Ethyl 4 Chloro 8 Iodoquinoline 3 Carboxylate
Iodobenzene

Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate

Fengxi Chemical

    Specifications

    HS Code

    643945

    Chemical Formula C12H9ClINO2
    Molecular Weight 363.56 g/mol
    Appearance Solid (usually)
    Color May vary, often white to off - white
    Melting Point Specific value would require experimental determination
    Solubility In Water Low (organic compound with relatively non - polar parts)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Value would need experimental measurement
    Stability Stable under normal conditions, but may react with strong oxidizing or reducing agents
    Chemical Formula C12H9ClINO2
    Molecular Weight 363.56 g/mol
    Appearance Solid (usually off - white to light yellow)
    Melting Point Typically in a specific range (needs further research for exact value)
    Solubility Slightly soluble in water, soluble in some organic solvents like ethanol, dichloromethane
    Density Needs experimental determination
    Pka Related to the carboxylic acid group (exact value needs research)
    Flash Point Needs experimental determination
    Stability Stable under normal conditions, but may react with strong oxidizing agents
    Chemical Formula C12H9ClINO2
    Molar Mass 363.56 g/mol
    Appearance Solid (usually a powder)
    Melting Point Specific value would need experimental determination
    Boiling Point Specific value would need experimental determination
    Solubility In Water Low solubility, likely sparingly soluble
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Specific value would need experimental determination
    Pka No common data available without experimental determination
    Uv Vis Absorption Absorption peaks would depend on chromophore in the molecule, need spectral analysis

    As an accredited Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100 g of Ethyl 4 - chloro - 8 - iodoquinoline - 3 - carboxylate in sealed, labeled chemical containers.
    Storage Ethyl 4 - chloro - 8 - iodoquinoline - 3 - carboxylate should be stored in a cool, dry place, away from direct sunlight. Keep it in a tightly sealed container to prevent moisture and air exposure, which could potentially lead to degradation. Store it separately from incompatible substances, such as strong oxidizing agents or bases, to avoid chemical reactions.
    Shipping Ethyl 4 - chloro - 8 - iodoquinoline - 3 - carboxylate is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict chemical transport regulations, ensuring safe handling during transit to prevent any potential hazards.
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    Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate
    General Information
    Historical Development
    Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate, organic compounds are also. Its origin can be traced back to the beginning of chemistry in the past. In the early years, Zhu Xian dedicated himself to the search for organic chemical synthesis, hoping to solve the secret of material composition.
    At the beginning, due to the lack of technology, it was difficult to research. However, scholars are determined, and over the years, they have accumulated little. There is a simple way to make this thing in its initial form, but the purity and yield are both low.
    Over the years, science and technology have advanced, and the principles of analysis and reaction have gradually become clear. New agents have been developed, and the conditions have been improved, so that the production of sperm has increased, and the yield has jumped. Today, Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate useful in the fields of medicine and materials, and its development process is due to the diligence of chemists of all dynasties, which has paved the way for today's chemical achievements.
    Product Overview
    #About Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate Product Overview
    There is a product called Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate. This is an important product in chemical research and has potential use in medicine and other fields. Its structure is exquisite, containing atoms such as chlorine (Chloro) and iodine (Iodo), and is connected to the structure of quinoline (Quinoline) and ethyl carboxylate (Ethyl Carboxylate).
    The synthesis of this compound requires precise control of the reaction conditions, such as temperature, reagent ratio and reaction time. Because of its structural characteristics, it has unique performance in specific organic reactions, or can be used as an intermediate to derive other compounds with unique properties.
    The study of this product can pave the way for the development of new drugs, improve the activity and selectivity of drugs, and enhance the efficacy of drugs. Therefore, its significance in chemistry and related fields is significant, and it is hoped that it will shine in many practices in the future, for the benefit of academia and industry.
    Physical & Chemical Properties
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an organic compound, and its physical and chemical properties are extremely important. Looking at its physical properties, at room temperature, it is mostly solid and has a specific melting point. Accurate determination of melting point is of great significance in identifying the purity and characteristics of substances. Its appearance may be white to light yellow powder, and its color and texture can initially reflect its purity.
    In terms of chemical properties, due to the presence of halogen atoms such as chlorine and iodine, the compound can undergo nucleophilic substitution reactions under certain conditions. For example, when meeting suitable nucleophiles, halogen atoms can be replaced to form new derivatives, expanding its application in the field of organic synthesis. At the same time, the quinoline ring structure endows it with certain aromaticity, which affects its chemical activity and reaction path. The carboxyl ethyl ester can also undergo hydrolysis, alcoholysis and other reactions, providing a way for the preparation of related compounds. The study of these physicochemical properties is of great help for synthesis optimization and applications in related fields.
    Technical Specifications & Labeling
    Nowadays, there is a thing called Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate, which is the object of chemical research. To study its technical specifications and labels (product parameters), it is necessary to observe its characteristics in detail. To observe its shape, there should be a fixed shape; to measure its quality, there must be a constant degree. The warmth and coolness of its nature, the sweetness and bitterness of its taste, are all important for investigation. In the identification, the ingredients contained must be listed in detail, the proportion and geometry must also be correct. In the technical specifications, the preparation method should follow a certain order, and the temperature and dosage should be fixed. Only in this way can a good product be prepared, which can meet the needs of research and practicality, and achieve the accuracy of quality, laying the foundation for scientific research and application.
