2 Chloro 4 Fluorobenzene 1 Sulfonyl Chloride
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
2-Chloro-4-fluorobenzene-1-sulfonyl chloride
Name 2-Chloro-4-fluorobenzene-1-sulfonyl chloride
Chemical Formula C6H3Cl2FO2S
Molar Mass 231.056 g/mol
Appearance A colorless to pale yellow liquid
Boiling Point Around 268 - 270 °C
Density Approx. 1.65 g/cm³
Solubility Reacts with water, soluble in some organic solvents like dichloromethane
Cas Number 2106-07-8
Purity Can be obtained in high purity for commercial use
Reactivity Reactive towards nucleophiles due to the presence of sulfonyl chloride group
Chemical Formula C6H3Cl2FO2S
Molecular Weight 231.055 g/mol
Appearance A colorless to light yellow liquid
Boiling Point Around 280 - 285 °C
Density Approx. 1.65 g/cm³
Solubility In Water Reacts with water
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, toluene
Pungency Highly pungent odor
Hazard Class Corrosive, toxic
Name 2-Chloro-4-fluorobenzene-1-sulfonyl chloride
Chemical Formula C6H3Cl2FO2S
Molar Mass 231.056 g/mol
Appearance A colorless to light yellow liquid
Boiling Point Around 260 - 265 °C
Solubility Soluble in common organic solvents like dichloromethane
Pungency Strong, irritating odor
Reactivity Reactive towards nucleophiles like amines and alcohols
FAQ

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

2-Chloro-4-fluorobenzene-1-sulfonyl chloride is a crucial chemical raw material in the field of organic synthesis. It has a wide range of uses and plays a key role in medicine, pesticides, materials science and many other aspects.

In the synthesis of medicine, this compound is often used as a key intermediate. Due to the unique activity of chlorine, fluorine and sulfonyl chloride groups in its structure, it can replace various compounds containing heteroatoms such as nitrogen, oxygen and sulfur, and then build a complex drug molecular skeleton. For example, sulfonamide derivatives can be formed by reacting with amine compounds. Many of these derivatives exhibit significant biological activities, such as antibacterial, anti-inflammatory, and anti-tumor effects, which are of great significance in the development of new drugs.

In the process of pesticide creation, 2-chloro-4-fluorobenzene-1-sulfonyl chloride also plays an indispensable role. By reacting with specific alcohols, phenols, or amines, pesticide varieties with high insecticidal, bactericidal, or herbicidal properties can be prepared. Due to the novel structure of the derived pesticides, they can target specific pests or weeds, and have relatively little impact on the environment, so they are very popular. < Br >
In the field of materials science, this compound can be used to prepare polymer materials with special properties. Its sulfonyl chloride group can cross-link with polymers containing hydroxyl groups and amino groups to improve the mechanical properties, thermal stability and chemical stability of the material. For example, when preparing high-performance engineering plastics, coatings or adhesives, adding an appropriate amount of 2-chloro-4-fluorobenzene-1-sulfonyl chloride derivatives can significantly improve the comprehensive properties of the material and expand its application field.

In summary, 2-chloro-4-fluorobenzene-1-sulfonyl chloride has shown great application prospects in many important fields due to its unique chemical structure and reactivity, and has made great contributions to the development of related industries.

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

2-Chloro-4-fluorobenzene-1-sulfonyl chloride is an important compound in organic chemistry. It has unique physical properties and is worth exploring.

First of all, its appearance, at room temperature, often appears colorless to slightly yellow liquid, which is clearly recognizable and observable. Its odor, with strong irritation and pungent smell, is one of its remarkable characteristics, which is difficult to ignore.

When it comes to boiling point, it is in a higher temperature range due to molecular structure and interaction force, but the exact value may vary depending on experimental conditions. This boiling point characteristic is extremely critical in the process of separation and purification, and is an important basis for chemical operation.

Its density is also an important physical property. The relative density is greater than that of water, which means that it will sink to the bottom in water. This property is of great significance when it comes to operations such as liquid-liquid separation.

In terms of solubility, 2-chloro-4-fluorobenzene-1-sulfonyl chloride is soluble in many organic solvents, such as common ether, dichloromethane, etc. This solubility gives it a wide range of applications in organic synthesis reactions. With the help of suitable solvents, it can fully participate in the reaction and improve the efficiency and effect of the reaction.

In addition, the compound is sensitive to air and humidity. In the air, or due to oxidation and other reactions and deterioration; in case of moisture, it is prone to hydrolysis reactions, resulting in changes in its own structure and properties. Therefore, when storing, it needs to be properly sealed and placed in a dry environment to prevent its properties from changing and ensure its chemical activity and purity.

In summary, the physical properties of 2-chloro-4-fluorobenzene-1-sulfonyl chloride, such as appearance, odor, boiling point, density, solubility, and sensitivity to air and humidity, have a crucial impact on its organic synthesis, storage, and application.

What are the chemical synthesis methods of 2-Chloro-4-fluorobenzene-1-sulfonyl chloride?

