2 Chloro 3 Nitrobenzotrifluoride
Fluoride
2-Chloro-3-nitrobenzotrifluoride
Chemical Formula C7H3ClF3NO2
Molecular Weight 225.55
Appearance Liquid (usually)
Color Colorless to pale yellow
Odor Characteristic odor
Boiling Point Around 225 - 227 °C
Solubility In Water Low solubility in water
Solubility In Organic Solvents Soluble in many organic solvents
Vapor Pressure Low vapor pressure at room temperature
Stability Stable under normal conditions
Hazard Class May be a hazardous chemical
FAQ

What are the main uses of 2-Chloro-3-nitrobenzotrifluoride?

2-Chloro-3-nitrotrifluorotoluene, which has a wide range of uses and is a key raw material in the field of organic synthesis.

First, in the creation of medicine, it is often used as a starting material for the synthesis of drug molecules with special structures. Due to its unique functional groups, it can construct structural fragments with specific physiological activities through various chemical reactions. For example, through a series of delicate operations such as halogenation reaction, nitro reduction reaction, and nucleophilic substitution reaction, novel compounds with antibacterial, anti-inflammatory or anti-tumor activities can be derived, opening up new paths for pharmaceutical research and development.

Second, in the field of pesticides, it is also of important value. With its chemical properties, efficient and low-toxic pesticide varieties can be designed and synthesized. For example, through reasonable molecular modification, it exhibits excellent biological activity against specific pests or weeds, and has little impact on the environment, which is in line with the current needs of green agriculture development.

Furthermore, in the field of materials science, 2-chloro-3-nitrotrifluorotoluene is also possible. The polymer materials involved in the synthesis may have special physical and chemical properties, such as excellent heat resistance and chemical stability. These materials can be used in high-end fields such as aerospace and electronics to meet the strict requirements of material properties in specific environments.

In conclusion, 2-chloro-3-nitrotrifluorotoluene plays an indispensable role in many fields such as organic synthesis, medicine, pesticides, and materials science, promoting technological innovation and development in various fields.

What are the physical properties of 2-Chloro-3-nitrobenzotrifluoride?

2-Chloro-3-nitrotrifluorotoluene is one of the organic compounds. It has unique physical properties, let me tell you in detail.

Looking at its appearance, it is often colorless to light yellow liquid. Under the sun, it has a faint luster and flows, just like a sparkling lake. Its smell is quite special, and ordinary people smell it, or feel pungent and irritating. However, for Fangjia who is good at chemistry, this is also one of the characteristics to distinguish its properties. < Br >
When it comes to the boiling point, it is about a certain numerical range. At this temperature, the substance converts from liquid to gaseous state, just like ice melts into water, and water reconverts into water vapor. This is the beauty of the transformation of the state of matter. And its melting point makes the substance solidify from liquid to solid state in a specific low temperature environment, just like water turns into ice when it is cold, and the physical properties are fully apparent between the morphological changes.

Compared with water, its density has its own unique value. In many chemical reactions and practical applications, this density characteristic is related to the mixing and stratification of substances, which is extremely critical. In terms of solubility, 2-chloro-3-nitrotrifluorotoluene is soluble in certain organic solvents, such as some alcohols and ether solvents, just like salts are integrated into water and dispersed uniformly, while in water it has poor solubility. This property also affects its behavior in different systems.

In addition, the vapor pressure of the substance is also one of its important physical properties. The vapor pressure reflects its tendency to evaporate into a gaseous state at a certain temperature. The higher the vapor pressure, the more volatile it is under the same conditions, just like a fragrant wine. The aroma molecules are easy to evaporate and disperse. The same is true for the steam of 2-chloro-3-nitrotrifluorotoluene, which gradually diffuses in the air. The characteristics of its vapor pressure have an impact on its storage and use environment.

What is the chemistry of 2-Chloro-3-nitrobenzotrifluoride?

2-Chloro-3-nitrotoluene is an important compound in the field of organic synthesis. Its chemical properties are unique and have a variety of remarkable characteristics.

First of all, the reactivity of halogen atoms is discussed. This compound contains chlorine atoms. In halogenated aromatics, chlorine atoms can participate in many nucleophilic substitution reactions. Due to the influence of aromatic ring electron clouds, the activity of chlorine atoms is slightly lower than that of halogen atoms in aliphatic halogenated hydrocarbons. However, under suitable conditions, such as high temperature, strong bases or the presence of specific catalysts, chlorine atoms can be replaced by nucleophilic reagents. For example, when reacting with sodium alcohol, chlorine atoms can be replaced by alkoxy groups to form corresponding ether compounds; when reacting with ammonia or amines, nitrogen-containing derivatives can be obtained.