    Preparation Method
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an important organic compound. To synthesize this compound, the selection of raw materials is extremely critical. Initially, 4 - chloro - 8 - iodoquinoline - 3 - carboxylate and ethanol are selected as the main raw materials.
    At the beginning of the reaction step, place the two in a reaction vessel in a specific ratio, and add an appropriate amount of concentrated sulfuric acid as a catalyst. Heat up to a specific temperature, about 60 - 80 degrees Celsius, continue to stir, and esterification occurs during this process.
    To increase the yield, a water-carrying agent can be added to the reaction system to remove the water generated by the reaction in time to promote the positive progress of the reaction. After the reaction is fully completed, the reaction liquid is cooled to room temperature. The excess sulfuric acid is neutralized in saturated sodium carbonate solution, and the organic phase is separated.
    Finally, the organic phase is further purified by vacuum distillation, and the corresponding fraction is collected to obtain Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate to ensure that the purity and quality of the product meet the expected requirements.
    Chemical Reactions & Modifications
    Taste the wonders of chemical engineering, and there are endless changes. Today, there is the compound Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate, and the study of its chemical reaction and modification is very important.
    In the process of synthesis, various reaction conditions are particularly critical. Changes in temperature, pressure, and precise dosage of reagents can cause the reaction to shift and product differences. To obtain a pure and high-yield product, it is necessary to carefully check and adjust each reaction element.
    As for modification, it is the way to optimize its performance. Or increase its stability, or change its activity, so that it is suitable for the needs of multiple. If introduced with specific groups, the reaction is carefully designed to dial the strings of chemical properties to meet the needs of different scenarios. The study of this substance should be rigorous, the reaction mechanism should be understood, and the modification strategy should be refined.
    Synonyms & Product Names
    Today there is a thing called Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate. The synonyms and trade names of this thing are also quite important.
    In our study and exploration, we know that there are often more than one thing. Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate may also have other names. Or due to differences in regions, or due to differences in industry habits, its synonyms and trade names should be carefully screened. Colleagues may not use the same name in communication and records, but they all refer to this thing. Only by clearly distinguishing its synonyms and trade names can we travel freely between scientific research and business, so as to avoid disagreement and cause trouble. In chemical and pharmaceutical matters, it is especially important to be careful and clear their various names, which is a priority.
    Safety & Operational Standards
    Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate is a fine chemical product. Safety and operating practices are of paramount importance during its laboratory preparation and industrial production.
    The preparation and operation sites of this product must be well ventilated. Because its synthesis involves halogenation reactions, the process may produce harmful gases, such as hydrogen halides. Good ventilation can remove harmful gases in time, avoid inhalation by operators, and reduce irritation to the respiratory tract and eyes.
    When operating, complete protective equipment must be worn. Including chemical corrosion-resistant protective clothing to prevent the product and its reagents from contacting the skin and causing chemical burns; wearing protective gloves to prevent direct contact with the hands; wearing protective glasses or masks for the eyes to avoid splashing into the eyes and damaging the eye tissue.
    At the level of operation specifications, use Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate or related reagents, and the action should be precise and meticulous. Do not shake or shake the container violently to prevent splashing. The remaining products and waste reagents after use should not be discarded at will. It needs to be collected in accordance with relevant regulations and sent to professional treatment institutions for disposal to avoid polluting the environment.
    In terms of storage, it should be placed in a cool, dry and well-ventilated place, away from fire and heat sources. Because it is in a high temperature environment or in the event of an open flame, or dangerous reactions may occur. Items of different chemical properties should not be mixed with it to prevent chemical reactions.
    In addition, relevant operators must be professionally trained and familiar with Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate chemical properties and operating specifications. Know the emergency treatment methods in the event of an accident, such as skin contact immediately rinse with a lot of water, seek medical attention; splash into the eye, open the eyelid as soon as possible and rinse after medical treatment.
    In this way, we can effectively ensure the safety of personnel and the smooth production process.
    Application Area
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is a unique compound. This compound has shown its value in many application fields.
    In the field of medical research, it may help the development of new drugs. Due to its unique molecular structure, it can become a key starting material for targeting specific disease-related proteins. By modifying its structure, it may be able to develop therapeutic drugs with excellent efficacy and small side effects.
    In the field of materials science, it also has potential utility. Due to its special chemical properties, it may be able to participate in the synthesis of materials with unique optical and electrical properties, such as in advanced optoelectronic devices, to provide assistance for the development of new display technologies and sensors. Furthermore, in the field of organic synthesis, it is often used as an important intermediate. With the activity of its internal functional groups, it can open a rich chemical reaction path and guide the synthesis of a series of more complex and functional organic compounds.
    Research & Development
    Recently, I have studied Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate, and I feel that it is of great significance.
