2 Chloro 4 Fluorobenzene 1 Carbonyl Chloride
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Chloro-4-fluorobenzene-1-carbonyl chloride
Chemical Formula C7H3Cl2FO
Molecular Weight 193.00
Appearance Typically a colorless to light - yellow liquid
Boiling Point Around 200 - 210 °C (estimated, may vary with conditions)
Density Approximately 1.4 - 1.5 g/cm³ (estimated)
Solubility Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Low vapor pressure at room temperature
Flash Point Relatively high flash point, indicating low flammability risk
Reactivity Highly reactive, especially towards nucleophiles due to the presence of carbonyl chloride group
Chemical Formula C7H3Cl2FO
Molar Mass 193.002 g/mol
Appearance Typically a colorless to light - colored liquid
Boiling Point Around 220 - 230 °C (approximate, may vary with pressure)
Solubility Soluble in common organic solvents like dichloromethane, chloroform, etc., insoluble in water
Vapor Pressure Low at room temperature due to its relatively high boiling point
Reactivity Highly reactive, especially towards nucleophiles due to the presence of carbonyl chloride group
Name 2-Chloro-4-fluorobenzene-1-carbonyl chloride
Chemical Formula C7H3Cl2FO
Molar Mass 193.00 g/mol
Appearance Colorless to light yellow liquid
Density Data needed
Boiling Point Data needed
Melting Point Data needed
Solubility Soluble in common organic solvents
Flash Point Data needed
Purity Typically high - purity grades available, e.g., 95%+
Hazard Class Corrosive, harmful if swallowed, inhaled or in contact with skin
FAQ

What are the main uses of 2-Chloro-4-fluorobenzene-1-carbonyl chloride?

2-Chloro-4-fluorobenzoyl chloride is an extremely important chemical raw material in organic synthesis. It has a wide range of uses and plays a key role in many fields.

First, in the field of pharmaceutical synthesis, this compound is often used as a key intermediate. With its unique chemical structure, it can participate in a series of chemical reactions to help build complex drug molecular structures. For example, in the process of developing specific antibacterial drugs, 2-chloro-4-fluorobenzoyl chloride can react with other compounds containing functional groups such as nitrogen and oxygen, thus building a core skeleton with antibacterial activity. After a series of modifications and optimizations, highly effective antibacterial drugs can finally be prepared.

Second, in the field of pesticides, it also occupies an important position. It can be used to synthesize various types of pesticides, such as insecticides, herbicides, etc. By combining with different active groups, pesticide products with specific mechanisms of action and biological activities can be created. Taking the synthesis of new insecticides as an example, 2-chloro-4-fluorobenzoyl chloride reacts with specific amine compounds, and the resulting products may have unique neurotoxicity to some pests, thus effectively killing pests and ensuring the growth of crops.

Third, in the field of materials science, 2-chloro-4-fluorobenzoyl chloride also shows certain application potential. When preparing high-performance polymer materials, it can be introduced into the polymer chain as a functional monomer to endow the material with special properties, such as improving the heat resistance and chemical stability of the material. For example, when synthesizing special engineering plastics, adding an appropriate amount of 2-chloro-4-fluorobenzoyl chloride-derived monomer can improve the corrosion resistance and mechanical strength of the plastic, enabling it to be applied to harsher environments.

Fourth, in the synthesis of dyes, this compound can be used as an important starting material. Through a series of diazotization, coupling and other reactions, combined with different aromatic amines or phenolic compounds, dye products with bright colors and excellent fastness can be prepared, which are widely used in textile, printing and dyeing industries, giving fabrics a colorful color.

In summary, 2-chloro-4-fluorobenzoyl chloride is widely used in the fields of medicine, pesticides, materials science, dye synthesis, etc., and has an indispensable and important position in the field of organic synthetic chemistry.

What are the physical properties of 2-Chloro-4-fluorobenzene-1-carbonyl chloride?

2-Chloro-4-fluorobenzoyl chloride, this is an important compound in organic chemistry. Its physical properties are crucial and involve many chemical processes and studies.

Looking at its properties, it usually shows a colorless to pale yellow liquid state, with a uniform texture and no obvious impurities visible. Its odor is unique and irritating. It can feel a pungent smell when smelled. This pungent smell is due to the presence of chlorine and fluorine atoms in its chemical structure.

When it comes to boiling point, it is about a specific temperature range. Due to intermolecular forces, including van der Waals force and dipole-dipole interaction, it can change from liquid to gas at a certain temperature. This boiling point is crucial for the separation and purification of the compound. In distillation and other operations, precise control of the temperature to near the boiling point can achieve phase separation from other substances with different boiling points.

Melting point is also a key physical property. When the temperature drops to a certain extent, 2-chloro-4-fluorobenzoyl chloride will solidify from a liquid state to a solid state. The value of the melting point is the identification of its physical properties. For compounds of different purity, the melting point may be slightly different, so its purity can be judged.

In terms of solubility, 2-chloro-4-fluorobenzoyl chloride has good solubility in organic solvents such as dichloromethane and chloroform. This is due to the principle of "similar miscibility". The molecular structure of the compound has a certain similarity with organic solvents, and it can interact with organic solvent molecules and disperse them uniformly. However, its solubility in water is very poor. Due to the large difference between molecular polarity and water molecule polarity, it is difficult to form an effective interaction, so it is easy to stratify in an aqueous system.

Density is also a consideration. Its density is different from that of water. By measuring the density, it can also provide a reference for the identification of the compound and related chemical operations. In a mixed system, according to the density difference between it and other substances, suitable methods can be used for separation.

2-Chloro-4-fluorobenzene-1-carbonyl the chemical properties of chloride

2-Chloro-4-fluorobenzoyl chloride, this is an organic compound. Its chemical properties are unique and very active.

