2 Trifluoromethyl 4 Quinolinecarbonitrile
quinoline thiophene imidazole thiazole

2-(Trifluoromethyl)-4-quinolinecarbonitrile

Taiy Chemical

    Specifications

    HS Code

    532821

    Chemical Formula C11H5F3N2
    Molecular Weight 222.17
    Appearance Solid (usually powder or crystalline form)
    Physical State At Room Temperature Solid
    Melting Point Specific value would require experimental determination
    Boiling Point Specific value would require experimental determination
    Solubility In Organic Solvents May be soluble in some organic solvents like dichloromethane, DMSO etc., details need experimental study
    Solubility In Water Low solubility in water
    Purity Typical Range Varies depending on source and production method, could be >95% in high - quality samples
    Odor Typically odorless or with a faint, characteristic odor

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    Frequently Asked Questions

    As a leading 2-(Trifluoromethyl)-4-quinolinecarbonitrile 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 physical properties of 2- (trifluoromethyl) -4-quinolinocarbonitrile?
    In "Tiangong Kaiwu", triethyl-4-phenylacetamide is an organic compound, and its physical properties are particularly important.
    Under normal temperature, this substance is mostly solid, the texture may be crystalline, and the appearance is white like snow, with a certain luster, like natural jade, delicate and pure.
    Looking at its melting point, it is about a specific temperature range. This temperature makes it gradually melt from solid to liquid, just like ice disappearing under the warm sun. The characteristics of the melting point can help to distinguish its purity. If impurities are mixed, the melting point may be offset.
    Furthermore, its boiling point is also fixed. When the temperature rises to the boiling point, the substance suddenly changes from liquid to gaseous state. This process is widely used in chemical separation, purification and other fields. < Br >
    In terms of solubility, in some organic solvents, such as alcohols and ethers, it can dissolve well, just like fish entering water and blending freely; however, in water, the solubility is poor, just like oil floating in water, distinct. This property also provides the basis for its application in different media.
    In terms of density, there is a specific value, which is lighter or heavier than common substances, which determines its position in the mixture. For example, in a layered system, it can be located according to the density difference.
    In addition, its smell is weak, or it has a faint special smell, which is not pungent, but it is unique, like a unique logo hidden behind the scenes.
    In summary, the shape, melting point, boiling point, solubility, density, odor and other physical properties of triethyl-4-phenylacetamide are of key significance in many fields such as chemical industry and medicine, and lay the foundation for its synthesis, application, separation and other operations.
    What are the chemical properties of 2- (trifluoromethyl) -4-quinolinocarbonitrile
    The chemical properties of di- (trialkyl) -4-square photomethyl ether are quite specific.
    In this compound, the structure of the trialkyl methyl group gives the molecule a specific steric resistance. In the trialkyl methyl group, the length of the carbon chain and the branching situation of the alkyl group have an impact on the overall properties. Long-chain alkyl groups can increase the hydrophobicity of the molecule, and affect the interaction between molecules due to van der Waals forces. Its branching structure changes the shape of the molecule, which in turn affects the solubility and dispersion in different solvents.
    In the square photomethyl ether part, the methoxy group is connected to a specific aromatic ring structure, and the methoxy group is the power supply subgroup, which can change the density of the aromatic ring electron cloud. This change causes it to exhibit unique activities in electrophilic substitution reactions. For example, when electrophilic substitution occurs with halogenated hydrocarbons, the reaction check point is affected by the localization effect of methoxy groups, which mostly occurs in adjacent and para-positions.
    In terms of stability, in the molecule of di- (trialkyl) -4-square light methyl ether, each atom is connected by covalent bonds to form a relatively stable structure. However, under extreme conditions such as high temperature, strong acid or strong base, the covalent bond may be affected. For example, in a strong acid environment, the methoxy group may protonate, which then triggers the break of ether bonds; at high temperature, the trialkyl group may undergo thermal cracking reaction, which destroys the molecular structure.
    In terms of redox properties, aromatic ring parts can participate in the redox process if they are connected with suitable substituents. In case of strong oxidants, aromatic rings may be oxidized to form quinones or other oxidation products; under specific reduction conditions, aromatic rings can be hydrogenated and reduced, changing the degree of molecular unsaturation.
    In summary, di- (trialkyl methyl) -4 -square photomethyl ether exhibits various chemical properties in terms of solubility, reactivity, stability and redox properties due to its unique structure.
    What are the main uses of 2- (trifluoromethyl) -4-quinolinocarbonitrile?
    What is the main use of di- (trialkomethyl) -4-square light methyl ether? This is a question about the application of chemical materials. Today, in ancient Chinese, it will solve this doubt for you.
    Di- (trialkomethyl) -4-square light methyl ether is widely used in various fields of chemical industry. First, in the process of organic synthesis, it is often used as a key intermediate. Organic synthesis is exquisite, like a craftsman's artifact, every step needs to be precise. Due to its unique structure, this compound can participate in many reactions, paving the way for the synthesis of complex organic molecules. It can be cleverly combined with a variety of reagents, and through chemical reactions, various novel and useful organic products can be produced, just like a craftsman using different materials to create various exquisite utensils.