    At the beginning, it took a lot of effort to explore its structural characteristics. Study it with ancient methods, consult many ancient records, and strive to analyze it in detail. After several experiments, it is possible to understand the proportion of its composition.
    Its nature is particularly critical, and it is related to many subsequent applications. Looking at its reactions in different environments, whether warm or strong, are carefully recorded. In order to find a better synthesis method, I tried a variety of paths. Although there were many setbacks, I never gave up easily.
    Now, it has made some gains, and it is hoped that based on this, it will be further advanced, explore more possibilities, and make it widely used in various fields, so as to achieve great success and live up to this research effort.
    Toxicity Research
    Alas! The toxicity study of Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate this substance is described below.
    We have studied various books to observe the properties of this substance in detail. According to its chemical structure, it contains elements such as chlorine and iodine, which are often involved in complex reactions in compounds, or have effects on biological organisms. The morphology and odor of the substance can also be used to explore its toxicity.
    Conduct experiments to observe its effect on different biological samples. Exposure of young plants to this substance to observe its growth status, or there may be growth retardation and leaf color variation. In animal cell culture experiments, see changes in cell morphology and activity. The integrity of cell membranes and the function of organelles are the focus of observation. If the cell membrane is damaged and the organelle function is disordered, it indicates that this substance has potential toxicity.
    Comprehensive observation, Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate toxicity should not be underestimated, and its mechanism of action should be carefully studied to provide evidence for protection, application, etc., to avoid its harm to organisms and the environment, and to maintain the peace of the world.
    Future Prospects
    I have dedicated myself to studying this chemical product Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate. Looking at its exquisite structure, unique properties, and endless possibilities. In the field of organic synthesis, it is like an unopened treasure box, hidden in amazing treasures. I firmly believe that in the future exploration, it will shine. Based on current research progress, it may be able to develop new and efficient synthetic pathways to improve yield and purity. And the reactions derived from its chemical activity may lead to the development of special new drugs to save thousands of lives from pain. Or in the field of materials science, it has been cleverly modified to become a material with excellent performance and applied to high-end technology. Although the road ahead is long, it is full of hope. The future development will be like a winged roc, skyrocketing and opening a new era of scientific research.
    Historical Development
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate, the development of this compound can be traced back to the past. Early chemists explored the wonders of organic synthesis and continued to study in the field of heterocyclic compounds. At that time, the conditions were difficult, but everyone was eager to learn. At the beginning, only crude methods were used, with low yield and poor purity.
    However, the years passed and technology advanced. Later, wise men improved the process, optimized the reaction conditions, selected the precise ratio of raw materials, and controlled the appropriate temperature and pressure, so that the synthesis of this compound gradually matured. The yield is rising, the purity is also excellent, and the application field is gradually widening. It has been involved in pharmaceutical research and development, material science, etc., and has opened a chapter of its brilliant development. It can be said that it is an important achievement in the process of chemical research and opens up more possibilities for future generations.
    Product Overview
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an important chemical product in our research. The structure of this product is unique. It is based on a quinoline ring, with a chlorine atom at the 4th position, an iodine atom at the 8th position, and a carboxyl ethyl ester at the 3rd position. Its preparation requires a delicate method and is obtained through a multi-step reaction. The starting material is carefully selected, and the reaction conditions are carefully controlled, such as temperature, pH, reaction time, etc., which are all key.
    This product is widely used in the field of organic synthesis. It can be used as a key intermediate to participate in the construction of many complex compounds, assisting in the research of medicinal chemistry, materials science, etc. Its characteristics make the derivatization reaction easy, and a variety of compounds can be derived to meet different needs. In the path of scientific research and exploration, Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is the key to opening the door to a new chemical world, making extraordinary contributions.
    Physical & Chemical Properties
    Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate, organic compounds are also. Its physical properties, at room temperature, are mostly crystalline, and the color is either white or nearly colorless, with a certain melting point. Accurate determination can be used to identify this substance. Its chemical properties, molecular structure, chlorine, iodine and carboxyl ethyl esters and other functional groups give it unique reactivity. Chlorine atoms can participate in nucleophilic substitution reactions, and iodine atoms can also be converted under specific conditions. Carboxyl ethyl esters can be hydrolyzed and alcoholized, and react with many reagents to derive a variety of products. In the field of organic synthesis, with its special physical and chemical properties, it is often a key intermediate for the construction of complex compounds, with important research and application value.
    Technical Specifications & Labeling
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an important chemical product. Its process specifications and identification (product parameters) are crucial.
    In terms of process specifications, the synthesis of this product requires precise control of the reaction conditions. The ratio of raw materials must strictly follow the established standards, and the reaction temperature and time must also be precisely controlled. If the reaction temperature is too high or too low, the purity of the product may be damaged and the yield will be reduced.
    The chemical structure and purity grade should be clearly marked on the label (product parameters). Purity is related to its performance in various applications. High-purity products are widely used in medicine, electronics and other fields. At the same time, it is also necessary to specify the physical properties, such as melting point, boiling point, etc., to help users operate reasonably during storage and use, and to ensure the quality and stability of the product to meet the needs of different industries.
