Methyl 4 Hydroxyquinoline 2 Carboxylate
quinoline thiophene imidazole thiazole

Methyl 4-hydroxyquinoline-2-carboxylate

Taiy Chemical

    Specifications

    HS Code

    570671

    Chemical Formula C11H9NO3
    Molecular Weight 203.194 g/mol
    Appearance Solid
    Melting Point 194 - 196 °C
    Solubility In Water Low solubility
    Solubility In Organic Solvents Soluble in some organic solvents like ethanol, DMSO
    Pka Value Around 4.8 for the carboxylic acid group
    Uv Absorption Maximum Typically in the range of 250 - 350 nm
    Ir Characteristic Peaks Carbonyl peak around 1700 - 1750 cm⁻¹ (ester C=O), hydroxyl peak around 3200 - 3600 cm⁻¹ (phenolic -OH)
    Refractive Index Data may vary depending on measurement conditions
    Density Data may vary, needs experimental determination

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    Frequently Asked Questions

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    What is the chemical structure of Methyl 4-hydroxyquinoline-2-carboxylate?
    Methyl 4-hydroxyquinoline-2-carboxylate is composed of a quinoline ring, a hydroxyl group, and a carboxyl methyl ester group. The quinoline ring is a nitrogen-containing heterocyclic ring with the structure of benzopyridine. In this compound, the quinoline ring is connected with a hydroxyl group at the 4th position. This hydroxyl group has nucleophilic and active chemical properties and can participate in many reactions, such as esterification, etherification, etc. The presence of this ester group not only affects the polarity of the compound, but also plays a key role in hydrolysis, aminolysis and other reactions. The whole structure of the compound exhibits unique physical and chemical properties due to the interaction of various groups. Its structure endows the compound with potential biological activity and chemical application value, and may have important uses in pharmaceutical chemistry, organic synthesis and other fields.
    What are the main uses of Methyl 4-hydroxyquinoline-2-carboxylate?
    Methyl-4-hydroxyquinoline-2-carboxylic acid esters are widely used in the field of organic synthesis. First, they can be used as key intermediates in pharmaceutical synthesis. To cover pharmaceutical research and development, it is often necessary to construct compounds with specific structures. This ester has a unique structure and can provide a basic framework for the construction of many drug molecules. For example, some drugs with antibacterial and anti-inflammatory effects often involve this intermediate in the synthesis path. By reacting with other reagents, through clever chemical conversion, the desired drug active structure can be precisely constructed.
    Second, it also has important uses in the field of materials science. It can be modified by specific reactions and introduced into the polymer material system, giving the material unique properties. For example, it can enhance the optical properties of the material, so that the material exhibits good absorption or emission properties in specific light bands, and then is applied to the preparation of optoelectronic devices, such as organic Light Emitting Diodes.
    Furthermore, it also has potential applications in agricultural chemistry. It can be used as a lead compound, optimized and modified by structure, to develop new pesticides, such as fungicides, insecticides, etc. Due to its special chemical structure, it may be able to show efficient control effects on specific pests and diseases, and compared with traditional pesticides, it may have lower environmental toxicity and better biodegradability, which is in line with the needs of current green agriculture development.
    What are the synthetic methods of Methyl 4-hydroxyquinoline-2-carboxylate?
    The preparation of methyl 4-hydroxyquinoline-2-carboxylic acid esters has been known for a long time. Common methods include esterification of methanol with 4-hydroxyquinoline-2-carboxylic acid as the starting material and catalyzed by an acid catalyst. If sulfuric acid is used as the catalyst, under the condition of heating and reflux, the two interact to obtain methyl 4-hydroxyquinoline-2-carboxylic acid esters. In this process, the acid catalyst can increase the reaction rate and make the reaction proceed in the direction of ester formation.
    There are also those who use other compounds as the starting material and prepare them through multi-step reactions. For example, the quinoline ring system is constructed by condensation reaction of suitable aromatic amines and carbonyl compounds, and then hydroxyl and carboxyl groups are introduced, and finally esterification is carried out to obtain the target product. Although this multi-step synthesis path is complicated, it can be flexibly adjusted according to different raw materials and reaction conditions to obtain products with higher yield and purity.
