Methyl 3 Iodopyridine 4 Carboxylate
Iodobenzene

Methyl 3-Iodopyridine-4-Carboxylate

Fengxi Chemical

    Specifications

    HS Code

    424685

    Chemical Formula C7H6INO2
    Molecular Weight 263.03
    Appearance Solid (usually white to off - white)
    Melting Point Typically in a certain range, e.g., around 140 - 145°C (approximate value)
    Solubility In Water Poorly soluble
    Solubility In Organic Solvents Soluble in some common organic solvents like dichloromethane, chloroform
    Density [X] g/cm³ (approximate value)
    Chemical Formula C7H6INO2
    Molecular Weight 263.03 g/mol
    Appearance Solid (usually white to off - white powder)
    Melting Point Data may vary, typically in a certain temperature range
    Solubility Soluble in some organic solvents like dichloromethane, less soluble in water
    Purity Can be available in various purity levels, e.g., 95%, 98% etc.
    Density Data may be available in literature for specific conditions
    Stability Should be stored under appropriate conditions to avoid decomposition
    Chemical Formula C7H6INO2
    Molar Mass 263.03 g/mol
    Appearance Solid (presumed, as typical for many organic esters)
    Melting Point Data may vary, specific value needs further literature search
    Boiling Point Data may vary, specific value needs further literature search
    Solubility In Water Low solubility (organic ester with polar and non - polar parts)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Pka No specific data provided, but the pyridine nitrogen can be basic
    Density Data may vary, specific value needs further literature search
    Flash Point Data may vary, specific value needs further literature search

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

    Packing & Storage
    Packing 100g of Methyl 3 - iodopyridine - 4 - carboxylate in a sealed, chemical - resistant bottle.
    Storage Methyl 3 - iodopyridine - 4 - carboxylate should be stored in a cool, dry place, away from heat sources and direct sunlight. It is best kept in a tightly sealed container to prevent exposure to air and moisture, which could potentially lead to degradation. Store it separately from incompatible substances to avoid chemical reactions. Keep it in a well - ventilated area, and ensure the storage location is clearly labeled for easy identification and safety.
    Shipping Methyl 3 - iodopyridine - 4 - carboxylate is shipped in well - sealed, corrosion - resistant containers. Shipment follows strict chemical transport regulations, ensuring proper handling to prevent damage and environmental or safety risks during transit.
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    Methyl 3-Iodopyridine-4-Carboxylate
    General Information
    Historical Development
    Methyl 3-Iodopyridine-4-Carboxylate is also a product of organic chemistry. Back to its origin, the academic community in the early days of the exploration of pyridine derivatives, unremitting research. At that time, many talents dedicated to the expansion of organic synthesis, hoping to obtain new substances for use in medicine and materials.
    After repeated experiments and improved techniques, the method of synthesizing this compound gradually became apparent. With the passage of time, the synthesis process has been perfected day by day, and the yield and purity have been improved. It has emerged in pharmacological research, or is the cornerstone of the creation of new drugs. The historical evolution of this compound is like a pearl in the long river of science, from darkness to brilliance. Thanks to the hard work of countless chemists, today's achievements can be obtained, shining brightly in the field of chemistry.
    Product Overview
    "Description of methyl 3-iodopyridine-4-carboxylic acid esters"
    Methyl 3-iodopyridine-4-carboxylic acid esters, which are important substances involved in my chemical research. Its structure is unique. On the pyridine ring, the iodine atom is cleverly connected to the carboxyl methyl ester. In the reaction, it is often used as a key intermediate.
    Looking at the way of its preparation, it requires fine temperature control and ingredients, and multiple steps of delicate transformation to obtain this pure product. Its chemical activity is quite interesting. The activity of iodine can lead to various nucleophilic substitutions. Carboxyl methyl esters can also undergo hydrolysis and esterification under specific conditions.
    In many fields of chemical research, this substance is like a delicate key, providing the possibility to open novel reaction paths and synthesize unique structural compounds. Its value in organic synthesis cannot be underestimated. When we further study, we may be able to find more wonders and add luster to the field of chemistry.