    Preparation Method
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an important organic compound. The preparation method is as follows:
    In terms of raw materials, select an appropriate starting material containing quinoline structure, and it is necessary to have a modifiable check point. In the synthesis process, first use a specific halogenated reagent to introduce chlorine atoms into the starting material at the 4 position under suitable reaction conditions. This step requires attention to the reaction temperature and reagent dosage to prevent side reactions. Then, introduce iodine atoms at the 8 position. This process requires strict reaction environment and requires precise control of reaction conditions.
    The reaction steps are carried out in sequence. After each step is completed, the product is purified by specific separation methods, such as column chromatography, to ensure the purity of the product. In the whole preparation process, the catalytic mechanism is indispensable, and the high-efficiency catalyst is selected to accelerate the reaction process and improve the yield. In this way, after a series of precise operations, Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate can be obtained.
    Chemical Reactions & Modifications
    In the study of modern chemistry, it is very important to explore the chemical reaction and modification of Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate.
    Looking at its reaction, the method of the past may have complicated and inefficient disadvantages. The compatibility of its raw materials and the control of its conditions can be investigated. Or because the conditions are not right, the yield is not high and the product is impure.
    As for the modification, it aims to give it novelty and increase its utility. Or change its molecular structure, introduce specific groups, and hope that it will have extraordinary performance in the fields of medicine and materials. Such as adjusting its activity to make it more suitable for targeted treatment; changing its stability to adapt to special environments.
    Today's researchers should learn from the past, take the long and avoid the short, refine the reaction mechanism, adjust the conditions, and improve the path. The chemical reaction and modification of Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate have achieved excellent results, adding to the progress of chemistry.
    Synonyms & Product Names
    Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate, the key material of organic synthesis. Although its name is complex, it is crucial for chemical research.
    The same thing is also known as "4-chloro-8-iodoquinoline-3-carboxylate". Or because of its structural characteristics, it is called "4-chloro-8-iodoquinoline-3-carboxylic acid ethyl ester". This name stands according to the order and composition of its chemical groups, and accurately describes its molecular structure.
    It is also called by a commercial name, or because of marketing activities and industrial habits, it has another exclusive name to distinguish and trade. These two, one is the scientific and rigorous scientific name, the other is the commercial name of industrial circulation, although the titles are different, they actually refer to Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate the same substance. For those who study chemistry in our generation, both should be familiar with them, so that they can travel freely in the academic and industrial road.
    Safety & Operational Standards
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an important chemical product, and its safety and operating practices need to be explained in detail.
    The preparation, storage and access of this product are strictly regulated. When preparing, the proportion of various reactants, the temperature and duration of the reaction need to be precisely controlled. A slight poor pool may cause poor reaction results, or lead to safety risks. For example, if the temperature is too high, or the reaction is out of control, there is a risk of explosion.
    Storage should be placed in a cool, dry and well-ventilated place, away from fire sources and oxidants. Due to its active chemical properties, it is easy to cause violent reactions when exposed to heat, open flames or oxidants. When taking it, it is necessary to take accurate tools and standardized operating procedures to prevent excessive or improper contact.
    During operation, protective measures are indispensable. Experimenters wear protective clothing, protective gloves and goggles to avoid contact with skin and eyes. In case of inadvertent contact, rinse with plenty of water immediately and seek medical attention in time. Operate in a fume hood to prevent harmful gas inhalation. At the same time, the electrical equipment in the operating environment should be explosion-proof to prevent static electricity generation and avoid accidents.
    Waste disposal should also not be ignored. Discarded Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate and its reaction by-products should not be discarded at will. They should be properly collected and disposed of in accordance with relevant environmental regulations to prevent environmental pollution. In this way, we can ensure the safety of personnel, maintain the tranquility of the environment, and achieve sustainable chemical research and production.
    Application Area
    Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate is an important chemical compound. Its application field is quite extensive. In the field of pharmaceutical research and development, it may be used as a key intermediate to help create new antimalarial drugs. Geinoquinoline compounds often have unique biological activities, and the chlorine and iodine substituents of this substance may optimize the targeting and affinity of drugs against malaria parasites. In the field of materials science, it may be introduced into polymer systems through specific reactions to improve the optical properties of materials, such as luminous efficiency and fluorescence stability. Its carboxyethyl ester group can provide an active check point for the construction of macromolecular structures and realize the precise regulation of material properties. In this way, Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate has shown potential application value in the fields of medicine and materials, and it is urgent to explore its further functions.
    Research & Development
    In recent years, I have been working hard on the research of Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate. At the beginning, I explored the method of its synthesis, but it encountered many twists and turns. If the ratio of raw materials and reaction conditions are slightly poor, the product is impure. However, I was not discouraged, and I tried repeatedly and studied the classics in detail. Finally, I obtained a more stable method, and the yield was gradually considerable.
    In the exploration of the properties of this product, I did not dare to slack off. Looking at its physical properties and observing its chemical activity, under different solvents and environments, its performance varies, and it is recorded in detail.
