3 Amino Alpha Alpha Alpha Trifluorotoluene
Fluorine Difluoride Fluorobenzene Fluorobenzyl Trifluorotoluene
3-amino-alpha,alpha,alpha-trifluorotoluene
Molecular Formula C7H6F3N
Molecular Weight 161.12
Appearance Typically a colorless to light - yellow liquid
Boiling Point Around 170 - 175°C
Density Approximately 1.24 g/cm³
Vapor Pressure Low vapor pressure at room temperature
Solubility Slightly soluble in water, soluble in organic solvents like ethanol, ether
Flash Point Around 60°C
Refractive Index Typically around 1.45
FAQ

What is the main use of 3-amino-alpha, alpha, alpha-trifluorotoluene?

3-Amino -α,α,α - trifluorotoluene, or 3-amino-trifluorotoluene, is widely used.

In the field of pharmaceutical synthesis, it is often a key intermediate. Due to the unique characteristics of fluorinated organic compounds in pharmaceutical chemistry, the introduction of fluorine atoms can significantly change the physical, chemical and biological activities of compounds. Using this substance as a starting material, a series of chemical reactions can be used to prepare a variety of drugs with specific pharmacological activities. For example, in the synthesis of some antidepressants, 3-amino-trifluorotoluene is ingeniously chemically modified to introduce other specific functional groups, which can obtain drug molecules with unique neuroregulatory effects. By modulating the transmission of neurotransmitters, it can achieve the effect of treating depression symptoms.

In the field of pesticides, it also plays an important role. With the increasing demand for high-efficiency and low-toxicity pesticides in modern agriculture, fluorinated pesticides are favored because of their high activity and low residue. 3-amino-trifluorotoluene can be used as an important building block for the synthesis of such pesticides. Pesticide molecules based on it can exhibit highly selective inhibition or killing effects on specific pests or weeds. For example, for some stubborn weeds, the herbicide synthesized from this raw material can precisely act on the specific physiological process of weeds, such as interfering with their photosynthesis or cell division, so as to efficiently control the growth of weeds, and has little impact on the environment and non-target organisms.

In addition, in the field of materials science, 3-amino-trifluorotoluene is also used. It can be used to prepare polymer materials with special properties. Introducing it into the structure of a polymer, with the strong electronegativity of fluorine atoms and special electronic effects, can endow polymer materials with properties such as excellent chemical resistance and low surface energy. Such materials can be used in coatings, plastics, and other fields, such as the preparation of corrosion-resistant high-performance coatings, which are used for equipment protection in harsh environments to extend the service life of equipment; or the preparation of plastics with low friction coefficients, which are used to manufacture specific mechanical components, reduce friction losses, and improve mechanical operation efficiency.

What are the physical properties of 3-amino-alpha, alpha, alpha-trifluorotoluene

3 - amino -α,α,α - trifluorotoluene, is a kind of organic compound. Its physical properties are very descriptive.

Under normal temperature and pressure, it is often colorless to light yellow liquid, with a clear appearance and a certain fluidity. The smell of this substance often has a special aroma, although it is not pungent, it is also recognizable.

As for the boiling point, it is within a certain temperature range. Due to the characteristics of intermolecular forces and structures, the boiling point has a specific value, which is crucial for its phase transition under different conditions. During the heating process, when the temperature rises to the boiling point, it will change from liquid to gaseous state. The melting point of

is also an important physical property. The specific melting point makes the compound tend to exist in the solid state when it is lower than this temperature. The melting point is determined by factors such as intermolecular interactions and crystal structure.

Solubility cannot be ignored. In organic solvents, such as common ethanol, ether, etc., it exhibits good solubility. This is based on the principle of similar compatibility. Due to the characteristics of molecular structure, it can form suitable interactions with organic solvent molecules. However, the solubility in water is relatively limited, due to the difference between the polarity of water and the molecular polarity of the compound, and the interaction is weak.

In addition, its density is also a key physical property. Compared with water, it has a specific density value, which affects its distribution and behavior in liquid mixtures. The density is related to the mass of molecules and the degree of close arrangement between molecules.

Furthermore, the refractive index of the compound also has a certain value. The refractive index reflects its effect on the propagation characteristics of light, and may be of great significance in the research and application of optics.

The physical properties of 3 - amino -α,α,α - trifluorotoluene are rich and diverse, and the properties are interrelated, which plays a decisive role in its application in chemical synthesis, materials science and many other fields.

What are the chemical properties of 3-amino-alpha, alpha, alpha-trifluorotoluene

3 - amino - α,α,α - trifluorotoluene, this is an organic compound, commonly known as m-amino trifluorotoluene. It has special chemical properties and is important in the field of organic synthesis.

