5 Bromo 2 Trifluoromethyl Pyridine 4 Carboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

5-BROMO-2-(TRIFLUOROMETHYL)PYRIDINE-4-CARBOXYLIC ACID

    Specifications

    HS Code

    408136

    Chemical Formula C7H3BrF3NO2
    Molar Mass 270.003 g/mol
    Appearance Solid (presumably, based on common nature of such compounds)
    Solubility In Water Limited (due to hydrophobic fluorine and bromine groups)
    Solubility In Organic Solvents Soluble in polar organic solvents like DMSO, DMF (common for such heterocyclic carboxylic acids)

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    As a leading 5-BROMO-2-(TRIFLUOROMETHYL)PYRIDINE-4-CARBOXYLIC ACID 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 5-bromo-2- (trifluoromethyl) pyridine-4-carboxylic acid?
    5-Hydroxy-2- (trifluoromethyl) pyridine-4-carboxylic acid is an organic compound. This substance has the following physical properties:
    Appearance properties are often white to light yellow crystalline powder. This appearance feature makes it easy to distinguish from other substances in appearance, which is of great significance for substance identification and preliminary judgment.
    Melting point is in a specific range, usually around 140-145 ° C. As an important physical constant of a substance, melting point is of great significance for its purity identification and state prediction under specific conditions. By measuring the melting point, the purity of the substance can be determined. If the measured melting point is consistent with the standard value, it indicates that the purity is high; if it deviates, it may contain impurities. In terms of solubility, it is slightly soluble in water, but soluble in common organic solvents, such as dichloromethane, N, N-dimethylformamide, etc. This solubility characteristic plays a key role in the process of organic synthesis, separation and purification. In the organic synthesis reaction, choosing a suitable organic solvent as the reaction medium can fully dissolve the substance and participate in the reaction; when separating and purifying, according to its solubility difference, use extraction and other means to achieve separation from impurities.
    In terms of stability, it is relatively stable under normal storage and use conditions. However, it should be noted that it has certain requirements for humidity and temperature. If the humidity is too high or the temperature is too high, it may cause degradation or other chemical reactions, which will affect the quality and performance. Therefore, it should be stored in a dry and cool place to ensure its stability.
    What are the chemical properties of 5-bromo-2- (trifluoromethyl) pyridine-4-carboxylic acids?
    5-Hydroxy-2- (trifluoromethyl) pyridine-4-carboxylic acid, this is an organic compound. Its chemical properties are quite diverse, let me talk about them one by one.
    First of all, its acidity is acidic because it contains carboxyl groups, so it is acidic and can be neutralized with bases. For example, if it meets sodium hydroxide, the hydrogen of the carboxyl group can be combined with hydroxide ions to form water and the corresponding carboxylate. This is a common acid-base reaction, just like extinguishing fire with water, and the two interact to achieve a new equilibrium.
    Let's talk about its nucleophilic substitution reaction characteristics. The substituents on the pyridine ring can affect the reaction activity. The specific position of the pyridine ring of the compound is vulnerable to attack by nucleophiles due to the distribution of electron clouds. Nucleophiles are like warriors, attacking the relatively low density of the electron cloud, which in turn triggers nucleophilic substitution reactions and generates new compounds. It is like a "war" in the microscopic world. The old structure is broken and a new order is established.
    In the field of organic synthesis, 5-hydroxyl-2- (trifluoromethyl) pyridine-4-carboxylic acid can be used as a key intermediate. Due to its unique structure, it can be connected with other organic molecules through a series of chemical reactions to build more complex organic compounds. It is like building a building block, using it as the basic module, constantly combining to create "buildings" of different shapes. In the field of medicinal chemistry, using this as the starting material, through multi-step reactions, or drug molecules with specific pharmacological activities can be synthesized, which contributes to human health.
    In addition, its stability can also be described. The existence of trifluoromethyl in the molecule, due to its strong electron absorption, changes the overall electronic structure of the molecule, which affects the stability of the compound to a certain extent. The group acts as a strong barrier, making some parts of the molecular structure more stable and resisting external factors from damaging its structure. However, this may also affect its activity in participating in certain reactions, which is a matter of mutual advantage and disadvantage. It needs to be weighed in practical applications.
    What are the main uses of 5-bromo-2- (trifluoromethyl) pyridine-4-carboxylic acid?
    5-Hydroxy-2- (triethyl) pyridine-4-carboxylic acid, which has important uses in many fields.
    In the field of medicinal chemistry, it is a key intermediate in drug synthesis. Through clever chemical reactions, it can be integrated into the molecular structure of drugs. For example, when developing specific antibacterial drugs, 5-hydroxy-2- (triethyl) pyridine-4-carboxylic acid can precisely combine with other active groups by virtue of its unique chemical structure, thereby endowing the drug with more excellent antibacterial activity and pharmacological properties. Through structural modification and modification, the therapeutic effect of drugs can be optimized and side effects can be reduced, providing a solid foundation and rich possibilities for the creation of new antibacterial drugs.
    In the field of materials science, it can be used to prepare functional materials with special properties. For example, in the process of designing new optoelectronic materials, the compound can be used as a core structural unit, and its electronic properties and spatial configuration can exert a significant impact on the optical and electrical properties of the material. When introduced into the polymer material system, it can effectively regulate the key parameters such as the fluorescence emission wavelength, luminous efficiency and charge transport capacity of the material, thus preparing high-performance materials with broad application prospects in display technology, optoelectronic devices and other fields.