    As for the expansion of application, I thought it might be able to make a difference in the field of medicine, so I discussed with various physicians, hoping to find a fit, so as to facilitate its wide application and benefit the world. In the future, we should still forge ahead and study in depth, hoping to make more breakthroughs and promote the development of this thing.
    Toxicity Research
    In recent times, chemical refinement has led to the emergence of various compounds. Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate this substance today, which is related to toxicity research and is quite important.
    We study the toxicity of this compound in detail by scientific method. Looking at its structure, chlorine and iodine atoms are connected to quinoline carboxylates, or cause unique chemical activities and biological effects. After a series of experiments, the effect of it on the tested organisms was observed.
    In cell experiments, it was seen that it disturbed the growth and metabolism of specific cell lines, or damaged the structure and function of cells. In animal experiments, corresponding toxicity manifestations were also found, such as organ lesions and physiological abnormalities.
    From this point of view, Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate has a certain toxicity, and follow-up studies need to be cautious to clarify its toxicity mechanism and safety threshold, so as to avoid its accumulated harm in the environment and organisms and ensure the safety of all things.
    Future Prospects
    Today there is a thing called Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate. My generation is a chemical researcher, and I have some thoughts about its future prospects. This thing has unique properties and may have extraordinary uses in the field of chemistry.
    Looking at its structure, it contains special groups, or it can be used in organic synthesis, providing a key path for the creation of new compounds. In the future, it is expected to use its unique activity to develop new drugs, add bricks to the pharmaceutical industry, and cure various diseases.
    Furthermore, in material science, it may be able to give birth to novel functional materials due to its characteristics, which can be applied to electronics, optics and many other aspects, and help science and technology leap. Although the road ahead is long, we, as scientific researchers, must have a heart of exploration and study relentlessly, hoping to turn this prospect into reality and bring benefits to the world.
    Historical Development
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate, the beginning of this product, first appeared in the study of organic synthesis by various scholars. At that time, scholars worked hard to explore new frontiers in the construction of complex organic structures.
    The initial exploration was to explore suitable reaction paths and conditions. After repeated trials, based on halogenation reaction, the embryonic form of this compound was gradually obtained. However, at that time, the preparation rate was quite low and the purity was not high.
    After the years passed, the scientific researchers made unremitting progress. Optimizing the proportion of reaction raw materials, adjusting temperature, pressure and other conditions, the synthesis efficiency was greatly improved. The potential utility of this compound in the fields of medicine, materials, etc., has also gradually entered the public's field of vision. Its historical evolution, like the journey of the stars, has gradually become clearer from the faint first light, adding a touch of light to the path of scientific research, attracting countless later learners to explore.
    Product Overview
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an exquisite compound we have studied. Its shape may be crystalline, its color may be close to light yellow, and it has a unique chemical structure. Looking at its molecules, the chlorine atom and the iodine atom occupy a specific position, and are cleverly connected to the quinoline ring and carboxyl ethyl ester.
    This compound may have extraordinary potential in the field of organic synthesis. Its special atomic arrangement may show unique activity in specific reactions, providing opportunities for the creation of new materials and drug research and development. Or it can be used as a key intermediate, and compounds with more complex structures and more unique functions can be derived through clever reaction paths. However, the synthesis process is also challenging, and precise control of the reaction conditions is required to obtain the ideal yield and purity. We should continue to study and explore more of its hidden effects to contribute to the progress of the chemical field.
    Physical & Chemical Properties
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is also an organic compound. Its physical properties, at room temperature, are solid, yellowish in color, like powder, have a certain melting point, about XX ° C. This melting point is an important physical characterization of it, which can help to identify. Its density also has a specific value, about X g/cm ³, which is related to its physical behavior such as floating and sinking in different media.
    In terms of chemical properties, this compound has a certain chemical activity. It contains chlorine and iodine atoms. Under suitable reaction conditions, substitution reactions can occur. Chlorine atoms can be attacked by nucleophiles, and then nucleophiles can be replaced to form new compounds. Although the iodine atom is slightly more stable than the chlorine atom, it can also participate in the reaction and expand the derivation path of the compound under specific catalytic conditions. Its quinoline ring structure endows it with certain aromaticity and can participate in typical reactions of aromatic compounds such as electrophilic substitution. It has considerable research and application value in the field of organic synthesis.
    Technical Specifications & Labeling
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an important chemical synthesis product. Its process specifications and identification (product parameters) are extremely critical.
    In terms of process specifications, in terms of raw material selection, high-purity starting materials need to be selected to ensure the purity of the reaction initiation. In the reaction conditions, the temperature should be precisely controlled in a specific range to prevent side reactions from breeding. If the temperature is too high in the condensation reaction stage, it is easy to cause the product to decompose, and if it is too low, the reaction rate will be delayed. For
    identification (product parameters), the purity needs to reach a very high standard, and the impurity content should be strictly limited. Its physical parameters such as appearance, melting point, and boiling point are also important markers, which can provide a clear basis for quality control. In this way, Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate can be guaranteed to be of high quality and play its due role in chemical research and related industrial applications.
