2 Chloro 5 Trifluoromethyl Pyridine
pyridine pyrrole pyrazine piperidine piperazine

2-Chloro-5-(trifluoromethyl)pyridine

    Specifications

    HS Code

    634966

    Chemical Formula C6H3ClF3N
    Molecular Weight 181.54
    Appearance Typically a colorless to pale yellow liquid
    Boiling Point Around 145 - 147 °C
    Density Data varies, around 1.4 g/cm³
    Solubility In Water Low solubility in water
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane
    Flash Point Data may vary, but generally flammable
    Odor May have a pungent or characteristic odor
    Cas Number 1484-77-3

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    Frequently Asked Questions

    As a leading 2-Chloro-5-(trifluoromethyl)pyridine supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What are the main uses of 2-chloro-5- (trifluoromethyl) pyridine?
    2-% -5- (triethylmethyl) pyridine, which is a valuable chemical compound, its main use is wide.
    In the field of chemical synthesis, it is often used as an important chemical compound in synthesis. Due to the specialization of chemical compounds, it can be skillfully modified by available synthetic methods, and many chemical molecules with specific biological activities can be produced. For example, some novel chemical compounds used to treat specific diseases, in their synthesis pathway, 2-% -5- (triethylmethyl) pyridine is used as a starting material or medium material, and the most ideal chemical activity is obtained.
    In the field of materials science, it also plays an important role. Functional materials with specific properties can be synthesized. For example, in the research of some optical materials, the introduction of this compound element can effectively control the properties of the material, such as the properties of the material, the properties of the light, etc., so as to improve the properties of the material, such as the properties of the light, etc., and meet the special needs of the field of optical devices.
    In addition, in the basic field of chemical research, 2-% -5- (triethylmethyl) pyridine is also commonly used as a chemical reaction or a catalytic reaction. Due to its properties, it can be used in many chemical reactions, or directly in the chemical reaction, and the construction of specific chemical reactions; or as a fixed catalytic activity center, improve the efficiency of the catalytic reaction, and help the chemical industry to explore new and efficient synthetic methods.
    What are the physical properties of 2-chloro-5- (trifluoromethyl) pyridine?
    2-% -5- (triethylmethyl) pyridine, this is an organic compound. Its physical properties are quite unique, let me tell you one by one.
    Looking at its properties, under room temperature and pressure, it is mostly in the form of a colorless to pale yellow liquid, just like clear water, but contains unique properties. It shines softly in the sun, as if it hides an unknown mystery.
    Smelling its smell, it exudes a special aroma, neither rich and pungent, nor elegant and tasteless, but unique and impressive, like a unique gift from a distant and mysterious place. < Br >
    When it comes to boiling point, it is within a certain temperature range, which causes the substance to transform from liquid to gas. When heated to a specific temperature, the surface of the liquid will churn violently, and a large number of bubbles will gush out, turning into steam and rising. The melting point also has its specific value. Under the corresponding low temperature conditions, the substance will solidify from liquid to solid state, as if frozen in time, showing a different solid state.
    In terms of solubility, it exhibits good solubility in some organic solvents, such as alcohols, ethers and other organic solvents, as if it can be integrated with these solvents, regardless of each other, to form a uniform mixing system; however, the solubility in water is relatively limited, the two meet, like oil and water, it is difficult to completely blend, only a small amount of dissolution, forming a delicate balance.
    In terms of density, compared with water, it has a specific value, which makes it when mixed with other substances such as water, it will show different distribution states according to the density difference, either floating on water or sinking underwater, showing the wonderful interaction between substances.
    In summary, the physical properties of 2-% -5- (triethylmethyl) pyridine are rich and diverse, which not only determine its performance in chemical reactions, but also affect its application in many fields such as industry and scientific research. It is a substance worthy of further investigation.
    What are the chemical properties of 2-chloro-5- (trifluoromethyl) pyridine?
    2-% -5- (trimethyl) pyridine is a compound containing special properties. Its chemical properties are special, let me describe.
    First of all, the atom in this compound, due to its chemical properties, can be diversified and reversed. The activity of the atom is to a certain extent affected by the influence of the pyridol group. At the 2-position, the atom can be used as a carrier to provide a carrier, an acid, and a carrier. It is easy to remove the carrier and generate the carrier of the phase.
    Furthermore, the introduction of the 5- (trimethyl) pyridine moiety, trimethyl groups, has changed the molecular composition of the pyridol. The methyl group is used to provide a daughter group, which can increase the density of the sub-cloud on the pyridine, especially in the high and low positions of the pyridine. This change in the density of the sub-cloud results in the generation of the anti-substitution and anti-activity of the pyridine. Compared with the unsubstituted pyridine, this compound is more likely to generate the anti-substitution and anti-substitution, and the anti-location is often the location where the density of the sub-cloud increases.
    The same, the effect of trimethyl can not be ignored. Its empty-site barrier affects the interaction of the molecules and the way of the reaction. In some reactions, the trimethyl group of the large potential barrier may prevent some of the molecules from approaching the pyridine, making the reaction.