    In the field of organic synthesis chemistry, 5-hydroxy- 2- (triethylmethyl) pyridine-4-carboxylic acid is an extremely important starting material and reaction intermediate. Because its molecular structure contains multiple active reaction check points, it can participate in a variety of organic chemical reactions, such as esterification reaction, amidation reaction, cyclization reaction, etc. Through carefully designed reaction routes, a series of complex and novel organic compounds can be constructed on the basis of them, which provides a rich material basis and innovative ideas for the development of organic synthesis chemistry, and effectively promotes the continuous progress of organic synthesis methodology.
    What are the synthesis methods of 5-bromo-2- (trifluoromethyl) pyridine-4-carboxylic acid?
    To prepare 5-bromo-2- (trifluoromethyl) pyridine-4-carboxylic acid, the method is as follows:
    First, the compound containing the corresponding pyridine structure can be started. First, the pyridine ring is brominated with a suitable halogenating agent, such as bromine or N-bromosuccinimide (NBS), under suitable reaction conditions. This reaction requires the selection of appropriate solvents, such as dichloromethane, carbon tetrachloride, etc., and in a certain temperature range, or room temperature, or heated reflux, depending on the activity of the substrate. After bromination, trifluoromethyl is introduced. The nucleophilic substitution reaction can be carried out with trifluoromethylation reagents, such as trifluoromethyl magnesium halide, trifluoromethyl lithium, etc., in an anhydrous and oxygen-free environment at low temperature. Finally, the specific position on the pyridine ring is carboxylated. The Grignard reagent can be used to react with carbon dioxide. The Grignard reagent at the corresponding position on the pyridine ring is first prepared, and then carbon dioxide gas is introduced. After acidification treatment, the target 5-bromo-2 - (trifluoromethyl) pyridine-4-carboxylic acid can be obtained.
    Second, it can also think in reverse and gradually construct the pyridine ring from simple raw materials. First, suitable halogenated hydrocarbons, bromine-containing atoms and groups that can be converted into trifluoromethyl groups, and nitrogen-containing compounds, such as nitriles, amides, etc., are condensed in organic solvents under basic conditions to construct the prototype of the pyridine ring. This process requires strict control of the reaction conditions, such as the type and dosage of bases, the reaction temperature and time. Then the pyridine ring is modified to introduce carboxyl groups through suitable reactions. The Grignard reagent method mentioned above can be used, or other methods such as hydrolysis of carboxyl-containing precursors, such as ester hydrolysis, etc., and finally 5-bromo-2- (trifluoromethyl) pyridine-4-carboxylic acid can be obtained.
    Third, the reaction path catalyzed by transition metals can also be used. The coupling reaction is carried out in a basic environment with the action of the aryl halide containing bromine and trifluoromethyl and the precursor containing the pyridine ring, assisted by the ligand under the action of the transition metal catalyst, such as palladium catalyst and nickel catalyst. This reaction requires high selection of catalysts and ligands, and needs to be carefully screened according to the substrate structure and reactivity. After the reaction, the specific position is converted into carboxyl group after subsequent functional group conversion, and the synthesis of 5-bromo-2- (trifluoromethyl) pyridine-4-carboxylic acid is achieved.
    What is the market price of 5-bromo-2- (trifluoromethyl) pyridine-4-carboxylic acid?
    The price of potassium pyridine-4-carboxylate, 5-% -2- (Sanxiangmethyl), has been studied in detail in today's market. This product has its effect in all kinds of usage, so its price also changes from time to time and varies from market to market.
    I have heard that the price of Ja people is determined by many ends. First, the price of raw materials is also. If the price of all raw materials relied on by 5-% -2- (Sanxiangmethyl) potassium pyridine-4-carboxylate rises, the price of the finished product will also rise. For example, if the production of raw materials is difficult to obtain due to changes in time and geographical conditions, the price will be high, and the price of this product will not be equal.
    Second, the simplicity and effort of the system. If making this thing requires exquisite skills and lengthy processes, and the labor is cumbersome and the money is countless, then the price is expensive. On the contrary, if the system is easy and simple, and the cost is small, the price may be slightly flat.
    Furthermore, the supply and demand of the city. If the world uses this thing, and the demand exceeds the supply, the price will rise; if the supply exceeds the demand, fills the market, and no one cares, the price will be suppressed.
    There are various external reasons, such as government regulations and taxation systems, all of which are related to the price. If the government decree is strict, and there are many regulations to control this thing, Jia people will have to pay a lot, and the price will also be higher because of it; the tax will increase, and the cost of Jia people will not only increase, but will also be changed to the price, so that the price will be higher than in the past.
    Looking at the recent situation, the price of 5-% -2- (Sanxiangmethyl) potassium pyridine-4-carboxylate is about [X] money to [X] money per catty. However, this is only the price of one place at a time, and it cannot be generalized. In the northern and southern regions, there is a difference in supply and demand, and the price may vary by a few dollars. And times change, and the price of other days cannot be determined according to today's number. The changing market conditions are unpredictable, and Jia people need to judge the situation in order to profit from the trade move, and those who know the price can also benefit from it.