First talk about physical properties. This substance is mostly colorless to light yellow liquid at room temperature and has a special odor. The boiling point is about 187-188 ° C, the density is about 1.297g/cm ³, it is insoluble in water, but it is miscible with organic solvents such as ethanol and ether. This solubility makes it an excellent solvent or reaction medium in the construction of organic reaction systems, which can help the reactants to fully contact and accelerate the reaction process.

Re-discussion of chemical properties. Its amino group is nucleophilic and easily reacts with electrophilic reagents. For example, it can be acylated with acyl halides, acid anhydrides, etc., to form amide compounds. This reaction is commonly used in drug synthesis. By introducing different acyl groups, the biological activity and physical properties of the compound can be changed. At the same time, the amino group can be oxidized to form nitro or nitroso compounds, and the products are different under different conditions. It is widely used in the synthesis of fine chemicals.

And its α,α,α - trifluoromethyl, due to the large electronegativity of fluorine atoms, has a strong electron-absorbing induction effect. This reduces the electron cloud density of the benzene ring, decreases the electrophilic substitution reaction activity on the benzene ring, and selectively changes the reaction check point. Usually, the electrophilic substitution reaction is more likely to occur in the amino para-position, because the conjugation effect of the amino power supply is more significant in the para-position, which can partially cancel the electron-absorbing effect of trifluoromethyl.

In addition, trifluoromethyl also endows compounds with unique properties, such as improving fat solubility and enhancing the permeability of compound biofilms, which is of great significance in pesticide and pharmaceutical research and development, and often improves drug efficacy.

The chemical properties of 3 - amino - α,α,α - trifluorotoluene make it a key intermediate in many fields such as organic synthesis, pharmaceutical chemistry, and materials science, and can derive many high-value compounds.

What are the synthesis methods of 3-amino-alpha, alpha, alpha-trifluorotoluene

The synthesis of 3-amino -α,α,α - trifluorotoluene is a key issue in the field of organic synthesis. In the past, halogenated aromatics were mostly used as starting materials.

Initially, halogenated aromatics were taken and reacted with fluorinated reagents under suitable conditions to introduce trifluoromethyl. This step requires selecting appropriate fluorinated reagents, such as trifluoromethyl zinc halide, and controlling the reaction temperature, pressure and reaction time. Because the introduction of trifluoromethyl is challenging, the control of conditions is crucial.

Next, the halogenated aromatics containing trifluoromethyl were nitrified and nitro was introduced at a specific position in the benzene ring. In this process, the mixed acid of nitric acid and sulfuric acid is often a nitrifying reagent, and the temperature and reagent ratio need to be carefully adjusted to prevent excessive nitrification.

Then, the nitro group is converted into an amino group by reduction reaction. Commonly used reducing agents include iron/hydrochloric acid system, hydrogen/palladium carbon, etc. Although the iron/hydrochloric acid system is low cost, it is complicated to deal with; the hydrogen/palladium carbon system is relatively clean and efficient, but it requires high equipment and operation.

Another method is to introduce trifluoromethyl through a specific reaction path using an aromatic hydrocarbon containing amino groups as the starting material. This approach can avoid the problem of introducing trifluoromethyl first and then nitrifying, but it also has unique requirements for the acquisition of starting materials and reaction conditions. < Br >
There are also transition metal-catalyzed reaction strategies, through ligand design and reaction conditions optimization, to achieve the precise construction of trifluoromethyl and amino groups in benzene rings. This method has the advantages of high efficiency and good selectivity, but the high cost of catalysts limits its large-scale application. There are many methods for synthesizing 3-amino -α,α,α - trifluorotoluene, each with advantages and disadvantages, and the choice needs to be weighed according to actual needs and conditions.

What is the price range of 3-amino-alpha, alpha, alpha-trifluorotoluene in the market?

I have not heard the exact price of 3 - amino - α,α,α - trifluorotoluene in the market. However, if you want to know the price of this product, you can ask for it from many ways.

First, ask chemical raw material suppliers. There are many merchants specializing in chemical materials in the city. They always have various chemical products and are familiar with their prices. You can send or write to them, call them, and ask about the price of 3 - amino - α,α,α - trifluorotoluene.

Second, visit the chemical trading platform. In today's world, the network is developed, and there are many chemical trading platforms. On it, you can find the recent transaction price of this product, and you can compare the prices of different merchants to know its approximate range.

Third, refer to the chemical industry report. Professionals in the industry often write reports to record the market conditions of various chemicals, including the price changes and trends of 3-amino - α,α,α - trifluorotoluene, which can be referred to.

However, the price of this product often varies depending on quality, purity, purchase quantity, season, supply and demand. If you want a precise price, you must consult with the supplier according to actual needs. And the sale of chemicals, or involving regulations, qualifications and other matters, should also act in compliance.