3 Quinolinecarboxylic Acid 6 Bromo 4 Chloro Ethyl Ester
quinoline thiophene imidazole thiazole

3-quinolinecarboxylic acid, 6-bromo-4-chloro-, ethyl ester

Taiy Chemical

    Specifications

    HS Code

    671673

    Name 6 - bromo - 4 - chloro - 3 - quinolinecarboxylic acid ethyl ester
    Chemical Formula C12H9BrClNO2
    Molar Mass 314.56 g/mol
    Appearance Solid (usually, appearance can vary based on purity and preparation)
    Melting Point Data may vary depending on purity, needs experimental determination
    Boiling Point Data may vary depending on purity, needs experimental determination
    Solubility In Water Low solubility, quinoline esters are generally hydrophobic
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform, etc.
    Density Data may vary depending on purity, needs experimental determination
    Pka Data may vary, related to the acidic nature of the carboxylic acid part in certain environments

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    Frequently Asked Questions

    As a leading 3-quinolinecarboxylic acid, 6-bromo-4-chloro-, ethyl ester 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 ethyl 6-bromo-4-chloro-3-quinoline carboxylate?
    6-Hydroxy-4-alkane-3-tetraphosphoester ethyl acetate, this is a rather special chemical substance. Its physical properties are rich and diverse, let me tell them one by one.
    Looking at its appearance, it is often a colorless to slightly yellow transparent liquid, with a pure texture. Under the light, its transparent texture can be seen, just like a clear spring, flowing with a soft luster.
    When it comes to smell, it exudes an elegant and unique fragrance, not a pungent smell, but like a light floral fragrance in the spring breeze, which is haunting. Although it is not rich, it has a unique charm and is soothing to the body and mind.
    As for the boiling point, it is about a specific temperature range. When the external environment reaches this temperature range, the substance will gradually change from liquid to gaseous state, like a feather flying, following the law of material transformation. This boiling point characteristic is of critical significance in many links such as chemical production and purification, and is related to the accuracy and efficiency of operation.
    In terms of melting point, it is also within a certain value range. At this temperature, the substance quietly changes from solid to liquid state, just like a sleeping thing waking up and starting a different form journey. This melting point value provides an important basis for storing and transporting the substance. If the temperature is not properly controlled, or its shape changes, it will affect the quality.
    Solubility is also an important physical property. In organic solvents, such as common ethanol, ether, etc., it exhibits good solubility and can be fused with it to form a uniform and stable mixed system, just like water emulsion blending, regardless of each other. In water, the solubility is relatively limited, only a little can be dissolved, showing a state of partial fusion, which determines its application scope in different environments.
    In terms of density, compared with water, it has a specific density value. When mixed with water, it can be stratified according to density differences, or floating on water or sinking underwater. This property plays an important role in separation, identification and other operations.
    The physical properties of 6-hydroxy- 4-alkane-3-square photoester-based ethyl acetate each have their own unique features and are related to each other, which together constitute a comprehensive picture of their characteristics and lay the foundation for their applications in chemical, pharmaceutical and other fields.
    What are the chemical synthesis methods of ethyl 6-bromo-4-chloro-3-quinoline carboxylate?
    To prepare ethyl 6-bromo-4-fluoro-3-methoxybenzoate, there are various methods.
    First, it can be started from the corresponding benzoic acid derivative. First, a suitable halogenating agent, such as a brominating agent, is used to brominate a specific position of the benzene ring under specific reaction conditions to introduce bromine atoms. Next, a suitable fluorinating agent is selected, and the fluorine atom is introduced into the target position through a series of reaction steps. Then, a methoxy group is added through an etherification reaction with a methoxy group-containing agent. Finally, the obtained benzoic acid product is esterified with ethanol under acid catalysis or other suitable conditions to obtain ethyl 6-bromo-4-fluoro-3-methoxybenzoate.
    Second, we can start from another class of aromatic compounds. First, the benzene ring structure containing the desired substituent is constructed through clever reaction strategies. For example, some benzene derivatives with potentially convertible groups are used as raw materials, and bromine, fluorine and methoxy are introduced in sequence by rearrangement and substitution reactions. When the substituents on the benzene ring are properly arranged, the esterification reaction is carried out, and the target product is synthesized in a suitable reaction system with ethanol as the esterification reagent.
    Third, or you can try to use halogenated aromatics as starting materials. Through metal-catalyzed coupling reactions, such as palladium-catalyzed reactions, they are coupled with bromine, fluorine, and methoxy-containing reagents in sequence to gradually build the required substituent structure. After the benzene ring is partially constructed, esterification is carried out to achieve the synthesis of 6-bromo-4-fluoro-3-methoxybenzoate ethyl ester. These various methods have their own advantages and disadvantages, and they need to be carefully considered according to the actual situation, such as the availability of raw materials, the difficulty of reaction, yield and purity requirements, etc., and choose the best one.
    In which fields is ethyl 6-bromo-4-chloro-3-quinoline carboxylate used?
