3 Trifluoromethyl 2 Pyridinecarboxaldehyde
pyridine pyrrole pyrazine piperidine piperazine

3-Trifluoromethyl-2-pyridinecarboxaldehyde

    Specifications

    HS Code

    786044

    Chemical Formula C7H4F3NO
    Molecular Weight 175.11
    Appearance Typically a colorless to light yellow liquid
    Boiling Point Specific value would require further research
    Melting Point Specific value would require further research
    Solubility Solubility characteristics in common solvents like water, ethanol, etc. would need research
    Density Specific density value would need determination
    Flash Point Specific flash point value would require testing
    Vapor Pressure Value depends on temperature, needs experimental data
    Pka Acidity constant data would need research

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    Frequently Asked Questions

    As a leading 3-Trifluoromethyl-2-pyridinecarboxaldehyde supplier, we deliver high-quality products across diverse grades to meet evolving needs, empowering global customers with safe, efficient, and compliant chemical solutions.

    What is the chemistry of 3-Trifluoromethyl-2-pyridinecarboxaldehyde?
    3-Trifluoromethyl-2-pyridyl formaldehyde, an organic compound with unique chemical properties. Its appearance is often colorless to pale yellow liquid or solid, and it is widely used in the field of organic synthesis and is a key intermediate.
    From the perspective of chemical activity, aldehyde groups are active and easy to participate in a variety of reactions. If they can be acetalized with alcohols to generate acetals, this reaction can be used to protect aldehyde groups in organic synthesis, and then deprotected at a specific stage to accurately achieve the construction of target molecules. It can also carry out oxidation reaction, aldehyde group is easily oxidized to carboxyl group, select suitable oxidants, such as potassium permanganate, potassium dichromate, etc., can achieve this conversion, and obtain 3-trifluoromethyl-2-pyridinecarboxylic acid. The product has important applications in medicine, pesticides and other fields.
    Furthermore, due to the existence of pyridine ring and trifluoromethyl group, the molecule has a unique electronic effect and spatial structure. Trifluoromethyl group has strong electron absorption, which will affect the distribution of the electron cloud of the pyridine ring, and change the check point and activity of the electrophilic substitution reaction on the pyridine ring. Usually, the electrophilic substitution reaction is more likely to occur at the relatively high density of the electron cloud of the pyridine ring, which provides a basis for the synthesis of At the same time, the introduction of trifluoromethyl can improve the fat solubility of compounds, which affects their biological activity, stability and other properties. In drug development, it is often used to optimize the performance of lead compounds.
    In addition, 3-trifluoromethyl-2-pyridyl formaldehyde can also participate in condensation reactions with amines to generate Schiff bases. Such reaction products also have important applications in catalysis, materials science and other fields. In short, its diverse chemical properties make it a key position in many fields such as organic synthesis, medicinal chemistry, and materials science, laying the foundation for the creation of novel compounds and materials.
    What are the main uses of 3-Trifluoromethyl-2-pyridinecarboxaldehyde?
    3-Trifluoromethyl-2-pyridine formaldehyde, this substance has a wide range of uses. In the field of pharmaceutical synthesis, it is often a key intermediate. Due to the structure of pyridine containing trifluoromethyl, it has unique biological activity and physicochemical properties in many drug molecules. With this aldehyde group, it can be combined with other compounds through various chemical reactions to build complex drug molecular structures for the development of antibacterial, antiviral and anti-tumor drugs.
    It is also useful in the field of materials science. It can be introduced into polymer materials through specific reactions. Due to the strong electronegativity and unique electronic effects of trifluoromethyl, the properties of the materials can be improved, such as improving the thermal stability, chemical stability and electrical properties of the materials, and then applied to the preparation of special functional materials.
    In the field of organic synthetic chemistry, as an active aldehyde compound, 3-trifluoromethyl-2-pyridyl formaldehyde can participate in many classic organic reactions, such as the condensation reaction between aldehyde and amine, and the acetal reaction with alcohols. It provides an effective way for the synthesis of various nitrogen-containing and oxygen-containing heterocyclic compounds, greatly enriching the variety of organic compounds, and contributing to the development of organic synthetic chemistry.
    What is 3-Trifluoromethyl-2-pyridinecarboxaldehyde synthesis method?
    To prepare 3-trifluoromethyl-2-pyridine formaldehyde, the following method is often followed.