    In addition, the nitrogen atom of this compound has solitary ions, which gives it a certain property. The property of the nitrogen atom can make it react to acid and form a compound. This property also affects its role in the synthesis of chemical compounds, and can be used as a catalyst or a catalyst, and a catalyst for the reaction of gold.
    In addition, the chemical properties of 2-5- (trimethyl) pyridine are rich, and the interaction of its atom, pyridine and trimethyl groups determines its activity. It has important research capabilities in the fields of chemical synthesis, physicochemistry, and so on.
    What are the synthesis methods of 2-chloro-5- (trifluoromethyl) pyridine?
    To prepare 2-cyanogen-5- (trifluoromethyl) pyridine, there are many methods, each has its own advantages and disadvantages, and is suitable for different scales and scenarios. The following are common methods:
    ** 1. Pyridine derivatives are used as starting materials **
    1. ** Halogenated pyridine method **
    Select suitable halogenated pyridine, such as 2-halogenated-5- (trifluoromethyl) pyridine, and react with cyanide reagents. Copper cyanide (CuCN) is commonly used in cyanide reagents, and it is heated and stirred in a suitable organic solvent, such as N, N-dimethylformamide (DMF). This reaction requires a strict anhydrous and oxygen-free environment, because cuprous cyanide is easily decomposed in contact with water, affecting the yield. The reaction process is nucleophilic substitution, and the halogen atom is replaced by a cyano group. The advantage is that the raw material is relatively easy to obtain and the route is direct; the disadvantage is that cuprous cyanide is highly toxic, the operation needs to be cautious, and the reaction conditions are harsh. The post-treatment is complicated, and excess cuprous cyanide and by-products must be removed.
    2. ** Pyridine boronic acid method **
    2-boronic acid-5- (trifluoromethyl) pyridine reacts with cyanation reagents, such as trimethylsilyl cyanide (TMSCN), under the action of transition metal catalysts (such as palladium The reaction is carried out under mild conditions, and toluene or dichloromethane are commonly used in organic solvents. This reaction is catalyzed by transition metals to form carbon-cyanide bonds. The advantage is that the reaction conditions are mild and the yield is high; the disadvantage is that the cost of palladium catalysts is high, and recovery needs to be considered. And trimethylsilyl cyanide has certain toxicity and volatility, and the operation needs to be well ventilated.
    * Second, the method of constructing a pyridine ring **
    1. ** Using β-dicarbonyl compounds as raw materials **
    Cyclization and condensation of β-dicarbonyl compounds containing trifluoromethyl groups with cyanide-containing amination reagents, such as cyanoacetamide, under the action of acidic or basic cataly P-toluenesulfonic acid is commonly used in acidic conditions, and sodium ethyl alcohol can be selected in alkaline conditions. First condensation forms an intermediate product, and then dehydration and aromatization obtain the target product. This route is simple in raw materials and low in cost; but the reaction steps are many, and the reaction conditions of each step need to be strictly controlled. The total yield is affected by the multi-step reaction, and the reaction process is complex, and there are many side reactions, which make it difficult to separate and purify.
    2. ** Using the heterocyclic synthesis method **
    to construct a pyridine ring with a suitable small molecule containing fluorine and cyano groups through a multi-step reaction. Such as cyclization under specific conditions by enamines and nitriles. This method is highly flexible and can design reaction routes on demand; but the steps are complicated, requiring professional organic synthesis knowledge and technology, and demanding high reaction equipment and operation. It is suitable for laboratory research or preparation of special structure pyridine derivatives.
    What are the precautions for using 2-chloro-5- (trifluoromethyl) pyridine?
    In the case of 2-% -5- (triethylmethyl) pyridine, there are many things to pay attention to when using it, which cannot be ignored.
    This material property is special. First of all, it contains specific groups in its chemical properties, which makes it sensitive to environmental factors. In the case of moisture, it is easy to produce hydrolysis, so it needs to be properly stored in the dry environment, and the dense container should be protected from moisture. If the substance is damp, not only its activity is reduced, but also harmful by-products may be generated, endangering the safety of the user.
    Furthermore, the reaction of other substances also needs to be paid attention to. This pyridine has some gold particles that meet, or combine and react, changing the properties of the substance. When it is compatible with other materials, it is necessary to study the chemical properties of the two before they can be used together. If it is not effective, it will reduce the effect, re-induce the strong chemical reactions, and cause serious problems.
    It is important to control the amount of energy used. This effect is affected, but if it is used in excess, it will cause toxic and side effects. It can cause diseases such as heart disease and heart disease, and it can affect the function of organs such as liver and liver. Therefore, when using it, the amount must be controlled according to the instructions of the person, and the amount should not be increased without authorization.
    In addition, the user's behavior also has an impact. Different people, the tolerance of this product is different. Some people may not have the appearance of sensitivity, and it is advisable to make skin sensitivity before use. If there is a history of sensitivity, it is especially necessary to be careful to ensure safety.
    Therefore, 2-% -5- (triethylmethyl) pyridine has a certain effect, but the use of it requires careful attention in terms of storage, compatibility, quantity, and user awareness, so as to ensure the safety and effectiveness of use.