Methyl 4 Trifluoromethyl Pyridine 2 Carboxylate
pyridine pyrrole pyrazine piperidine piperazine

Methyl 4-(trifluoromethyl)pyridine-2-carboxylate

    Specifications

    HS Code

    954394

    Chemical Formula C8H6F3NO2
    Molar Mass 205.13 g/mol
    Appearance Typically a colorless to pale - yellow liquid or solid
    Boiling Point Data may vary, but around a certain temperature (specific value would need more research)
    Melting Point Also data - specific, may be in a certain range
    Solubility Solubility characteristics in different solvents like organic solvents (e.g., slightly soluble in water, more soluble in common organic solvents like ethanol, dichloromethane)
    Density Some density value (needs accurate determination)
    Vapor Pressure Value dependent on temperature, relevant for volatility assessment
    Flash Point A temperature indicating flammability risk
    Stability Stable under normal conditions, but may react with strong oxidizing agents

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    Frequently Asked Questions

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    What is the main use of Methyl 4- (trifluoromethyl) pyridine-2-carboxylate?
    Methyl 4- (trifluoromethyl) pyridine - 2 - carboxylate, Chinese name methyl 4- (trifluoromethyl) pyridine - 2 - carboxylate, this is an important intermediate commonly used in the field of organic synthesis.
    It has a wide range of uses and is often the key raw material for the synthesis of various biologically active drugs in the field of pharmaceutical chemistry. Due to the unique properties of the structure of pyridine and trifluoromethyl, the drugs prepared with this intermediate may have good biological activity, membrane permeability and metabolic stability. For example, in the synthesis path of some innovative drugs used to treat specific diseases, methyl 4- (trifluoromethyl) pyridine - 2 - carboxylate can introduce key structural fragments through specific reaction steps to help build molecular architectures with precise pharmacological effects.
    In the field of materials science, it also has important uses. It can participate in the synthesis of functional organic materials, such as materials for the preparation of specific photoelectric properties. Due to the strong electron absorption of trifluoromethyl, or the electron cloud distribution of the material can be adjusted, which in turn affects its optical and electrical properties, it is used to manufacture organic Light Emitting Diodes (OLEDs), solar cells and other materials to improve the performance of related devices.
    In addition, in the field of pesticide chemistry, pesticides synthesized from this intermediate may have the characteristics of high efficiency, low toxicity and environmental friendliness. Its special structure helps to enhance the effect of pesticides on target organisms, while reducing the impact on non-target organisms, in line with the trend of modern pesticide development.
    Methyl 4- (trifluoromethyl) pyridine-2-carboxylate
    There are many ways to synthesize methyl 4- (trifluoromethyl) pyridine-2 -carboxylic acid esters, and the advantages and disadvantages of each method are mutual. The choice of the best one depends on the specific situation.
    One method can be made of 4- (trifluoromethyl) pyridine-2 -carboxylic acid and methanol, using concentrated sulfuric acid as a catalyst, esterification reaction under heating and reflux state. The raw materials in this way are easy to obtain, but the concentrated sulfuric acid is highly corrosive, the post-treatment is complicated, and the reaction conditions are harsh, requiring fine temperature control.
    Another method, using 4- (trifluoromethyl) pyridine-2-formyl chloride and methanol as materials, and pyridine as acid binding agent, the two react in a mild environment to obtain the target product. This reaction is mild and the yield is quite high. However, the activity of formyl chloride is high, and the preparation and storage need to be cautious. Pyridine has a poor odor and is also short.
    Another route, using 4- (trifluoromethyl) pyridine-2-nitrile as the starting material, is first hydrolyzed to obtain carboxylic acid, and then esterified with methanol. This step is slightly complicated, and the nitriles are relatively stable and easy to operate. If the raw material nitriles are easily available, it is a feasible method.
    In addition, it can also be achieved by coupling reactions catalyzed by transition metals. For example, halogenated pyridine containing corresponding substituents is coupled with reagents containing carboxyl groups or their derivatives under the action of metal catalysts such as palladium and copper, and then the construction of target molecules is completed. Such methods have excellent selectivity and can precisely bond in complex systems. However, the cost of catalysts is high, the reaction conditions are also harsh, and the requirements for reaction equipment and operation technology are very high.
    When synthesizing methyl 4- (trifluoromethyl) pyridine-2-carboxylate, it is necessary to comprehensively consider many factors such as raw material cost, reaction conditions, equipment requirements, product purity and yield, and carefully select the appropriate synthesis path.