    It is also prepared by metal catalysis. The selection of specific metal catalysts can make the reaction conditions milder and better selectivity. For example, some palladium-catalyzed reactions can accurately guide the reaction check point and reduce the occurrence of side reactions, so as to efficiently synthesize methyl 4-hydroxyquinoline-2-carboxylic acid esters.
    Different synthetic methods have their own advantages and disadvantages, and they need to be selected according to actual needs, such as raw material availability, cost, yield and purity requirements.
    What are the physical properties of Methyl 4-hydroxyquinoline-2-carboxylate?
    Methyl 4 - hydroxyquinoline - 2 - carboxylate is an organic compound with unique physical properties. Its properties are mostly crystalline solids, and the molecules are arranged in an orderly manner due to intermolecular forces. Stable at room temperature, because the structure contains stable groups such as aromatic rings and carboxymethyl esters.
    Looking at its appearance, it is often white to light yellow crystalline powder. The powder is fine and uniform in texture, reflecting the shape of molecular accumulation. The melting point is in a specific range, about [X] ° C - [X] ° C, and the energy required for melting is determined by the intermolecular forces. The melting point can be used for identification and purity judgment. The melting point range of pure products is narrow, and impurities will reduce the melting point and widen the range.
    In terms of solubility, it has a certain solubility in organic solvents such as ethanol and acetone. Hydrogen bonds or van der Waals forces can be formed between organic solvents such as ethanol and compound molecules to help them disperse and dissolve; the solubility in water is low, because its molecular polarity is different from water, and the molecular force between water molecules and compound molecules is weak, which is unfavorable for dissolution.
    Density is also an important physical property, about [X] g/cm ³, which is related to the molecular weight and the degree of packing. Density determines its position in the mixed system and the separation method.
    In addition, the compound has certain sublimation properties, and can be directly converted from solid state to gaseous state under specific conditions. This property may have applications in the field of separation and purification.
    The physical properties of Methyl 4 - hydroxyquinoline - 2 - carboxylate provide an important basis for its synthesis, separation, identification and application, and are of great significance to the research of chemistry and related fields.
    What is the market outlook for Methyl 4-hydroxyquinoline-2-carboxylate?
    Methyl-4-hydroxyquinoline-2-carboxylic acid ester, which has a considerable market prospect in the current market, is quite promising. Guanfu chemical industry, medicine, materials and other fields are gradually on the rise in demand for its state.
    From the perspective of medicine, the current progress of epidemic prevention and pharmaceutical research and development is rapid, and the creation of many new drugs often relies on such compounds as key intermediates. The unique chemical structure of methyl-4-hydroxyquinoline-2-carboxylic acid ester makes it unique in the display of pharmacological activity, or it can help the research and development of new drugs to make breakthroughs, so the demand for it in the pharmaceutical industry is expected to rise.
    As for the field of materials, technological evolution has promoted the increasing demand for new materials. Methyl-4-hydroxyquinoline-2-carboxylic acid esters may emerge in the synthesis of special materials due to their own characteristics, such as the preparation of optical materials and polymer materials. Therefore, with the expansion of the materials industry, its market demand will also increase.
    However, although the market prospect is good, there are also challenges. First, the production process may need to be refined in order to improve productivity and reduce costs in order to gain a favorable position in the market competition. Second, similar alternative products may also pose a threat to their market share, and they need to continue to strengthen research and development to highlight their own advantages. Overall, the methyl-4-hydroxyquinoline-2-carboxylic acid ester market has a bright future, but it also requires industry experts to study diligently and meet challenges in order to enjoy the opportunity of market development.