1 Nitro 2 4 5 Trifluorobenzene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
1-Nitro-2,4,5-trifluorobenzene
Chemical Formula C6H2F3NO2
Appearance Colorless to light yellow liquid
Boiling Point Around 175 - 177 °C
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
Vapor Pressure Low vapor pressure at room temperature
Chemical Formula C6H2F3NO2
Molar Mass 181.08 g/mol
Appearance Colorless to light yellow liquid
Boiling Point 175 - 177 °C
Melting Point N/A
Density 1.52 g/cm³
Solubility In Water Insoluble
Vapor Pressure N/A
Flash Point 72 °C
Refractive Index 1.463 (20 °C)
Chemical Formula C6H2F3NO2
Molar Mass 179.08 g/mol
Appearance Colorless to light yellow liquid
Boiling Point 175 - 177 °C
Melting Point N/A
Density 1.529 g/cm³
Solubility In Water Insoluble
Solubility In Organic Solvents Soluble in common organic solvents like ethanol, ether
Flash Point 70 °C
Vapor Pressure N/A
Refractive Index 1.465
FAQ

What are the main uses of 1-Nitro-2,4,5-trifluorobenzene?

1-Nitro-2,4,5-trifluorobenzene, Chinese name 1-nitro-2,4,5-trifluorobenzene, is a crucial raw material in the field of organic synthesis and is widely used in medicine, pesticides, materials and other industries.

In the field of medicine, this compound is mainly used to prepare various specific drugs. Due to its unique chemical structure, it can interact with specific targets in organisms and exhibit excellent pharmacological activity. For example, it can be used as a key intermediate to participate in the synthesis of drugs with antibacterial and antiviral effects. In the development of new antimicrobial drugs, 1-nitro-2,4,5-trifluorobenzene can construct molecular structures that are highly compatible with bacterial cell walls or protein synthesis-related targets through a series of chemical reactions, thereby effectively inhibiting bacterial growth and reproduction, providing a powerful weapon for the clinical treatment of bacterial infectious diseases.

In the pesticide industry, 1-nitro-2,4,5-trifluorobenzene also plays a pivotal role. With the help of its synthetic pesticides, it has many advantages such as high efficiency, low toxicity and environmental friendliness. For example, pesticides that can be synthesized for specific pests can precisely act on the nervous system or physiological metabolic processes of pests by virtue of their special chemical properties, causing paralysis and death of pests, while having little impact on the environment and non-target organisms, which effectively guarantees the safety of agricultural production and the stability of the ecological environment.

In the field of materials science, 1-nitro-2,4,5-trifluorobenzene can be used to prepare high-performance functional materials. For example, by polymerizing with other monomers, it can endow materials with special properties such as excellent heat resistance and chemical stability. Applied to the aerospace field, the prepared materials can meet the strict requirements of material properties in extreme environments of aircraft, ensuring the safe and reliable operation of aircraft.

In summary, 1-nitro-2,4,5-trifluorobenzene plays an indispensable role in many important industries due to its unique chemical structure and reactivity, and is of great significance for promoting technological progress and innovation in various industries.

What are the physical properties of 1-Nitro-2,4,5-trifluorobenzene?

1-Nitro-2,4,5-trifluorobenzene is a kind of organic compound. Its physical properties are quite important and meaningful in many fields such as chemical industry.

First of all, its appearance, at room temperature, is often colorless to light yellow liquid, clear and has a special smell. This smell is unique, but also pungent, and the smell is alarming.

When it comes to the melting point, it is about -20 ° C, depending on the measurement environment or slightly variable. The melting point is low, so it is liquid at room temperature. The boiling point is between 180-190 ° C. When the temperature reaches this range, the substance changes from liquid to gaseous state.

In terms of density, it is about 1.6 g/cm ³, which is heavier than water. If mixed with water, it will sink to the bottom of the water.

In terms of solubility, it can be well dissolved in organic solvents such as ethanol and ether. However, in water, the solubility is extremely low. Due to the characteristics of molecular structure, the interaction with water is weak.

Furthermore, 1-nitro-2,4,5-trifluorobenzene has low volatility and is not easy to evaporate quickly into the air at room temperature and pressure. However, although the volatility is low, it still has a certain vapor pressure. In confined spaces or high temperature environments, it is necessary to pay attention to the risk of vapor accumulation.

In addition, the substance is sensitive to light and heat. Excessive exposure to light or heat may cause changes in its chemical structure and cause reactions such as decomposition. Therefore, when storing, it should be placed in a cool, dark place and away from heat sources.

What are the chemical properties of 1-Nitro-2,4,5-trifluorobenzene?

1 - Nitro - 2,4,5 - trifluorobenzene is an organic compound with interesting chemical properties, which are described in detail today.

This compound contains nitro and fluorine atoms, and its structure is unique, which makes it have special chemical activity. Nitro is a strong electron-absorbing group, which can reduce the electron cloud density of the benzene ring, making the benzene ring more prone to nucleophilic substitution reactions. For example, nucleophilic reagents such as alkoxides and amines can be substituted with fluorine atoms on the benzene ring.