    Physical & Chemical Properties
    Methyl 3-Iodopyridine-4-Carboxylate is also an organic compound. Its physical properties are mostly solid at room temperature, and its color is close to white. It has a specific melting point, which can be identified and is related to its purity. Looking at its crystal form, its regular structure is also one of its characteristics. Its solubility varies in organic solvents, such as ethanol and acetone, and this property is related to intermolecular forces.
    On its chemical properties, iodine atoms are active and can participate in nucleophilic substitution reactions. Under appropriate conditions, halogen atoms are easily replaced by other groups, causing changes in molecular structure. The carboxyl methyl ester part can be hydrolyzed, especially when it encounters bases, to generate corresponding carboxylic salts and alcohols. The pyridine ring is aromatic and can undergo electrophilic substitution, which varies with its electron cloud distribution and its reactivity check point. All these properties are the key to the study of this compound and the basis for its application in organic synthesis and other fields.
    Technical Specifications & Labeling
    Today there is a chemical substance called Methyl 3 - Iodopyridine - 4 - Carboxylate. Its process specifications and identification (product parameters) are crucial.
    To make this product, it is necessary to follow precise process regulations. From the selection of raw materials, it must be of high quality, with few impurities. The conditions of the reaction, temperature and pressure must be constant and accurate, and a slight difference will affect the quality. The operation of each step also needs to be careful, such as the order of mixing and the length of the reaction, which are all determined.
    As for the identification (product parameters), its physical and chemical properties, such as melting point, boiling point, solubility, etc., need to be detailed for the user to understand. The purity item must be clearly marked, which is the key to measuring the quality of the product. And on the packaging, there should be a striking warning about the dangers of its chemical properties to prevent misuse. In this way, high-quality Methyl 3 - Iodopyridine - 4 - Carboxylate can be obtained, which can be properly used in various fields of chemical industry.
    Preparation Method
    The method of preparing methyl 3-iodopyridine-4-carboxylic acid ester is related to the raw materials and production process, reaction steps and catalytic mechanism. The raw materials are selected from high-purity pyridine derivatives, supplemented by specific halogenating agents and esterification reagents. First, pyridine is used as the base, and iodine atoms are precisely introduced through halogenation, and the reaction temperature and duration are controlled to ensure that iodine is preferentially attacked at the third position of the pyridine ring. Then, it reacts with the carboxylic acid ester reagent, and after esterification, it is successfully connected to the carboxylic acid ester group at the fourth position. During the reaction steps, the pH and reaction atmosphere need to be carefully regulated, or in an inert gas environment, to prevent side reactions from breeding. In terms of catalytic mechanism, high-efficiency metal catalysts are selected to accelerate the reaction process and improve product selectivity by means of their activity checking points. In this way, methyl 3-iodopyridine-4-carboxylic acid esters can be efficiently prepared to meet the needs of chemical production.
    Chemical Reactions & Modifications
    The reaction and change of today's chemistry are based on Methyl 3 - Iodopyridine - 4 - Carboxylate. In the research of chemistry, the goodness of the reaction and the change of the thing are sought. The reaction of Methyl 3 - Iodopyridine - 4 - Carboxylate is related to various factors. If the conditions are different, such as temperature and amount of agent, it should be different.
    If you want to change its nature, you must study its rationale. Either adjust the situation of the reaction, or make it easy to use the agent to promote it to the desired direction. This is all up to the researcher to observe and think carefully, and introduce new ones. Make the reaction smooth and good, and the sex must be adjusted appropriately. In the karma of transformation, it is the most important thing to study unremittingly, and then you can make progress.
    Synonyms & Product Names
    Today there is a thing called Methyl 3 - Iodopyridine - 4 - Carboxylate. The synonyms and trade names of this thing are also of concern to us. Its synonyms may have various nicknames to meet the needs of different situations. And the trade name is related to its logo in the market.
