6 Dimethoxymethyl 1 2 Dihydro 2 Oxo 3 Pyridinecarboxylic Acid
pyridine pyrrole pyrazine piperidine piperazine

6-(dimethoxymethyl)-1,2-dihydro-2-oxo-3-pyridinecarboxylic acid

    Specifications

    HS Code

    366644

    Chemical Formula C9H11NO6
    Molecular Weight 229.19
    Appearance Solid (likely white or off - white powder)
    Solubility In Water Limited solubility (due to polar - non - polar balance)
    Solubility In Organic Solvents Soluble in some polar organic solvents like ethanol
    Acidity Weakly acidic due to carboxylic acid group
    Reactivity Can react with bases, alcohols (esterification)
    Stability Stable under normal conditions but may decompose under heat or strong acidic/basic conditions

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    General Information
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    Frequently Asked Questions

    As a leading 6-(dimethoxymethyl)-1,2-dihydro-2-oxo-3-pyridinecarboxylic 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 is the chemical structure of 6- (dimethoxymethyl) -1,2 - dihydro - 2 - oxo - 3 - pyridinecarboxylic acid
    The chemical structure of 6- (dimethoxymethyl) -1,2-dihydro-2-oxo-3-pyridinecarboxylic acid is described as follows:
    The main structure of this compound is a pyridine ring. The pyridine ring is a nitrogen-containing six-membered heterocyclic ring, which is connected by five carbon atoms and one nitrogen atom in a specific order. At position 2 of the pyridine ring, there is a carbonyl group (C = O). The carbon atom in this carbonyl group is connected to the oxygen atom by a double bond, giving this position a specific chemical activity and reaction tendency. At position 6, there is a dimethoxy methyl group, which is connected by a central carbon atom with two methoxy groups (-OCH) and a hydrogen atom. The oxygen atom in the two methoxy groups is connected to the central carbon atom by a single bond, and the central carbon atom is connected to the No. 6 carbon atom of the pyridine ring by a single bond. At position 3, there is a carboxyl group (-COOH), which is composed of a carbonyl group (C = O) and a hydroxyl group (-OH), and is connected to the No. 3 carbon of the pyridine ring by a single bond through the carbon atom in the carbonyl group. This chemical structure determines that the compound has unique physical and chemical properties, and has potential applications in many fields such as organic synthesis and medicinal chemistry.
    What are the main uses of 6- (dimethoxymethyl) -1,2 - dihydro - 2 - oxo - 3 - pyridinecarboxylic acid
    6- (dimethoxymethyl) -1,2-dihydro-2-oxo-3-pyridine carboxylic acid has a wide range of uses. In the field of medicine, it can be used as a key intermediate to help synthesize many drugs with unique therapeutic effects. For example, when developing drugs to treat specific inflammatory diseases, this compound can participate in key reaction steps. With its special chemical structure, it can be cleverly combined with other substances to generate molecules with precise anti-inflammatory activity, providing the possibility for patients to relieve pain.
    In the field of materials science, it is also useful. Due to its structural properties, it can be modified by specific reactions and then used to prepare functional polymer materials. For example, through a reasonable polymerization reaction, it can be introduced into the polymer chain, endowing the material with special solubility, stability or optical properties, etc., which plays an important role in the creation process of new materials.
    Furthermore, in the field of organic synthetic chemistry, the compound acts as an important synthetic building block, providing a foundation for the construction of complex organic molecules. Chemists can expand the molecular structure according to its structural characteristics and use various organic reactions, such as nucleophilic substitution and condensation reactions, to create organic compounds with novel structures and specific functions, which greatly enriches the variety of organic compounds and lays the foundation for subsequent research and application. In conclusion, 6 - (dimethoxy methyl) - 1,2 - dihydro - 2 - oxo - 3 - pyridine carboxylic acids have shown important value and broad application prospects in many fields.
    What is the synthesis method of 6- (dimethoxymethyl) -1,2 - dihydro - 2 - oxo - 3 - pyridinecarboxylic acid
    The synthesis of 6- (dimethoxymethyl) -1,2-dihydro-2-oxo-3-pyridine carboxylic acid is an important topic in the field of organic synthesis. This compound has great application potential in the fields of medicine and pesticides, so its synthesis method has attracted much attention.
