the drug with the specific binding ability to the target and enhances the efficacy.

In the field of materials science, it is also indispensable. Can participate in the creation of high-performance polymer materials. Because of its halogen atoms, it can improve the thermal stability, flame retardancy and other properties of materials. Such as the preparation of insulating materials used in electronic devices, after adding such compounds, the material's resistance to high temperature and flame is greatly increased, ensuring the safe operation of electronic equipment.

Furthermore, in the research and development of pesticides, 2-bromo-4-chloro-1-fluorobenzene can be used as a starting material to synthesize pesticides with high insecticidal and herbicidal properties. Through rational molecular design and the use of its halogen atom activity, pesticide molecules have high selectivity and toxic effect on specific pests or weeds, reduce the impact on the environment, and improve crop yield and quality. In conclusion, 2-bromo-4-chloro-1-fluorobenzene plays a key role in many important fields such as medicine, materials, and pesticides, promoting the development and progress of related industries.

What are 2-Bromo-4-chloro-1-fluorobenzene synthesis methods?

The synthesis method of 2-bromo-4-chloro-1-fluorobenzene is quite complicated and requires chemical principles and experimental skills. The common method is to use benzene as the starting material and undergo a halogenation reaction to introduce bromine, chlorine and fluorine atoms.

In the first step, benzene and bromine are brominated under the action of catalysts such as iron filings or iron tribromide to form bromobenzene. In this reaction, the bromine molecule is polarized by the catalyst and undergoes electrophilic substitution with the benzene ring, and the bromine atom replaces the hydrogen atom on the benzene ring. The chemical equation is:\ (C_ {6} H_ {6} + Br_ {2}\ xrightarrow [] {FeBr_ {3}} C_ {6} H_ {5} Br + HBr\).

In the second step, the obtained bromobenzene reacts with chlorine. In the presence of a suitable catalyst, such as iron trichloride, the chlorine atom replaces the hydrogen atom at a specific position on the bromobenzene ring to generate 4-chloro-2-bromobenzene. This is because the bromine atom is an ortho-para-locator, so that the chlorine atom mainly enters its ortho-para-position. The reaction formula is:\ (C_ {6} H_ {5} Br + Cl_ {2}\ xrightarrow [] {FeCl_ {3}} C_ {6} H_ {4} BrCl + HCl\).

In the last step, 4-chloro-2-bromobenzene reacts with fluorinated reagents, such as potassium fluoride, under specific solvents and conditions, and fluorine atoms replace specific hydrogen atoms on the benzene ring to obtain 2-bromo-4-chloro-1-fluorobenzene. This process requires attention to the control of reaction conditions, such as temperature, pressure, reaction time, etc., to ensure that the reaction proceeds in the direction of generating the target product. The reaction may be expressed as:\ (C_ {6} H_ {4} BrCl + KF\ xrightarrow [] {specific conditions} C_ {6} H_ {3} BrClF + KCl\).

There are also other synthesis paths, or fluorine atoms are introduced first, and then bromine and chlorine atoms are introduced in turn. However, each method needs to fine-tune the reaction conditions and consider the selectivity, yield and side reactions of each step in order to achieve the purpose of efficient synthesis of 2-bromo-4-chloro-1-fluorobenzene.

2-Bromo-4-chloro-1-fluorobenzene what are the precautions during storage and transportation?

2-Bromo-4-chloro-1-fluorobenzene is an organic compound. During storage and transportation, the following matters must be paid attention to:
- ** Storage **:
- ** Environment selection **: It should be placed in a cool and well-ventilated place. Because the compound is prone to chemical reactions or even decomposition when heated, a cool environment can effectively reduce such risks. Well-ventilated can avoid safety hazards caused by gas accumulation.
- ** Container selection **: Containers with excellent sealing performance should be used. 2-Bromo-4-chloro-1-fluorobenzene has certain volatility and chemical activity. A sealed container can prevent its volatilization and escape, and can also avoid reaction with external substances. And the container material should not chemically react with the compound. Glass containers are usually a good choice, but it is necessary to pay attention to their compatibility with certain chemicals under specific conditions.
- ** Keep away from contraindications **: Do not co-store with oxidizing agents, strong bases, etc. 2-Bromo-4-chloro-1-fluorobenzene is prone to violent oxidation reactions when it encounters oxidants, and may cause chemical reactions such as hydrolysis when it encounters strong bases, which may cause material deterioration and even lead to safety accidents.
- ** Transportation **:
- ** Packaging Stable **: Transportation packaging must be firm and reliable. Ensure that even in the event of bumps or collisions during transportation, the packaging will not be damaged, so as to avoid leakage of 2-bromo-4-chloro-1-fluorobenzene. Appropriate cushioning materials can be used to reinforce and protect the packaging. < Br > - ** Clear marking **: The name of the substance, hazardous characteristics and other information should be clearly marked on the outside of the package. In this way, transportation personnel and supervisors can quickly know its nature, and in the event of an accident, they can take appropriate measures in a timely manner.
- ** Compliance with regulations **: The transportation process must strictly follow relevant laws and regulations. Such as specific routes and time regulations for the transportation of hazardous chemicals must be strictly followed to ensure the safety of the transportation process and prevent harm to the environment and the public.
- ** Professional personnel **: The person responsible for transportation should have professional knowledge and be familiar with the dangerous characteristics of 2-bromo-4-chloro-1-fluorobenzene and emergency treatment methods. In the event of an emergency such as a leak during transportation, it can be dealt with quickly and correctly to minimize losses and hazards.

What are the effects of 2-Bromo-4-chloro-1-fluorobenzene on the environment and human health?

2-Bromo-4-chloro-1-fluorobenzene is an organohalogenated aromatic compound. The impact of these compounds on the environment and human health has long attracted the attention of the world.

At the environmental level, 2-bromo-4-chloro-1-fluorobenzene has certain stability and is difficult to be rapidly degraded by the natural environment. It can enter the natural environment through industrial emissions, waste disposal, etc., and remain in soil, water and atmosphere. In soil, it may interfere with the normal function of soil microbial communities, hinder the material cycle and energy conversion of soil ecosystems, and then affect plant growth and development. In water, due to its hydrophobicity, or adsorption to suspended particles, it settles to the sediment at the bottom of the water, posing a long-term threat to aquatic organisms. If aquatic organisms are exposed to this compound for a long time, it may cause physiological disorders, such as affecting the respiratory system and nervous system of fish, hindering their normal growth and reproduction, and even causing population reduction.

As for human health, 2-bromo-4-chloro-1-fluorobenzene can enter the human body through the respiratory tract, skin contact and food chain intake. Inhalation through the respiratory tract can directly affect the respiratory system, causing symptoms such as cough, asthma, breathing difficulties, etc. Skin contact or cause skin allergies, inflammation, erythema, itching, blisters, etc. In particular, this compound may have potential toxicity and carcinogenicity. After entering the human body, it may interfere with the human endocrine system, affect the normal secretion and regulation of hormones, and have adverse effects on the reproductive system and immune system. Long-term low-dose exposure may increase the risk of cancer, threatening human life and health.

Therefore, for 2-bromo-4-chloro-1-fluorobenzene compounds, we should treat them with caution and strengthen monitoring and control to protect the environment and human health.