    This compound is an important research corner in the field of chemistry. The variety of synonyms is like a list of stars, each has its own use. Due to academic heritage or regional differences, the names of synonyms are elegant. The trade names are like the emblems of merchants, which are eye-catching and unique, and are known to everyone.
    Although there are many names for this thing, in essence, they all point to the same entity. We chemical researchers need to clarify the relationship between its synonyms and trade names in order to be accurate and not confused when researching and applying. In this way, we must deeply explore the characteristics and uses of this thing, and contribute to the development of chemistry.
    Safety & Operational Standards
    Methyl 3 - Iodopyridine - 4 - Carboxylate is also used to dispose of the material. Its safety and operation are of paramount importance.
    Anyone who comes into contact with this product must first be informed of its properties. This product may be dangerous to a certain extent, and it is necessary to keep it safe during operation.
    The place where the operation is carried out is convenient to be good, so as to avoid its steaming. The person who operates the product should take appropriate precautions, such as clothing, gloves, and eyes, to prevent the skin from catching the eyes.
    If the skin is accidentally contaminated, immediately wash it with a lot of water, and according to the situation, seek medical treatment. If it enters the eyes, it needs to be washed with physiological water or water immediately, and it cannot be delayed. It should be treated as soon as possible.
    It is also necessary to be careful when it is in storage. It should be placed in a dry, dry and transparent place, and a source of ignition and oxidation. The container that is stored must be well sealed to prevent leakage.
    After use, it should not be placed on its contents. It should be properly handled according to the relevant conditions to avoid contamination of the environment.
    In addition, the safe operation of Methyl 3 - Iodopyridine - 4 - Carboxylate must be followed, so as to ensure the safety of the operator and not cause harm to the environment.
    Application Area
    Today, there is a thing called Methyl 3-Iodopyridine-4-Carboxylate, which is quite promising in various application fields. In the field of pharmaceutical research and development, it can be used as a key intermediate to help create new drugs, cure various diseases, and save people from diseases. In the field of material science, it can improve the material properties, make the material tough and specific, and is widely used in equipment manufacturing and many other aspects. In the context of chemical production, it can be used as a reaction raw material to derive a variety of fine chemical products to meet the diverse needs of the world. Its wide application and deep impact cannot be underestimated, and it is expected to open up new paths for various fields, benefit and benefit people.
    Research & Development
    In recent years, the genus of methyl 3-iodopyridine-4-carboxylate has been studied, which is related to research and progress, and is very important. This compound has a unique chemical structure and has great potential in the field of organic synthesis.
    Researchers have dedicated themselves to exploring the synthesis method, hoping to optimize the process and improve the yield. At first, they tried a variety of paths, or due to harsh conditions, or due to complex side reactions, the progress was difficult. However, everyone was unyielding and tried repeatedly, and finally obtained an exquisite method, which can be prepared with high efficiency.
    At the same time, they also studied its reaction characteristics, hoping to expand the scope of application. After unremitting efforts, we have made progress in drug research and development, materials science, etc., and are expected to contribute to the entry of related fields, leading a new path for future research and development, and opening up a vast world.
    Toxicity Research
    Taste the industry of chemistry now, in the depth of the investigation of various substances. Now on Methyl 3-Iodopyridine-4-Carboxylate this substance, the study of its toxicity is crucial.
    When studying its toxicity, the first to observe its chemical properties. This substance has a unique structure. The combination of iodine, pyridine and carboxyl esters may cause toxic changes. In living organisms, or involved in chemical reactions, causing damage to cells.
    Furthermore, observe its state in the environment. If it escapes from the outside, or is absorbed by water sources and soil, and then enters the biological chain. After biological enrichment, its virulence or drama endangers all living things.
    Experimental testing is also indispensable. Taking animals as models, the relationship between dose and response was explored to clarify its acute and chronic toxicity, and regulations were made for protection and application to ensure the safety of humans and the environment.
    Future Prospects
    Fuchthyl 3-iodopyridine-4-carboxylic acid ester is a chemical that I have dedicated myself to exploring. Looking forward to the future, it will shine in the field of pharmaceutical creation. With its unique structure, it may become the cornerstone of new drugs to heal all kinds of diseases.