    What are the physical and chemical properties of Methyl 4- (trifluoromethyl) pyridine-2-carboxylate
    Methyl 4- (trifluoromethyl) pyridine-2-carboxylic acid ester is one of the organic compounds. Its physicochemical properties are particularly important and are related to many chemical and chemical applications.
    Looking at its physical properties, under normal temperature and pressure, this compound is often in a liquid state. Due to the specific situation of intermolecular forces, it is in such an aggregated state. Its boiling point is also a key physical parameter, about a specific temperature range. This temperature allows the molecule to be energized enough to overcome the attractive forces between molecules and transition from the liquid state to the gaseous state.
    When it comes to solubility, methyl 4- (trifluoromethyl) pyridine-2-carboxylate has good solubility in organic solvents such as ethanol and ether. This is due to the formation of suitable interactions between the molecular structure and the molecules of organic solvents, such as van der Waals forces, hydrogen bonds, etc. However, in water, its solubility is poor, and it is difficult to form effective interactions with water molecules due to the hydrophobicity of trifluoromethyl groups in its molecules.
    As for the chemical properties, the ester groups can undergo hydrolysis. In contact with water and under appropriate acid-base catalysis conditions, the ester groups break to form corresponding carboxylic acids and alcohols. Under acidic conditions, the hydrolysis is reversible; under basic conditions, the hydrolysis is complete. < Br >
    And because of the existence of the pyridine ring, it has a certain alkalinity. The solitary pair electrons on the nitrogen atom of the pyridine ring can accept protons, and can form pyridine salts in acidic environments. This basic property makes the compound able to participate in many acid-base related chemical reactions. And the strong electron-absorbing properties of trifluoromethyl affect the electron cloud distribution of the pyridine ring, which in turn affects its reactivity and selectivity, which are reflected in nucleophilic substitution, electrophilic substitution and other reactions.
    What is the price of Methyl 4- (trifluoromethyl) pyridine-2-carboxylate in the market?
    I look at this question, but I am inquiring about the market price of "Methyl 4- (trifluoromethyl) pyridine - 2 - carboxylate". Sadly, I have not covered the price of this item in "Tiangong Kaiwu", and the market price often varies with time, place, quality, quantity and supply and demand, so it is difficult to determine. However, if you want to know the price, you can visit the chemical raw material trading market and online chemical product platform, consult suppliers, and study the quotations of each source in detail to get a more accurate price. Or you can participate in industry exhibitions and seminars, and communicate with people in the industry to explore the price. And the price of chemical raw materials is disturbed by policies, costs, etc. It is advisable to check the industry information to clarify the price trend. Although I have not been able to tell the price directly, I hope this path can help you get the price you need.
    What are the storage conditions for Methyl 4- (trifluoromethyl) pyridine-2-carboxylate?
    Methyl 4- (trifluoromethyl) pyridine-2-carboxylic acid ester is a kind of organic compound. Its storage conditions are related to the stability and quality of this substance, which cannot be ignored.
    According to the principles of "Tiangong Kaiwu", the properties of the substance need to be considered. Methyl 4- (trifluoromethyl) pyridine-2-carboxylic acid ester should be stored in a cool place. It is easy to increase molecular activity due to heat, or the risk of decomposition and deterioration. Therefore, the temperature of the warehouse should be controlled in a lower environment, generally not exceeding 25 ° C.
    and should be placed in a dry place. If this compound encounters water vapor, or initiates reactions such as hydrolysis, its purity and structure will be damaged. Therefore, the humidity in the warehouse should be maintained at a relatively low level, between about 40% and 60%.
    Furthermore, it should be avoided from light. Light radiation can also promote its chemical reaction and cause changes in properties. Store in a dark place in a brown bottle or a container with a light-shielding function to reduce the impact of light on it.
    At the same time, the storage place should be well ventilated. If the environment is blocked, once this material leaks, harmful gases will accumulate, which not only endangers the safety of personnel, but may also exacerbate chemical reactions due to increased concentration.
    And it needs to be separated from oxidants, acids, bases and other substances. Because of its active chemical properties, it coexists with the above substances, or reacts violently, causing safety accidents. When storing methyl 4- (trifluoromethyl) pyridine-2-carboxylate, proper arrangements should be made in terms of temperature, humidity, light, ventilation and isolation from other substances to ensure its quality and safety.