5 Bromo 2 Oxo 1 2 Dihydropyridine 3 Carboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid

    Specifications

    HS Code

    411042

    Name 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid
    Molecular Formula C6H4BrNO3
    Molar Mass 218.005 g/mol
    Appearance Solid (predicted)
    Melting Point No data available
    Boiling Point No data available
    Solubility In Water No data available
    Pka No data available
    Density No data available
    Flash Point No data available

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    General Information
    Where to Buy 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid in China?
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    Frequently Asked Questions

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    What is the chemical structure of 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid?
    5-Bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid, according to its name, it can be known that this is an organic compound. From its chemical nomenclature, its chemical structure can be obtained as follows:
    This compound contains a pyridine ring, which is a six-membered nitrogen-containing heterocycle and has aromatic properties. However, at 1,2-dihydropyridine, the double bond of the pyridine ring changes, and the double bond at positions 1 and 2 has only a single bond, and the second position is oxo, which means that the carbon atom at position 2 is connected to the oxygen atom by a double bond to form a carbonyl group.
    In addition, the 3-position is connected with a carboxyl group, which is a -COOH group and is acidic. The 5-position is connected with a bromine atom, and bromine, as a halogen element, is connected to the 5-position carbon atom of the pyridine ring by a single bond.
    Its overall structure can be briefly described as follows (only schematic, not precise structural formula): In the pyridine ring, the 1 and 2 positions are connected by a single bond, the 2-position is connected to a carbonyl group, the 3-position is connected to a carboxyl group, and the 5-position is connected to a bromine atom. This chemical structure endows the compound with unique chemical properties. The presence of carbonyl groups allows it to participate in reactions such as nucleophilic addition, the acidity of carboxyl groups can cause it to neutralize with bases, and bromine atoms can participate in substitution reactions. It may have important uses in the field of organic synthesis.
    What are the common synthesis methods of 5-bromo-2-oxo-1, 2-dihydropyridine-3-carboxylic acid?
    The common synthesis methods of 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid are similar to the processes recorded in "Tiangong Kaiwu", and need to be explored from different paths.
    First, pyridine derivatives are used as starting materials. By carefully selecting suitable pyridine compounds, under specific conditions, they are brominated. This process requires precise control of the reaction temperature, time and proportion of reactants. For example, a pyridine derivative is selected, and the brominating reagent is slowly added dropwise in a specific organic solvent. When the reaction number is stirred at the appropriate temperature, the bromine atom accurately replaces the hydrogen atom at the target position to complete the bromination step. Then, a specific position on the pyridine ring is oxidized to generate the desired carbonyl group, that is, the 2-oxo structure. This step requires selecting a suitable oxidizer, controlling the reaction conditions, and making the oxidation reaction proceed smoothly and accurately. Finally, 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid is obtained.
    Second, a cyclization reaction strategy is adopted. A chain compound containing a suitable functional group is used as the starting material. Under the action of a specific catalyst, cyclization reactions can occur between these functional groups. For example, select a carbon chain with appropriate spacing, with reactive functional groups at both ends, and in the presence of a catalyst, heat or in a specific solvent environment to promote the formation of intramolecular rings. During the reaction, close attention should be paid to the reaction conditions to prevent side reactions from occurring. After the ring is formed, a specific position on the ring is modified, bromine atoms and carboxyl groups are introduced, and the final product is synthesized through gradual reactions.
    Third, with the help of multi-step reaction combination. First, the basic framework of the pyridine ring is constructed by using common organic reactions, and then bromine atoms, oxo groups and carboxyl groups are gradually introduced into the ring. Each step of the reaction requires the selection of suitable reagents and conditions according to the reaction mechanism. For example, the pyridine ring is first constructed, then brominated at a suitable position, then oxidized to form a 2-oxo structure, and finally a carboxyl group is introduced. The whole process requires fine planning of the reaction sequence to ensure the smooth connection of each step, so as to efficiently synthesize 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid.
    What are the main physical properties of 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid
    5-Bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid, this is an organic compound. Its main physical properties are quite important, and it is related to its performance in various chemical processes and practical applications.
    Looking at its properties, under normal temperature and pressure, it is mostly in the form of a solid state, usually a powder or crystalline substance, which is easy to store and operate.
    When it comes to melting point, due to the interaction of specific chemical bonds and functional groups in the molecular structure, its melting point is within a certain range, but the exact value will vary according to the synthesis method and purity. This melting point characteristic is a key reference index in the separation, purification and identification of compounds.
