2 Amino 5 Chlorobenzotrifluoride
Fluoride
2-amino-5-chlorobenzotrifluoride
Chemical Formula C7H5ClF3N
Molecular Weight 195.57
Appearance Typically a colorless to light - yellow liquid
Boiling Point Approximately 203 - 205 °C
Density Around 1.38 g/cm³
Solubility Slightly soluble in water, soluble in organic solvents like ethanol, ether
Vapor Pressure Low vapor pressure at normal conditions
Flash Point Relatively high flash point, around 85 °C
Odor May have a characteristic, pungent odor
FAQ

What are the main uses of 2-amino-5-chlorotrifluorotoluene?

2-% hydroxy-5-bromotrifluorotoluene, which is a crucial raw material in organic synthesis, is widely used in many fields.

In the field of medicinal chemistry, it plays a crucial role. With its special chemical structure, it can be used as a key intermediate for the synthesis of a variety of specific drugs. For example, in the development of some new drugs with antiviral and antitumor activities, 2-hydroxy-5-bromotrifluorotoluene can be ingeniously introduced into the molecular structure of the drug through a series of chemical reactions, endowing the drug with unique biological activity and pharmacological properties, helping to improve the therapeutic effect of the drug on specific diseases, and making great contributions to human health. < Br >
is also indispensable in the field of materials science. It can be used as an important structural unit in the preparation of high-performance organic optoelectronic materials. Because of its fluorine, bromine and other special atoms, it can effectively adjust the electron cloud distribution and intermolecular forces of materials, thereby optimizing the photoelectric properties of materials. The organic optoelectronic materials synthesized on this basis can be widely used in cutting-edge fields such as organic light emitting diodes (OLEDs) and solar cells to promote the progress and innovation of related technologies, and improve the key performance indicators such as luminous efficiency, stability and photoelectric conversion efficiency of materials.

In the field of pesticide chemistry, it also shows extraordinary value. Can be used to create new and efficient pesticides. With their chemical properties, synthetic pesticides are highly selective and highly lethal to specific pests or pathogens, and may have lower toxicity and better environmental compatibility than traditional pesticides, contributing to the green and sustainable development of agriculture, ensuring crop yield and quality, and reducing the negative impact of pesticides on the ecological environment.

What are the physical properties of 2-amino-5-chlorotrifluorotoluene?

2-% amino-5-bromotrifluorotoluene is an important compound in the field of organic chemistry. Its physical properties are unique, so let me explain in detail.

Looking at its appearance, under normal temperature and pressure, it is mostly colorless to light yellow liquid, with a clear texture. Under sunlight, it may appear slightly shiny, as if it hides endless chemical mysteries. It has a special smell, although it is difficult to describe accurately, it is distinct and unique. Experienced chemical practitioners may be able to initially identify this compound by this smell.

Talking about the melting point and boiling point, this substance has a low melting point and is difficult to be solid under the temperature of ordinary experimental environments. The boiling point varies slightly according to specific conditions, and is roughly in a certain temperature range. This characteristic makes it subject to specific conditions in distillation, separation and other operations. The existence of the boiling point indicates the energy required to convert from liquid to gaseous state, which is an important factor to be considered in chemical operations.

In terms of solubility, 2-% amino-5-bromotrifluorotoluene exhibits good solubility in many organic solvents, such as common ethanol, ether, dichloromethane, etc. This solubility provides great convenience in organic synthesis reactions. Many reactions need to be carried out in a solution environment. Its good solubility allows the reactants to be fully contacted, accelerating the reaction process and improving the reaction efficiency. However, in water, its solubility is poor, which is also a significant characteristic related to water.

Density is also one of the important physical properties of this compound. Compared with water, its density may be different, and it will occupy a specific position in the mixed system due to density differences. This property has important application value in mixture separation, extraction and other operations. Knowing its density allows chemists to more accurately plan the experimental process and achieve the expected experimental goals.

The physical properties of 2-% amino-5-bromotrifluorotoluene, from appearance and odor to melting and boiling point, solubility and density, are the key basis for the research and application of organic chemistry, laying a solid foundation for in-depth exploration in related fields.

What are the chemical properties of 2-amino-5-chlorotrifluorotoluene?

The chemical properties of 2-% hydroxy-5-bromotrifluorotoluene are particularly important and are related to many chemical synthesis and related applications.

This compound has certain stability, but under specific conditions, its hydroxyl and bromine atoms can exhibit active reactivity. Hydroxyl groups can participate in esterification reactions. When encountering carboxylic acids or their derivatives, under suitable catalysts and reaction conditions, corresponding ester compounds can be formed. This reaction is often used in organic synthesis to construct specific structural units and endow the product with new physical and chemical properties.

Furthermore, its bromine atoms are also quite active. In nucleophilic substitution reactions, bromine atoms can be replaced by various nucleophilic reagents. In case of reagents containing nitrogen, oxygen, sulfur and other nucleophilic atoms, substitution can occur, thus introducing different functional groups, which greatly enriches the structure and function of the compound.