Fluorine atoms also have a profound impact on their chemical properties. Fluorine atoms are extremely electronegative and are connected to the benzene ring, which makes the C-F bond energy greater and has good stability. However, due to its strong electron-absorbing effect, it can activate the adjacent and para-sites on the benzene ring. Although the overall electron cloud density decreases, it makes the specific location more vulnerable to nucleophilic reagents.

1 - Nitro - 2,4,5 - trifluorobenzene can undergo reduction reaction under appropriate conditions. Nitro can be reduced to amino groups to form amino-containing fluoroaromatic hydrocarbons. The product is widely used in the field of medicine and pesticide synthesis, and can be used as a key intermediate to construct complex molecular structures.

Its reaction with metal-organic reagents can realize arylation, expand the molecular skeleton, and provide an effective way to construct new carbon-carbon bonds in organic synthesis. Synthesize organic materials with specific functions.

In addition, under alkaline conditions, 1-Nitro-2,4,5-trifluorobenzene can undergo hydrolysis, in which fluorine atoms may be replaced by hydroxyl groups to form compounds containing nitro and hydroxyl groups. Such compounds are of great value in drug development and fine chemical synthesis.

1-Nitro-2,4,5-trifluorobenzene has active chemical properties and has important application potential in organic synthesis, pharmaceutical chemistry, materials science and other fields. Studying its reaction properties is of great significance for the development of new synthesis methods and functional materials.

What is the preparation method of 1-Nitro-2,4,5-trifluorobenzene?

The preparation method of 1-nitro-2,4,5-trifluorobenzene has been known for a long time, and is described in detail as follows.

First, 2,4,5-trifluorobenzene is used as the starting material. Dissolve 2,4,5-trifluorobenzene in an appropriate amount of sulfuric acid and slowly add sodium nitrite solution at low temperature. This process requires strict temperature control to ensure that the reaction proceeds smoothly. This is a diazotization reaction. When the diazotization reaction is complete, add an appropriate amount of sodium fluoroborate solution to generate 2,4,5-trifluorobenzene diazo fluoroborate precipitation. Filter and collect the precipitation, wash it thoroughly, and dry it. Heat and decompose the dried 2,4,5-trifluorobenzene diazo fluoroborate to obtain 1-nitro-2,4,5-trifluorobenzene. Although this method is complicated, it can be obtained by proper operation.

Second, 2,4,5-trifluorotoluene is used as raw material. First, 2,4,5-trifluorotoluene is heated with a mixed acid system composed of concentrated nitric acid and concentrated sulfuric acid. The ratio of mixed acid, reaction temperature and time are all key factors. Nitric acid is used as a nitrifying reagent here, while sulfuric acid plays a catalytic and dehydrating role. During the reaction process, close attention should be paid to the reaction process, and monitoring means should be used to ensure the appropriate reaction. After the reaction is completed, 1-nitro-2,4,5-trifluorobenzene can be obtained through a series of post-treatment processes such as cooling, liquid separation, washing and drying. This path is relatively direct, so the mixed acid needs to be handled carefully to ensure safety.

Third, use 1,2,4-trifluorobenzene as the starting material. First, 1,2,4-trifluorobenzene and acetylation reagents (such as acetic anhydride) are acylated by Fu-gram under the catalysis of Lewis acid (such as aluminum trichloride) to generate 2,4,5-trifluoroacetophenone. Then, 2,4,5-trifluoroacetophenone is nitrified by nitrifying reagents (such as a mixture of nitric acid and acetic anhydride) to introduce nitro groups. Finally, the acetyl group is removed by suitable methods (such as hydrolysis under basic conditions, oxidation, etc.) to obtain 1-nitro-2,4,5-trifluorobenzene. This method has many steps, but the reaction conditions in each step are relatively mild and can be completed using common reagents.

What are the precautions for storing and transporting 1-Nitro-2,4,5-trifluorobenzene?

1-Nitro-2,4,5-trifluorobenzene is a chemical substance. During storage and transportation, many matters must be paid attention to.

Its properties are dangerous, and when storing, the first environment. When placed in a cool and ventilated warehouse, away from fire and heat sources, this is to avoid risks caused by heat. The temperature of the warehouse should be controlled, not too high, to prevent changes in its chemical properties.

Furthermore, it should be stored separately from oxidizing agents, reducing agents, alkalis, etc., and must not be mixed. It may react violently with such substances, causing explosions, fires and other disasters.

Packaging must also be rigorous. Ensure that the packaging is complete and there is no risk of damage and leakage. Packaging materials should be resistant to corrosion and have a certain strength to ensure stability during storage.

When transporting, there are also many precautions. Transportation vehicles should be equipped with corresponding varieties and quantities of fire equipment and leakage emergency treatment equipment. During driving, it is necessary to prevent exposure to the sun, rain and high temperature.

Drivers and escorts must be familiar with their nature and emergency disposal methods. During transportation, do not park at will, and avoid staying near densely populated areas and important facilities.

When loading and unloading, the operation should be light and light, and it is strictly forbidden to drop and heavy pressure to prevent package damage from causing it to leak.

All of these are important items to be paid attention to when storing and transporting 1-nitro-2,4,5-trifluorobenzene. If there is a slight fear, it will cause a disaster, and it should not be careless.