    In the field of materials science, it is also expected to emerge. With its characteristics, it may be able to develop novel functional materials, opening up new avenues for electronics, optics and other industries.
    Our scientific researchers should do their best to explore its potential. With accurate experiments and profound thinking, we hope to make this compound shine in the future, contribute to human well-being, and live up to the mission and expectations of scientific research.
    Historical Development
    In the past, in the field of organic chemistry, there was a thing called Methyl 3 - Iodopyridine - 4 - Carboxylate, and its origin was unknown to everyone. At that time, the sages of chemistry studied the properties of substances, hoping to expand the frontier of cognition. At the beginning, the synthesis method was not good, the yield was very small, and the quality of it was analyzed, and it was very difficult.
    However, the determination of scholars, unremitting research. After years of work, the synthesis method has gradually refined, and the yield has also increased. Therefore, this substance has gradually become useful in the process of organic synthesis. Or as an intermediate to help other substances; or in the research and development of medicine, it has emerged. The course of its development, although not smooth, but the efforts of all the sages, finally let it occupy a place in the forest of chemistry, for the follow-up research, paving the cornerstone, waiting for the future, more ability.
    Product Overview
    Today there is a compound called Methyl 3-Iodopyridine-4-Carboxylate. It is an organic compound with a unique structure. Looking at its structure, on the pyridine ring, the third position is connected to the iodine atom, and the fourth position is connected to the carboxylic acid methyl ester group. This substance has a wide range of uses in the field of organic synthesis. It can be used as a key intermediary to prepare a variety of biologically active substances. Its properties are stable, but under specific reaction conditions, iodine atoms and ester groups can participate in many chemical reactions to realize the transformation and modification of functional groups. With its special chemical properties, it can provide an effective way to create novel drugs, functional materials, etc. It is of great value in chemical research and industrial production, and cannot be ignored in the field of chemistry.
    Physical & Chemical Properties
    Methyl 3-Iodopyridine-4-Carboxylate is also an organic compound. Its physical properties, at room temperature, are solid, white and pure in color, like a fine powder, with a slight odor. Its melting point is moderate, and it melts into a liquid within a specific temperature range. This property is conducive to manipulation in many experiments and industrial processes.
    In terms of chemical properties, this compound has certain activity. Because it contains iodine atoms and carboxyl methyl ester groups, it is easy to participate in nucleophilic substitution reactions. The iodine atom is active and can be replaced by many nucleophilic reagents. Carboxyl methyl esters can be hydrolyzed and alcoholized under suitable conditions, and a variety of compounds with different functions can be derived. It has great application potential in drug synthesis, materials science and other fields.
    Technical Specifications & Labeling
    Today there is a product called Methyl 3 - Iodopyridine - 4 - Carboxylate. To clarify its technical specifications and identification (product parameters), it is necessary to study the school in detail. The preparation method needs to follow precise steps. The raw materials used must meet the requirements of high accuracy. When reacting, various parameters such as temperature and duration are all key, and a slight error will damage the quality. In its identification, information such as composition and purity can be clearly identified, which is a proof of quality. The technical specifications and identification of this product are related to practical efficiency and safety, and must be strictly treated in order to obtain good products to meet all needs.
    Preparation Method
    To prepare Methyl 3 - Iodopyridine - 4 - Carboxylate, the raw materials, production process, reaction steps and catalytic mechanism are the key. First, take methyl pyridine - 4 - carboxylate as the raw material, and use an appropriate catalyst to react with the iodine substitution reagent under a specific temperature and pressure environment. This reaction requires precise temperature control, observation of its reaction process, and timely adjustment of conditions.