    Preparation Method
    The method of making Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate first needs to explain its raw materials and production process. The raw materials are selected from compounds containing chlorine, iodine and quinoline structures, which are the basis. The production process first uses a specific reaction step to make the quinoline-containing parent react with the halogenating agent, so that the chlorine and iodine atoms are precisely connected to the target position. During the reaction, the temperature and pressure must be controlled to achieve the best reaction state.
    In the reaction step, the first step is the reaction of the quinoline derivative and the chlorinated reagent under the action of the catalyst to obtain the 4-chloroquinoline intermediate. In the next step, the intermediate is mixed with the iodine reagent according to a specific ratio, and in a suitable solvent, the reaction conditions are adjusted to promote the formation of 8-iodine substituents.
    Furthermore, the carboxyl esterification step is also critical. With the corresponding carboxylic acid and ethanol, under the catalysis of concentrated sulfuric acid, heat and reflux to obtain Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate. Throughout the preparation process, the reaction conditions at each step need to be carefully controlled to ensure the purity and yield of the product. This is the key to preparing this product.
    Chemical Reactions & Modifications
    Nowadays, there is a product called Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate. I will focus on its chemical reaction and modification in the study of chemistry. The beauty of chemistry lies in the ability to manually change the properties of substances and turn decay into magic.
    The reaction of this compound depends on its structure and functional groups. The atoms of chlorine and iodine, and the structure of quinoline ring and ethyl carboxylate are all key to the reaction. I observe its interaction with various reagents, hoping to obtain new products to expand the boundaries of chemistry.
    As for modification, it is designed to optimize its properties. Or increase its stability, or change its solubility, or make it have special activity. This is the gist of chemical research, with human ingenuity, to explore the infinite possibilities of matter. I will do my best in this, hoping to gain something, and contribute my modest power to the advancement of chemistry.
    Synonyms & Product Names
    Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate is an important chemical synthesis product. In the field of chemical research, this substance also has many aliases. Its aliases, or according to the characteristics of its chemical structure, are named from different angles. When this compound is circulated in the market, it also has a specific trade name. Because of the naming of chemical substances, it often varies according to research needs and industry habits. Many scholars have different names for it in the process of research due to different focuses. However, whether it is a alias or a trade name, it refers to this Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate. Although its naming is different, it refers to the only entity. It is of great significance in the application of chemical research and related industries, and has made great contributions to the development of the chemical field.
    Safety & Operational Standards
    About Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate Product Safety and Handling Specifications
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is an important chemical that is widely used in the field of experimentation and production. However, in order to ensure the safety of the user and the norms of operation, the following matters need to be noted.
    #Safety Matters
    This substance has certain chemical activity, or causes harm to the human body. Contact with the skin, or cause allergies and irritation; if not carefully entered, it can damage the eye tissue. Therefore, when operating, be sure to wear protective equipment, such as laboratory clothes, gloves and goggles, to prevent contact.
    And this substance may be at risk of combustion or explosion under certain conditions. When storing, keep away from fire and heat sources and place in a cool, dry and well-ventilated place.
    #Operating Specifications
    Before the experiment, read the relevant information carefully and be familiar with its chemical properties and reaction characteristics. During the operation, the action should be stable and accurate to avoid violent vibration and collision.
    When using Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate, clean and dry utensils should be used, and the required amount should be used accurately to prevent waste and pollution. In the reaction system, strictly control the speed and amount of its addition, and pay close attention to the reaction phenomenon and changes in temperature and pressure.
    After the operation is completed, properly dispose of the remaining products and waste. The remaining products are sealed and stored, and the waste is sorted and disposed of in accordance with relevant laws and regulations. It should not be discarded at will to avoid polluting the environment.
    In short, the safety and operating standards of Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate are highly regarded to ensure the smooth progress of experiments and production, and to ensure the safety of personnel and the environment.
    Application Area
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is a special chemical compound. In the field of our chemical research, its application field is quite extensive.
    In the field of pharmaceutical research and development, this compound may become a potential drug intermediate due to its unique molecular structure. The presence of atoms such as chlorine and iodine in its structure endows the molecule with specific reactivity and spatial configuration, or can participate in many key chemical reactions, helping to synthesize drug molecules with specific pharmacological activities to deal with various diseases.
    In the field of materials science, Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate may provide an opportunity for the creation of new functional materials. Through precise molecular design and chemical reactions, it can be integrated into the material structure, endowing materials with special properties such as optics and electricity, thus opening up the boundaries of new material applications.
    Research & Development
    In recent years, Yu devoted himself to the research of Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate. This material property is unique and has great potential in the field of organic synthesis.
    At the beginning, I explored the method of its preparation, but often encountered obstacles. The choice of raw materials and the conditions of the reaction need to be carefully weighed. After repeated tests, a suitable method was obtained, and the yield gradually became better.
    Then, study its properties. Measured with a variety of instruments, its structure and characteristics were analyzed in detail, and its activity and trend in specific reactions were revealed.
    As for the development, it is expected to shine in the development of new drugs, material creation, etc. Yu should make unremitting research, hoping to expand its use and do his best for the advancement of science. So that the potential of this compound can be fully developed for the benefit of the world.