    Furthermore, in the field of medicinal chemistry, it also has important functions. Pharmaceutical research and development, such as exploring a good prescription for the world, requires careful consideration. This substance can help synthesize drug molecules with a specific structure. Because of its stable structure and certain reactivity, it can contribute to the construction of active pharmaceutical ingredients. The creation of some new drugs may find a breakthrough opportunity due to the participation of di- (trialkyl methyl) -4-square light methyl ether, which is like finding a glimmer of light in the dark, bringing hope for curing diseases.
    In addition, in the field of materials science, it also has its uses. The quality of materials is related to the development of many industries. This compound can be used to prepare materials with special properties. For example, the modification of some polymer materials, adding an appropriate amount of di- (trialkyl methyl) -4-square light methyl ether can improve the physical properties of the material, such as flexibility and stability, as if injecting vitality into the material, making it more suitable for different environments and application needs, and playing a greater role in industrial production and daily applications.
    What is the synthesis method of 2- (trifluoromethyl) -4-quinolinocarbonitrile?
    To prepare di- (triethyl) -4 -square photoacetamide, the method is as follows:
    First take an appropriate amount of starting materials, take the preparation of triethyl as an example, often need to select the corresponding carbon chain and functional group compounds, in a suitable reaction vessel, add specific catalysts, such as metal salts or organic bases. Control the reaction temperature and pressure, so that the reactants are fully contacted and chemical reactions occur. The temperature should be maintained in a specific range, and the pressure needs to be precisely regulated, so that the reaction can proceed in the direction of generating triethyl methyl. After the reaction is completed, the pure triethyl is obtained through the separation and purification steps.
    As for the preparation of 4-square photoacetamide, select a suitable photoethyl group compound and match it with an appropriate reaction reagent. Follow a specific reaction mechanism, either nucleophilic substitution or additive condensation. During the reaction process, strictly control the reaction conditions, such as temperature, pH, etc. Too high or too low temperature may affect the reaction rate and product purity; improper pH will also cause the reaction to deviate from the expected path. After the reaction is completed, pure 4-square photoacetamide is obtained by distillation, recrystallization and other means.
    Finally, the obtained triethylmethyl and 4-square photoacetamide are added to another reaction system. According to the chemical properties of the two, a suitable coupling agent or initiator is added to control the reaction conditions again, so that the coupling reaction occurs, and then the target product di- (triethylmethyl) -4-square photoacetamide is generated. After the reaction is completed, the product with high purity is obtained through fine separation and purification. The whole synthesis process requires careful operation by the experimenter and precise control of each reaction link in order to achieve the expected synthesis goal.
    What are the precautions for 2- (trifluoromethyl) -4-quinolinocarbonitrile in storage and transportation?
    In the storage and transportation of di- (Sanxiang methyl) -tetra- square light methyl decyl, many key matters need to be paid attention to.
    These two properties are quite unique. During storage, the temperature and humidity of the first environment are regulated. Its properties are quite sensitive to temperature changes. If the temperature is too high, it may cause qualitative changes or even cause dangerous reactions. Therefore, it should be stored in a cool place, so that the temperature is constant in a suitable range to prevent deterioration. And the humidity should not be underestimated. If the humidity is too high, it is easy to cause substances to get damp, which affects their purity and quality. Therefore, it is necessary to ensure that the storage environment is dry, and it can be maintained dry with the help of desiccants and other substances.
    Furthermore, the storage place should be well ventilated. These two may evaporate special gases. If the ventilation is not smooth and the gas accumulates, one may affect the properties of the substance itself, and the other may pose a threat to the surrounding environment and personal safety. At the same time, it must be strictly isolated from other chemical substances. Because of its active chemical properties, contact with certain substances, or cause severe chemical reactions, such as explosion, combustion and other serious consequences.
    When transporting, the packaging must be solid and stable. Appropriate packaging materials need to be selected to ensure that the substance does not leak in the case of bumps, collisions, etc. And the transportation vehicle should also meet specific requirements and have perfect protective and emergency equipment. Transport personnel must be professionally trained and familiar with the characteristics of these two and emergency treatment methods. Transportation route planning is also crucial, and densely populated areas and environmentally sensitive areas should be avoided to prevent accidents during transportation and cause harm to the public and the environment. In short, the storage and transportation of di- (Sanxiang methyl) -tetragonal methyl decyl requires careful attention to every detail to ensure safety.