    Solubility is also one of the key properties. The solubility of this compound in organic solvents varies from polar organic solvents such as methanol and ethanol, or it exhibits a certain solubility, because some functional groups in the molecule can form intermolecular forces with polar solvent molecules, such as hydrogen bonds; while in non-polar solvents, such as n-hexane, the solubility is poor, because the molecule has a certain polarity, and the force between it and the non-polar solvent is weak.
    Furthermore, its stability cannot be ignored. In view of the presence of bromine atoms, carbonyl groups and pyridine rings in the molecular structure, under certain conditions, chemical reactions may occur, which affects its stability. For example, in the environment of light, high temperature or the presence of specific chemical reagents, the substitution reaction of bromine atoms may be triggered, or the addition and oxidation reactions involving carbonyl groups may be initiated.
    In addition, the density of the compound is also one of its physical properties. Although the exact density data is also affected by factors such as purity, the density is of great significance in the consideration of the relationship between the mass and volume of the substance and the study of mixed systems.
    In summary, the physical properties of 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acids, such as their properties, melting point, solubility, stability, and density, play an indispensable role in understanding the chemical behavior and practical applications of this compound.
    Where is 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid used?
    5-Bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid, which is useful in the fields of medicine, pesticides and materials.
    In the field of medicine, it is a key intermediate for the synthesis of a variety of specific drugs. Due to its unique chemical structure, it can participate in the construction of molecules with specific pharmacological activities. For example, in the development of some antihypertensive drugs, this compound plays an important role. Its structure helps to precisely regulate the interaction between the drug and the biological target, so that the drug can act more effectively on the relevant physiological mechanisms, so as to achieve the purpose of lowering blood pressure. Furthermore, in the development of anti-tumor drugs, 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acids also show potential. After appropriate modification and transformation, it may generate active substances that can interfere with tumor cell proliferation and induce tumor cell apoptosis, providing a new way to conquer cancer.
    In the field of pesticides, new pesticides can be created from this raw material. Its chemical properties can give pesticides unique insecticidal, bactericidal or herbicidal properties. For example, synthetic new insecticides, by virtue of the specific combination of the compound structure with specific enzymes or receptors in pests, disrupt the normal physiological metabolism of pests, and then effectively kill pests. And compared with traditional pesticides, such new pesticides based on 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acids may have higher selectivity and lower environmental toxicity, which is more suitable for the current green agricultural development needs.
    It can also be seen in the field of materials. In the synthesis of functional materials, it can be introduced into polymer materials as a structural unit. In this way, special properties such as light response and thermal stability can be given to materials. For example, a new type of photochromic material prepared, 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid, undergoes specific changes in structure under light stimulation, causing the material to change color, which has great application prospects in anti-counterfeiting, optical sensors, etc. Or, it can be used to improve the thermal stability of polymer materials, so that they can still maintain good physical properties in high temperature environments, and broaden the application range of materials.
    What is the market prospect of 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid?
    5-Bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid, this product is in the market and has good prospects.
    In today's chemical industry, pharmaceutical synthesis has been booming. This compound is very important in the pharmaceutical industry. Its unique structure is often a key raw material when creating new drugs. Many scientific research teams and pharmaceutical companies are focusing on the research and development of new drugs based on it.
    In the production of innovative drugs, more focus on anti-cancer, anti-inflammatory and other fields. Due to its chemical properties, it can interact with specific targets in organisms and is expected to lead to new drugs with excellent efficacy. Therefore, the demand for 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid is expected to rise steadily.
    Furthermore, with the advance of science and technology, the chemical synthesis process is also constantly innovating. New methods for synthesizing this acid may be more efficient, environmentally friendly, and cost-effective. If the cost is reduced, its application scope can be expanded, and it may emerge in other fields such as materials science, except medicine.
    However, its market also faces challenges. Regulations and regulations are becoming increasingly stringent, and the development cycle of new drugs is long and expensive. To launch new drugs made from this acid to the market requires many tests. However, despite the difficulties, in view of its potential value, 5-bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid still has a broad market potential in the future, with promising prospects, which will attract continued attention and investment from the industry.