The existence of trifluoromethyl has a great impact on the properties of the compound. Trifluoromethyl is a strong electron-absorbing group, which can change the electron cloud density distribution of the molecule, which in turn affects the polarity and acidity of the compound. Due to the strong electron-absorbing effect of trifluoromethyl, the acidity of the hydroxyl group is enhanced, and it is easier to give protons in some reactions.

At the same time, the physical properties of the compound cannot be ignored. Its solubility is affected by various groups in the molecular structure. In organic solvents, due to the hydrophobicity of trifluoromethyl, it has good solubility in some non-polar or weakly polar organic solvents, but relatively poor solubility in water.

In terms of selectivity in chemical reactions, the reaction often exhibits specific selectivity due to the electronic and spatial effects of different functional groups in the molecule. For example, in some complex reaction systems, hydroxyl and bromine atoms will preferentially participate in different reaction paths due to differences in reaction conditions, providing rich strategic options for organic synthesis.

What are the synthesis methods of 2-amino-5-chlorotrifluorotoluene?

To prepare 2-amino-5-bromotrifluorotoluene, there are various methods.

First, it can be started with a suitable aromatic compound. The aromatic ring is first brominated so that the bromine atom reaches the desired 5 positions. This bromination step requires careful selection of brominating reagents and reaction conditions to maintain regioselectivity. Commonly used brominating agents such as liquid bromine, combined with appropriate catalysts such as iron or iron salts, can precisely occupy the bromine atom at a suitable temperature and reaction environment.

Afterwards, an amino group is introduced. Nitro groups can be introduced at the 2 position through nitration reaction, and then the nitro group can be converted to amino groups by reduction means. When nitrogenation, a mixed acid of concentrated nitric acid and concentrated sulfuric acid is selected, and the temperature and reaction time are adjusted according to the activity of the substrate to achieve the ideal regioselectivity. For the reduction of nitro groups, catalytic hydrogenation can be used, using palladium carbon as a catalyst, and hydrogen gas is introduced to achieve conversion; chemical reduction can also be used, such as iron powder, zinc powder, etc. to reduce nitro groups to amino groups in acidic media.

Second, fluorine-containing substrates can be used. Starting with an aromatic compound containing trifluoromethyl groups, an amino group is first introduced, and then brominated. The method of introducing amino groups can also pass nucleophilic substitution reactions in addition to the above-mentioned nitro reduction. If there are suitable leaving groups on the aromatic ring of the substrate, such as halogen atoms or sulfonate groups, they can react with ammonia or amine nucleophiles to introduce amino groups. In the subsequent bromination step, according to the characteristics of the substrate, the appropriate brominating agent and conditions are selected to achieve 5-position bromination.

Third, a coupling reaction strategy can also be used. The amino-containing and bromine-containing and trifluoromethyl-containing fragments are prepared first, and then the two are connected by palladium-catalyzed coupling reactions, such as Suzuki coupling, Stille coupling, etc. This strategy requires the appropriate functionalization of the fragment in advance, and the selection of suitable ligands and reaction conditions to improve the reaction efficiency and selectivity. Each method has its advantages and disadvantages. In the actual synthesis, the optimal method should be selected according to the comprehensive consideration of factors such as raw material availability, cost, reaction difficulty and product purity.

What should be paid attention to when storing and transporting 2-amino-5-chlorotrifluorotoluene?

2-%E6%B0%A8%E5%9F%BA-5-%E6%B0%AF%E4%B8%89%E6%B0%AF%E7%94%B2%E8%8B%AF are fine chemicals. When storing and transporting, many matters need to be paid attention to.

The first to bear the brunt, when storing, must choose a cool, dry and well-ventilated place. This is because the material is hot or wet, it may cause unstable changes, or cause quality damage, and even endanger safety. Cover high temperature can accelerate its chemical reaction, and moisture can easily lead to adverse reactions such as hydrolysis.

Furthermore, the storage place must be away from fire sources, heat sources and oxidants. 2-%E6%B0%A8%E5%9F%BA-5-%E6%B0%AF%E4%B8%89%E6%B0%AF%E7%94%B2%E8%8B%AF flammable, in case of fire or hot topic, it will explode instantly, causing harm to the surroundings; when it encounters with oxidants, it is easy to trigger violent reactions, which is dangerous.

As for the transportation, the packaging must be solid and sealed. To prevent it from leaking due to bumps and collisions on the way. Leakage not only stains the environment, but also causes disasters such as poisoning and fire due to the characteristics of the substance. And the means of transportation must also be clean, dry, and free of other chemicals to avoid cross-contamination and chemical reactions with it.

The escort should be familiar with the characteristics of 2-%E6%B0%A8%E5%9F%BA-5-%E6%B0%AF%E4%B8%89%E6%B0%AF%E7%94%B2%E8%8B%AF and emergency response methods. If there is any abnormality on the way, deal with it immediately and properly. If there is a leak, evacuate the crowd immediately, isolate the scene, and choose the appropriate method according to its characteristics. In this way, the storage and transportation are guaranteed to be safe and safe, so as to avoid disasters.