    First, 3-trifluoromethyl-pyridine is taken as the starting material. To introduce an aldehyde group to its 2-position, the Vilsmeier-Haack reaction can be used. In this reaction, N, N-dimethylformamide (DMF) and phosphorus oxychloride (POCl) are used as reagents. First, DMF interacts with POCl to form an active Vilsmeier reagent. The phosphorus atom in this reagent has strong electrophilicity and can be electrophilically substituted with the 2-position of 3-trifluoromethyl-pyridine. The nitrogen atom of the pyridine ring has a lone pair of electrons, which makes the electron cloud density distribution uneven on the ring, and the 2-position is relatively electron-rich, which is conducive to the attack of electrophilic reagents.
    During the reaction, 3-trifluoromethyl pyridine is slowly added to the mixed solution containing DMF and POCl
    . At an appropriate temperature, it is usually heated and refluxed to make the reaction fully proceed. At this time, the active part of the Vilsmeier reagent is connected to the 2-position carbon of pyridine to form an intermediate. Then, through the hydrolysis step, this intermediate is converted into the target product 3-trifluoromethyl-2-pyridine formaldehyde. During hydrolysis, the reaction mixture is usually treated with water or alkaline aqueous solution, and the phosphorus-carbon bond in the intermediate is broken and the aldehyde group is formed.
    After the reaction is completed, the product needs to be separated and purified. Because the reaction system may contain unreacted raw materials, by-products and solvents, it can be extracted with an organic solvent first, combined with organic phases, and then distilled under reduced pressure to separate the target product 3-trifluoromethyl-2-pyridine formaldehyde using the difference in boiling points of each component to obtain a pure product.
    3-Trifluoromethyl-2-pyridinecarboxaldehyde What are the precautions during storage and transportation?
    3-Trifluoromethyl-2-pyridyl formaldehyde is an organic compound, and many things must be paid attention to when storing and transporting.
    When storing, the first environment is heavy. A dry, cool and well-ventilated place should be selected, because the compound may be sensitive to humidity and temperature. If the environment is humid, it may cause moisture absorption and deterioration; if the temperature is too high, it may cause chemical reactions and damage the quality. Furthermore, it must be kept away from fire sources and oxidants. Because of its flammability, it is at risk of burning in case of open flames, hot topics or; and contact with oxidants, it is easy to react violently and cause danger. When storing, it should be packed in a sealed container to prevent volatilization and leakage, and at the same time, it should be tightly sealed to prevent air from entering and oxidizing it.
    During transportation, it should not be taken lightly. Be sure to ensure that the packaging is intact to prevent vibration and collision from causing the package to break and leak. The means of transportation should be clean, dry, and free of combustibles, oxidants, and other incompatible substances. Transport personnel should be familiar with the characteristics of the compound and emergency treatment methods. In case of leakage, they can dispose of it quickly and properly. And the transportation process should avoid high temperature periods and areas to slow down the possible chemical reaction rate. In short, the storage and transportation of 3-trifluoromethyl-2-pyridine formaldehyde should be handled with caution and strictly abide by relevant regulations to ensure the safety of personnel and the quality of goods.
    What is the market price range for 3-Trifluoromethyl-2-pyridinecarboxaldehyde?
    The market price range of 3-trifluoromethyl-2-pyridyl formaldehyde is difficult to determine. The price of this compound in the chemical materials market varies due to multiple factors.
    First, the complexity of the production process has a great impact. If the preparation requires fine steps, special raw materials or harsh conditions, the cost will be high, and the price will also rise.
    Second, the purity requirement is the key factor. High-purity products are much more expensive than ordinary purity products due to the difficulty of purification. Scientific research uses often require high purity and the price is high; if the purity requirements are slightly lower in industrial production, the price may be relatively easy.
    Third, the market supply and demand relationship determines the price. If the demand is strong and the supply is limited, the price will rise; if the supply exceeds the demand, the price will stabilize or decline.
    Fourth, the cost of raw materials also plays a role. The difficulty of obtaining raw materials and price fluctuations are directly related to the cost and selling price of products.
    Looking at the past chemical market conditions, similar fine chemical prices fluctuate violently. Ordinary purity, per gram or dozens of yuan; high purity and high quality, per gram can reach hundreds of yuan or even higher. However, this is only a rough guess, and the actual price must be determined comprehensively according to the current market conditions, transaction quantity, supplier differences, etc. To know the exact market price, please consult the chemical raw material supplier or research on the relevant professional trading platform.