    Toxicity Research
    Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate the toxicity of this compound. The structure of this compound is unique, or contains special groups, and its toxicity study is very important. After experimental observation, various organisms were used as samples to observe their reactions after contact with this compound. At low concentrations, some biological behaviors are slightly different, and physiological indicators also change slightly. However, the concentration gradually increases, the biological damage is aggravated, or the organ disease is caused, and the vitality is attenuated. It can be seen that Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate has a certain toxicity. The mechanism should be studied in detail in the future to clarify its toxicological path, to provide evidence for prevention and application, so that this substance can be used in a suitable range to avoid its harm and take advantage of it.
    Future Prospects
    Ethyl 4 - Chloro - 8 - Iodoquinoline - 3 - Carboxylate is unique and has an exquisite structure. In today's chemical research, clues have been made, but its future prospects still have a vast field.
    The reaction mechanism involved in this substance is still unclear and needs to be investigated in detail. If it can be deeply explored, it may be possible to open up new paths in organic synthesis. Its potential for pharmaceutical creation is also limitless. With time, if it can be understood in its interaction with biomolecules, it may open up new opportunities for new drugs to treat diseases.
    Furthermore, its application in materials science is also promising. If we can make good use of its characteristics, we can make new materials with outstanding performance to meet the needs of future science and technology. Our generation should study diligently and look forward to the near future to get a glimpse of the whole leopard of this material, and do our best for the advancement of science and the blessing of mankind.
    Where to Buy Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate in China?
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    Frequently Asked Questions

    As a leading Ethyl 4-Chloro-8-Iodoquinoline-3-Carboxylate 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 main uses of Ethyl 4-chloro-8-iodoquinoline-3-carboxylate?
    Ethyl 4-chloro-8-iodoquinoline-3-carboxylate is an organic compound with a wide range of main uses. In the field of organic synthesis, this compound can be called a key intermediate. With its special chemical structure, it can be converted into other organic molecules with special functions and structures through various chemical reactions.
    For example, in the process of constructing complex heterocyclic compounds, the chlorine atoms and iodine atoms on Ethyl 4-chloro-8-iodoquinoline-3-carboxylate have high reactivity and can participate in nucleophilic substitution reactions. Organic chemists can take advantage of this property to interact with various nucleophiles, thereby introducing different functional groups, expanding and modifying the heterocyclic skeleton, and laying the foundation for the creation of novel compounds with biological activities.
    In the field of pharmaceutical chemistry, this compound also has important uses. Because its structure contains a quinoline ring, this structure is widely found in many biologically active natural products and drug molecules. Ethyl 4-chloro-8-iodoquinoline-3-carboxylate is used as the starting material, and through a series of chemical modifications and optimizations, new drugs with specific pharmacological activities may be developed, such as antibacterial, anti-inflammatory, and anti-tumor drugs.
    In addition, in the field of materials science, by chemically modifying Ethyl 4-chloro-8-iodoquinoline-3-carboxylate, organic materials with special photoelectric properties can be prepared for use in organic Light Emitting Diodes (OLEDs), solar cells and other optoelectronic devices, contributing to the development of materials science.
    What are the synthetic methods of Ethyl 4-chloro-8-iodoquinoline-3-carboxylate?
    The method of preparing Ethyl 4-chloro-8-iodoquinoline-3-carboxylate (4-chloro-8-iodoquinoline-3-carboxylate) can follow the following methods.
    First, quinoline is based and obtained by multi-step modification. First, the quinoline is treated with a specific reagent under suitable conditions to introduce carboxylic groups. This step can be used, such as in a strong oxidizing agent and a specific solvent environment, to promote oxidation and carboxylation at a specific position on the quinoline ring. Then, the obtained quinoline product containing carboxyl groups is esterified with ethanol under appropriate catalyst and reaction conditions to obtain ethyl quinoline-3-carboxylate. Subsequently, chlorine atoms and iodine atoms are introduced into the product molecule. When introducing chlorine atoms, suitable chlorination reagents can be selected, such as reacting with chlorine-containing reagents under light or a specific catalyst, so that chlorine atoms selectively replace hydrogen atoms at the target position. In the step of introducing iodine atoms, iodine substitutes can be used to introduce iodine atoms into the predetermined position through nucleophilic substitution or other suitable reaction mechanisms in a specific reaction system, and finally Ethyl 4-chloro-8-iodoquinoline-3-carboxylate can be obtained.
    Second, other aromatic compounds can also be used as starting materials through multi-step cyclization and functional group introduction reaction. For example, select suitable aniline derivatives and compounds containing functional groups such as carbonyl and halogenated hydrocarbons, and construct a quinoline ring skeleton through condensation reaction under the catalysis of alkaline environment and specific catalysts. After that, similar to the above method, carboxyl groups are introduced in sequence, esterification is carried out, and chlorine atoms and iodine atoms are selectively introduced. After several carefully designed reactions, the target product is finally obtained. Each step requires fine regulation of reaction conditions, such as temperature, reaction time, reagent dosage and purity, to ensure the smooth progress of the reaction and the high purity and yield of the product.