    6-Bromo-4-fluoro-3-pyridinecarboxylate ethyl ester has a wide range of uses. In the field of pharmaceutical research and development, it is a key intermediate in organic synthesis. It can be cleverly combined with other compounds through specific chemical reactions to create new drugs with unique pharmacological activities. For example, in the synthesis process of some antibacterial and antiviral drugs, it can act as an important starting material. After multi-step reactions, it can build the core structural framework of drugs and help to develop innovative drugs with better efficacy and fewer side effects.
    In the field of materials science, it can also play an important role. Due to its unique chemical structure, it can be used to prepare functional materials with special properties. For example, in the synthesis of organic photoelectric materials, the introduction of this substance can effectively adjust the electron cloud distribution and energy level structure of the material, thereby improving the photoelectric conversion efficiency of the material, providing strong support for the development of solar cells, organic Light Emitting Diodes and other fields.
    In the field of fine chemicals, 6-bromo-4-fluoro-3-pyridinecarboxylate ethyl ester is also indispensable. It can be used as an important raw material for the synthesis of fine chemicals such as special fragrances and additives. Through a carefully designed synthesis route, it can be converted into fine chemical products with unique aromas or specific functions, meeting the needs of different industries for high-quality fine chemicals.
    In summary, ethyl 6-bromo-4-fluoro-3-pyridinecarboxylate has shown important application value in many key fields such as medicine, materials and fine chemicals due to its unique chemical properties, and has made significant contributions to technological innovation and product upgrading in various fields.
    What is the market price of ethyl 6-bromo-4-chloro-3-quinoline carboxylate?
    Today there is 6-hydroxy- 4-alkane-3-square photophospheric ethyl acrylate, what is the price of its market? This question is also related to business affairs. However, the price is often different due to changes in time, place, quality and supply and demand, and cannot be determined.
    In the city of husband, where the situation changes, the price is determined, not only the quality of the product. The place of production is different, but the cost of transportation is different. If the product is near the city, the freight will be saved, and the price will be cheap; if it is far away from the ocean, the cost will be huge, and the price will also increase.
    It is different from time to time, and the price is also different. When the demand for this product is high, everyone competes to buy it, and although the price is high, the price will rise; if it needs to be low, the goods will accumulate in the market, and they will not be able to sell it, and the price will be reduced to promotion.
    Good quality is also the key to price. Those who are of high quality are loved by everyone, and they are willing to pay a high price to buy it; those who are of poor quality, even if the price is low, few people will care about it.
    As for the way of supply and demand, if the supply exceeds the demand, the price will fall; if the supply exceeds the demand, the price will rise. If there are many producers of this product, the market is full of goods, and the demand is scarce, the price will tend to decline; on the contrary, if there are few producers, there are many seekers, and the price will < Br >
    Therefore, in order to know the market price of 6-hydroxy- 4-alkane-3-cubic photophospheric ethyl acrylate, it is necessary to carefully consider the situation of time, place, quality and supply and demand.
    What are the safety and toxicity of ethyl 6-bromo-4-chloro-3-quinoline carboxylate?
    6-Hydroxy-4-fluoro-3-benzyloxybenzoate ethyl ester, this substance is related to safety and toxicity, and is discussed in detail.
    Its chemical structure is considered, and functional groups such as 6-hydroxy, 4-fluoro, and 3-benzyloxybenzoate are integrated. This kind of structure is unique in both chemical reactivity and biological activity. Its safety consideration is first in stability. From the perspective of molecular composition, each atom interacts with functional groups to form a certain spatial structure and electron cloud distribution. Although its performance under various extreme conditions is not known in detail, under normal circumstances, if there is no external strong incentive, such as high temperature, high pressure, strong acid and alkali, or specific catalysts, the molecular structure should be relatively stable, and few spontaneous violent decomposition or other dangerous reactions occur.
    As for toxicity, it can be discussed from two aspects. First, from the perspective of biological activity, the functional groups of the compound may interact with various biomacromolecules in organisms, such as proteins and nucleic acids. Fluorine atoms may affect the affinity and specificity of molecular binding to biological targets due to their high electronegativity. If this compound enters the organism, 6-hydroxyl groups may participate in the formation of hydrogen bonds, change protein conformation or affect the active center of enzymes, thereby interfering with normal physiological and biochemical processes. The benzyloxy part, because of its large spatial resistance and hydrophobicity, may affect the permeability and distribution of molecules in biofilms. Second, from a metabolic point of view, when an organism metabolizes a foreign compound, it will try to convert it into a form that is easier to excrete from the body. During the metabolism of this compound in vivo, it may produce intermediate products, and the toxicity of these intermediate products cannot be ignored.
    However, in order to determine its safety and toxicity, rigorous experimental verification is required. Cytotoxicity can be preliminarily assessed through in vitro cell experiments, such as the use of a variety of cell lines, to observe changes in cell morphology, proliferation, apoptosis and other indicators. It is also necessary to conduct animal experiments to investigate its toxic effects at the overall animal level, including acute toxicity, subacute toxicity, chronic toxicity, etc., to explore its effects on different tissues and organs. In this way, the safety and toxicity of 6-hydroxy- 4-fluoro-3-benzyloxybenzoate can be accurately understood.