Looking at its structure, the chlorine atom and the fluorine atom are connected to the benzene ring, and the benzene ring is connected to the formyl chloride group. This structure gives it special reactivity.

Let's talk about its hydrolysis reaction first. When exposed to water, the formyl chloride group is easy to hydrolyze, resulting in corresponding carboxylic acids and hydrogen chloride. This reaction is violent. If you put it into water, it is like a dragon entering the water, and the waves rise. In an instant, the hydrogen chloride escapes, forming a white mist in the air, just like the morning fog in the mountains. This is because hydrogen chloride is very soluble in water and combines with water vapor in the air. < Br >
Let's talk about the reaction with alcohols. When it meets with alcohols, it is like a bosom friend meeting, and it reacts quickly to form esters and hydrogen chloride. This reaction is very important in organic synthesis and can be used to prepare various esters containing chlorine and fluorine. For example, in the field of fragrance and drug synthesis, it often plays a key role.

And the reaction with amines. When contacted with amines, the two react quickly like magnets, forming amides and hydrogen chloride. Amide compounds are widely used in many fields, and this reaction provides an effective way to prepare amides containing specific substituents. < Br >
Due to its active chemical properties, it plays a significant role in organic synthesis and can act as a key intermediate to help build many complex organic molecular structures. However, due to its intense reaction, extreme care must be taken during operation and strict procedures must be followed to prevent accidents.

What are the preparation methods of 2-Chloro-4-fluorobenzene-1-carbonyl chloride?

2-Chloro-4-fluorobenzoyl chloride is a commonly used reagent in organic synthesis. There are many preparation methods, and the following are common methods.

First, 2-chloro-4-fluorobenzoic acid is used as the starting material. First, 2-chloro-4-fluorobenzoic acid is placed in a reactor, and an appropriate amount of chlorination reagent is added, such as thionyl chloride ($SOCl_2 $). The two can react at an appropriate temperature, usually under the condition of heating and reflux. The function of thionyl chloride is to convert the carboxyl group ($-COOH $) into the acyl chloride group ($-COCl $). The reaction equation is as follows: $R - COOH + SOCl_2\ longrightarrow R - COCl + SO_2\ uparrow + HCl\ uparrow $, where $R $represents 2-chloro-4-fluorophenyl. After the reaction, the pure 2-chloro-4-fluorobenzoyl chloride can be separated by distillation and other operations.

Second, starting from 2-chloro-4-fluorotoluene. First, 2-chloro-4-fluorotoluene is oxidized to 2-chloro-4-fluorobenzoic acid in a suitable reaction environment, such as alkaline solution, with a suitable oxidant, such as potassium permanganate ($KMnO_4 $). Then, as the first method mentioned above, it is treated with thionyl chloride and converted into 2-chloro-4-fluorobenzoyl chloride. Although this approach is a little complicated, the raw material 2-chloro-4-fluorotoluene is relatively easy to obtain and is also one of the common preparation methods.

Third, 2-chloro-4-fluorobenzaldehyde is used as the raw material. First, a specific oxidation reaction is used to oxidize the aldehyde group ($-CHO $) to a carboxyl group to obtain 2-chloro-4-fluorobenzoic acid. Subsequent treatment with chlorination reagents can obtain the target product 2-chloro-4-fluorobenzoyl chloride. Optional oxidants include Jones reagent ($CrO_3 - H_2SO_4 $), etc., but attention should be paid to the control of reaction conditions to prevent side reactions such as excessive oxidation. < Br >
When preparing 2-chloro-4-fluorobenzoyl chloride, it is necessary to carefully select the appropriate preparation method according to many factors such as the availability of raw materials, cost, and difficulty in controlling reaction conditions, so as to achieve the purpose of efficient, economical and environmentally friendly preparation.

What are the precautions for 2-Chloro-4-fluorobenzene-1-carbonyl chloride in storage and transportation?

2-Chloro-4-fluorobenzoyl chloride is a chemical substance, and there are many things to pay attention to during storage and transportation.

This substance is highly corrosive and can cause serious damage to the human body and the environment. When storing, keep it in a cool, dry and well-ventilated place, keep it away from fire, heat sources, and direct sunlight. Because of its active chemical properties, it is easy to react with water, alcohol, and many other substances, so storage containers must be tightly sealed to avoid contact with moisture and other incompatible substances. It is advisable to store in containers made of corrosion-resistant materials such as glass, certain plastics, or metals (specially treated) to prevent leakage due to corrosion.

During transportation, relevant regulations and standards must also be strictly followed. It should be ensured that the packaging is firm and suitable packaging materials are used to resist vibration, collision and friction. Transportation vehicles should be equipped with corresponding emergency treatment equipment and protective equipment to prepare for leaks and other emergencies. Transportation personnel also need to be professionally trained to be familiar with the characteristics of the substance and emergency treatment methods. During transportation, it must not be mixed with food, medicine and other items to prevent contamination.

In the event of a leak, surrounding personnel should be evacuated immediately, and unrelated personnel should be strictly prohibited from approaching. Emergency personnel must wear professional protective equipment, such as protective clothing, gas masks, etc., to avoid direct contact with leaks. In the event of a small amount of leakage, it can be absorbed by inert materials such as sand, dry lime or soda ash and collected in a closed container. In the event of a large amount of leakage, a dike or pit should be built for containment, and a pump should be transferred to a tanker or a special collector for recycling or transportation to a waste treatment site for disposal.

In short, 2-chloro-4-fluorobenzoyl chloride must be stored and transported with high attention to safety and operated in strict accordance with regulations in order to effectively prevent accidents and ensure the safety of personnel and the environment.