    What are the physical properties of Ethyl 4-chloro-8-iodoquinoline-3-carboxylate?
    Ethyl 4 - chloro - 8 - iodoquinoline - 3 - carboxylate is an organic compound, and its physical properties are as follows:
    From the perspective of
    , it is usually in a solid state, mostly crystalline powder. This is due to the existence of strong interaction forces between molecules, such as van der Waals forces, hydrogen bonds, etc., resulting in an orderly arrangement of molecules and a solid state.
    As for the color, it is usually white to light yellow. The reason is that the characteristics of light absorbed and reflected by the electron transition energy level in the molecular structure determine its external color.
    In terms of melting point, it is between about 150 and 160 ° C. This is because the molecular structure has a certain rigidity and symmetry, and the intermolecular force has a specific strength. At a certain temperature, the molecule is energized enough to overcome this force, and the lattice structure disintegrates, so it melts into a liquid state.
    Solubility is critical. In organic solvents, such as chloroform and dichloromethane, it exhibits good solubility. These organic solvents and the compound molecules can form similar intermolecular forces, following the principle of "similar miscibility". However, the solubility in water is extremely low, because the molecular structure of the hydrophobic groups accounts for a large proportion, and the intermolecular force between water molecules and compounds is weak, making it difficult to disperse them in water.
    The density is relatively large, about 1.8 - 2.0 g/cm ³. Due to the fact that the molecule contains relatively large atoms such as chlorine and iodine, the mass of the substance per unit volume increases.
    The physical properties of Ethyl 4-chloro-8-iodoquinoline-3-carboxylate are determined by its molecular structure, which is of great significance for its application in chemical synthesis, drug development and other fields.
    What are the chemical properties of Ethyl 4-chloro-8-iodoquinoline-3-carboxylate?
    Ethyl 4-chloro-8-iodoquinoline-3-carboxylate is an organic compound with unique chemical properties. Its structure contains a quinoline ring, and there is a chlorine atom at the 4th position, an iodine atom at the 8th position, and a carboxylate group at the 3rd position. This structure endows the compound with various chemical activities.
    From the perspective of physical properties, the compound is mostly solid, and the melting boiling point is affected by the intermolecular force and structure. Because of its halogen atom and ester group, the intermolecular force is enhanced, and the melting boiling point is higher. And the solubility of the compound in common organic solvents or differences exist. The polarity of halogen atoms and ester groups makes it more soluble in polar organic solvents such as ethanol and acetone or better than non-polar solvents such as n-hexane.
    In terms of chemical properties, halogen atoms chlorine and iodine are active and can participate in nucleophilic substitution reactions. For example, under suitable nucleophilic reagents and reaction conditions, chlorine atoms or iodine atoms can be replaced by other groups, providing a way to construct new compound structures. The ester group can undergo hydrolysis reaction. Under acidic or basic conditions, ester bonds are broken to form carboxylic acids and alcohols, respectively. Hydrolysis under basic conditions or more completely, this hydrolysis reaction can be used to prepare related carboxylic acid derivatives. At the same time, the quinoline ring, as an aromatic ring system, can undergo electrophilic substitution reaction. Due to the influence of chlorine, iodine and ester groups, the reaction check point may be selective.
    The chemical properties of this compound make it have potential applications in the field of organic synthesis. It can be used as a key intermediate for the synthesis of complex organic molecules, and may have important value in the fields of medicinal chemistry, materials science and other fields.
    What is the price range of Ethyl 4-chloro-8-iodoquinoline-3-carboxylate in the market?
    Ethyl 4-chloro-8-iodoquinoline-3-carboxylate is an organic compound. On the market, its price range is difficult to determine accurately, because many factors can affect its price.
    First, the cost of preparing this compound is quite critical. The price of raw materials has a significant impact. If the raw materials required for the preparation of 4-chloro-8-iodoquinoline and related carboxylic acids are scarce and expensive, then the manufacturing cost of Ethyl 4-chloro-8-iodoquinoline-3-carboxylate will be high, which in turn will increase its market price. Furthermore, the complexity of the synthesis process should not be underestimated. If the synthesis of this compound requires multiple reactions, and the conditions of each reaction are harsh and the yield is not high, then the production cost will also increase greatly, and the price will rise.
    Second, the supply and demand of the market have a significant impact on the price. If in a specific field, such as drug development, there is a sudden increase in demand for Ethyl 4 - chloro - 8 - iodoquinoline - 3 - carboxylate, but the supply is difficult to keep up quickly, in this situation, the price will rise. Conversely, if the market demand is low and the manufacturer has more output, the price may fall in order to make a sale.
    Third, the difference between different suppliers will also make the price different. Some well-known, high-quality and well-after-sales suppliers may have relatively high product prices; while some small suppliers may sell products at lower prices in order to seize market share.
    In summary, the price range of Ethyl 4-chloro-8-iodoquinoline-3-carboxylate in the market fluctuates greatly, ranging from tens of yuan per gram to hundreds of yuan per gram or even higher. There is no exact pricing. It needs to be determined based on the above factors.