    To synthesize this compound, it can be achieved through a multi-step reaction. The choice of starting materials is crucial, and pyridine derivatives with suitable substituents are often selected. In the first step, the pyridine ring may be modified to introduce specific substituents. If a pyridine derivative is used as the starting material, under suitable reaction conditions, the nucleophilic substitution reaction is used to react the halogenated alkane with a specific position on the pyridine ring, and the methoxy group is introduced. This step requires careful selection of the reaction solvent and base to ensure the smooth progress of the reaction.
    The second step may require the construction of a dihydro-2-oxo structure. Carbonyl groups can be introduced on one side of the pyridine ring through oxidation reaction. This process requires the selection of a suitable oxidizing agent, such as a mild oxidizing agent, to avoid excessive oxidation and ensure the selectivity of the product. And the reaction temperature, time and other conditions need to be strictly controlled to optimize the reaction yield.
    Furthermore, for the introduction of carboxyl groups, a specific reaction path can be used. For example, a certain intermediate containing ester groups can be hydrolyzed under alkaline conditions and then acidified to obtain the carboxyl group of the target compound. This hydrolysis reaction requires attention to the concentration of the base and the reaction time to prevent it from affecting other groups.
    Synthesis of 6- (dimethoxymethyl) -1,2-dihydro-2-oxo-3-pyridine carboxylic acid requires fine design of the reaction route, strict control of the reaction conditions of each step, and precise separation and purification of the intermediate in order to obtain it efficiently.
    What are the physicochemical properties of 6- (dimethoxymethyl) -1,2 - dihydro - 2 - oxo - 3 - pyridinecarboxylic acid
    6 - (dimethoxy methyl) - 1,2 - dihydro - 2 - oxo - 3 - pyridine carboxylic acid, this is an organic compound. Its physical and chemical properties are unique, let me tell you in detail.
    Look at its properties, under normal temperature and pressure, or as a solid state. This compound has a specific melting point, which is the temperature at which the substance changes from solid to liquid state. Its melting point is crucial for the identification and purification of this compound. When the temperature rises to the melting point, the substance begins to melt into a liquid state.
    In terms of solubility, it is in common organic solvents, or exhibits some solubility. Organic solvents, such as ethanol, acetone, dichloromethane, etc. In ethanol, or can be moderately dissolved, because the polarity of ethanol interacts with the partial structure of the compound, so that the molecule can be dispersed in the solvent. However, in water, its solubility or poor, because the hydrophobic part of the structure accounts for a large proportion, the interaction with water is weak.
    The chemical properties of this compound are also quite critical. In its molecular structure, the pyridine ring is aromatic, giving it a certain chemical stability. However, the carboxyl group attached to the ring is acidic. The carboxyl group can undergo acid-base neutralization reaction under appropriate conditions, such as when encountering a base, to generate the corresponding carboxylate. The methoxy group of the dimethoxy methyl part can undergo substitution reaction under the action of specific reagents, so as to modify the structure of the compound and expand its application in the field of organic synthesis. The physicochemical properties of this compound lay an important foundation for its application in chemical synthesis, drug development, and many other fields.
    What is the price range of 6- (dimethoxymethyl) -1,2 - dihydro - 2 - oxo - 3 - pyridinecarboxylic acid in the market?
    I haven't heard the exact price range of "6- (dimethoxymethyl) -1,2-dihydro-2-oxo-3-pyridinecarboxylic acid" on the market. The price of this compound may vary widely due to its use, purity, and supply and demand.
    If it is used in pharmaceutical research and development, it will be expensive due to strict requirements on purity and complicated preparation process. For general chemical research, the purity requirements are slightly lower, and the price may be relatively affordable.
    And in different places, the price varies due to different transportation costs and local market supply and demand. In the prosperous city of Dayi, there are many chemical reagent suppliers, with fierce competition, and the price may be flat; in remote places, the supply is inconvenient, and the price may be high.
    And different suppliers have different pricing strategies. Well-known big manufacturers are good at quality and after-sales, and the price may be high; emerging manufacturers, to expand the market, or take a low price strategy.
    In summary, to know the exact price range of this compound, when consulting chemical reagent suppliers, compare the quotations of different merchants, you can get it.