To prepare 2-chloro-4-fluorobenzene-1-sulfonyl chloride, there are two methods. First, start with 2-chloro-4-fluorobenzene, and first go through the sulfonation step. In an appropriate reactor, add 2-chloro-4-fluorobenzene, use fuming sulfuric acid as a sulfonating agent, and control the temperature in a specific range, usually about 60 to 80 degrees Celsius. At this time, the hydrogen atom on the benzene ring is replaced by a sulfonic acid group to obtain 2-chloro-4-fluorobenzene sulfonic acid. Thereafter, the sulfonic acid product is heated with phosphorus pentachloride or dichlorosulfoxide. If phosphorus pentachloride is used, the reaction is intense, and the temperature needs to be carefully controlled, about 80 to 100 degrees Celsius. The hydroxyl group of the sulfonic acid group is a chlorine atom, so 2-chloro-4-fluorobenzene-1-sulfonyl chloride is obtained.

Second, use 2-chloro-4-fluorobenzene as the starting material. First, it is co-reacted with sodium nitrite and hydrochloric acid, and at low temperature, generally 0 to 5 degrees Celsius, the diazotization reaction is carried out to obtain diazonium salt. The diazonium salt is co-heated with sodium sulfite and copper sulfate, and the sulfonic acid group is introduced through the Sandmeier reaction variant to obtain the intermediate of 2-chloro-4-fluoroben Subsequent reaction with phosphorus pentachloride or sulfoxide chloride, with the previous method, the sulfonic acid group is converted into sulfonyl chloride, and the final product is 2-chloro-4-fluorobenzene-1-sulfonyl chloride. Each method has its advantages and disadvantages, depending on the availability of raw materials, the difficulty of reaction conditions and other factors, choose the best one.

2-Chloro-4-fluorobenzene-1-sulfonyl chloride during storage and transportation

2-Chloro-4-fluorobenzene-1-sulfonyl chloride is a chemical substance, and caution must be taken when storing and transporting it.

It is active and easy to react violently in contact with water. Therefore, the storage place must be extremely dry, away from shady places, away from water sources, and the humidity of the warehouse should be controlled at a low degree, so as not to be disturbed by water vapor.

This substance is sensitive to heat, easily decomposed by heat, or dangerous. The storage temperature should be low, and it should not be exposed to sunlight, nor should it be near heat sources and fire sources, such as heaters and open flames.

2-Chloro-4-fluorobenzene-1-sulfonyl chloride is highly corrosive and can erode a variety of materials. The container used for storage must be corrosion-resistant, such as glass, specific plastic or metal materials, and the container must be well sealed to prevent leakage.

When transporting, it is also necessary to strictly abide by the specifications. The packaging must be solid and reliable, able to withstand vibration and collision, and avoid damage. The transportation vehicle needs to be equipped with emergency treatment equipment in case of leakage, which can be dealt with in time. The escort must be familiar with the characteristics of this substance and emergency measures, and often inspect the package on the way to see if there is any damage or leakage.

In short, the storage and transportation of 2-chloro-4-fluorobenzene-1-sulfonyl chloride should be carried out under dry, cool, heat-proof and sealed conditions, in accordance with professional laws, to ensure the safety of personnel and the environment.

What are the effects of 2-Chloro-4-fluorobenzene-1-sulfonyl chloride on the environment and human body?

2-Chloro-4-fluorobenzene-1-sulfonyl chloride is a commonly used reagent in organic synthesis. Its impact on the environment and human body is particularly important and needs to be reviewed in detail.

At the end of the environment, if released in nature, this compound can cause multiple hazards. Its chemical properties are active, or it reacts with surrounding substances to change the chemical balance. If it flows into water bodies, it will endanger aquatic organisms. Because of its toxicity, or cause damage to physiological functions such as fish and plankton, it affects the food chain and community structure of aquatic ecology. In soil, it may affect the activity and community composition of soil microorganisms, and hinder the normal ecological functions of soil, such as nutrient cycling and decomposition of organic matter. And because of its high stability, or long-term residual in the environment, it continues to produce negative effects.

As for the human body, exposure to this compound can cause a variety of adverse consequences. Through skin contact, it can cause irritation and allergic reactions, causing skin redness, swelling, itching and even burns. If inadvertently inhaled, it will irritate the respiratory tract, causing symptoms such as cough, asthma, breathing difficulties, and even damage lung tissue and affect respiratory function. If eaten by mistake, it can cause serious damage to the digestive system, corrode the oral, esophageal and gastric mucosa, causing severe pain, vomiting, diarrhea, etc. Long-term exposure or exposure is more likely to be potentially carcinogenic, harm the genetic material of human cells, and increase the risk of cancer.

In conclusion, 2-chloro-4-fluorobenzene-1-sulfonyl chloride poses significant potential hazards to the environment and human body. When using and disposing of it, strict safety procedures and environmental protection requirements must be followed to reduce its negative effects and protect the environment and human safety.