Re-examining the properties of nitro groups. Nitro is a strong electron-absorbing group, and its existence greatly reduces the electron cloud density of aromatic rings, and the electrophilic substitution activity of aromatic rings is significantly reduced. At the same time, nitro groups can undergo reduction reactions. Under the action of suitable reducing agents such as iron filings and hydrochloric acid, hydrogen and catalysts, nitro groups can be gradually reduced to amino groups, which is an important way to prepare amino-containing aromatic compounds. And due to the strong electron-absorbing effect of nitro groups, the electron cloud density of ortho and para-carbon atoms is lower, which affects the activity of chlorine atoms and makes nucleophilic substitution reactions more likely to occur at chlorine atoms.

As for trifluoromethyl groups, they are strong electron-absorbing groups and have far-reaching effects on the physical and chemical properties of compounds. It can enhance the lipid solubility of molecules and affect the polarity of compounds. In chemical reactions, trifluoromethyl can reduce the electron cloud density of aromatic rings, further affecting the reactivity of aromatic rings. In addition, the presence of trifluoromethyl can improve the stability of compounds. Under certain reaction conditions, the entire molecular structure can be more stable, and it is not easy to decompose or rearrange.

In short, the chemical properties of 2-chloro-3-nitrotrifluorotoluene are determined by the interaction of chlorine atoms, nitro groups and trifluoromethyl groups, which make it important in the fields of organic synthesis, pharmaceutical chemistry and materials science.

What are the preparation methods of 2-Chloro-3-nitrobenzotrifluoride?

There are many different methods for preparing 2-chloro-3-nitrotrifluorotoluene. One method can be obtained from 2-chloro-3-aminotrifluorotoluene by diazotization and nitrification. First, 2-chloro-3-aminotrifluorotoluene reacts with sodium nitrite and acid to form diazonium salts. This process requires temperature control, so that the temperature is not too high to cause the decomposition of diazonium salts. After that, the diazonium salt and the nitrifying reagent, such as the mixed acid of nitric acid and sulfuric acid, are slowly mixed and nitrified, resulting in 2-chloro-3-nitrotrifluorotoluene.

Another method is to use 2-chlorotrifluorotoluene as the starting material. First, it is nitrified with a mixed acid, and a nitro group is introduced to obtain a mixture of 2-chloro-3-nitrotrifluorotoluene and other nitroisomers. After separation, such as column chromatography or distillation, the target product 2-chloro-3-nitrotrifluorotoluene is separated from the mixture.

Or starting from trifluorotoluene, chlorinated first to obtain a chlorine-containing trifluorotoluene derivative, and then nitrified, 2-chloro-3-nitrotrifluorotoluene can also be obtained. When chlorinating, chlorine and a suitable catalyst can be selected to determine the chlorination position. In the nitrification step, the reaction conditions are finely adjusted according to the conventional method of mixed acid nitrification, so that the nitro group is exactly at the desired position.

The preparation process requires careful treatment of all conditions. The proportion of reactants, reaction temperature, and reaction time are all related to the yield and purity of the product. And the operation of each step must also follow the specifications to ensure the safety and success of the experiment.

What 2-Chloro-3-nitrobenzotrifluoride need to pay attention to when storing and transporting

2-Chloro-3-nitrotrifluorotoluene is an organic compound. When storing and transporting, many key matters need to be paid attention to to to ensure safety and avoid accidents.

Bear the brunt. When storing, be sure to choose a cool, dry and well-ventilated place. This compound is more sensitive to heat, and high temperature environments can easily cause it to decompose, which can cause danger. If placed in a humid place, moisture may react with the compound chemically, resulting in deterioration of quality or even the formation of dangerous products.

Furthermore, this compound is toxic and irritating, and it needs to be strictly sealed when stored to prevent leakage, thereby avoiding harm to the surrounding environment and personnel. At the same time, warning signs should be prominently posted in the storage area to make everyone aware of its potential danger.

During transportation, the same should not be taken lightly. It needs to be properly fixed to prevent packaging damage due to bumps and collisions, resulting in compound leakage. And the means of transportation should also be dry, ventilated, and away from fire and heat sources.

In addition, whether it is storage or transportation, relevant regulations and standards must be strictly followed. Operators need to be professionally trained and familiar with the characteristics of the compound and emergency treatment methods. In the event of an unexpected situation such as a leak, they can take prompt and correct response measures, such as evacuating personnel, sealing off the scene, and handling leaks, to minimize harm.

Only by paying careful attention to the above matters during the storage and transportation of 2-chloro-3-nitrotrifluorotoluene can the safety of personnel and the environment be guaranteed.