    At the beginning of the reaction step, mix the raw materials and the catalyst, slowly heat up to the required temperature for the reaction, so that the two fully blend and react. When the reaction gradually stabilizes, continue to observe the changes of the reactants. If there are side reactions, quickly adjust the reaction conditions to maintain the purity of the product. The catalytic mechanism of
    relies on the power of the catalyst to reduce the activation energy of the reaction and promote the efficient conversion of raw materials into products. The selection of suitable catalysts can greatly improve the reaction rate and yield. In this way, through fine regulation of raw materials, processes, steps and catalytic mechanisms, it is expected to obtain high-purity Methyl 3 - Iodopyridine - 4 - Carboxylate.
    Chemical Reactions & Modifications
    To taste the wonders of chemical industry, it is essential to change substances, react and modify them. In this word, Methyl 3 - Iodopyridine - 4 - Carboxylate.
    Its chemical reaction is like yin and yang sympathetic, or in contact with nucleophiles, halogen atoms are translocated, and the structure is changed, just like the twist of the universe, to obtain new derivatives. Or under specific temperature, pressure and catalyst conditions, the reaction of carboxylation occurs, expanding the carbon chain and enriching its properties.
    As for modification, different groups can be introduced to adjust its polarity and solubility. If the hydrocarbon group is connected to increase its fat solubility; if it is combined with nitrogen-containing heterocycles, it will change its electron cloud distribution and affect its activity and stability. In this way, in the fields of drug research and development, material creation, etc., it can display its extraordinary capabilities to meet the needs of all parties and explore the endless wonders of chemical industry.
    Synonyms & Product Names
    Methyl 3-iodopyridine-4-carboxylate, the synonym and trade name of this substance, is also the focus of our chemical research. There are many synonyms, all of which are terms describing the characteristics and structure of this substance. Trade names vary according to different manufacturers and markets.
    In the field of chemistry, exploring its synonyms can help us more accurately understand the essence of this substance. Or according to its chemical structure, reaction characteristics, or according to its use and source, many synonyms can be derived. The existence of trade names is designed to circulate in the market, making it easy for consumers and users to identify and choose.
    Methyl 3-iodopyridine-4-carboxylate is used in many fields due to its unique chemical properties. Studying its synonyms and trade names can enable us to communicate information more clearly and accurately in academic exchanges and industrial applications, avoid confusion, and then promote the development of chemical research and related industries.
    Safety & Operational Standards
    About "Methyl 3 - Iodopyridine - 4 - Carboxylate" Product Safety and Operation Specifications
    The husband of "Methyl 3 - Iodopyridine - 4 - Carboxylate" is an important product in chemical research. During its experimental operation and application, safety and standardization are of the utmost importance.
    First word safety. This product has certain chemical activity, or poses a potential danger to the human body and the environment. Experimenters should always keep protective equipment, such as gloves, goggles, gas masks, etc., to prevent contact with the skin, eyes, and inhalation of its volatile gas. In case of accidental contact, rinse with plenty of water as soon as possible, and seek medical treatment according to the situation. When storing, it should be placed in a cool, dry and well-ventilated place, away from fire and heat sources, and stored separately from oxidants and reducing agents to avoid chemical reactions and dangerous things.
    Times and operating specifications. Before the experimental operation, the experimenter must know the relevant chemical properties and reaction mechanism in detail, and make a comprehensive plan in advance. During the operation, measure accurately, and react according to the established steps and conditions. Do not change at will. The experimental equipment needs to be clean and dry to ensure the accuracy of the experimental results. After the reaction, properly dispose of the experimental waste. It should not be discarded at will. It should be sorted and disposed of in accordance with environmental protection regulations to avoid polluting the environment.
    In conclusion, in the research and application of "Methyl 3 - Iodopyridine - 4 - Carboxylate", strict adherence to safety and operating standards can achieve the purpose of research and ensure the safety of personnel and the environment.
    Application Area
    In the field of medicine, it can be used as the key raw material for synthesizing good medicines, and it can help physicians make healing agents to solve the problems of many people. In the field of materials, it can also be the basis for the research and development of novel materials, making the materials special, or tough and abnormal, or excellent conduction. And in the process of chemical synthesis, it provides opportunities for many reactions, allowing substances to be transformed at will, expanding the boundaries of the chemical industry, introducing new chapters in the industry, and in various application fields, all of them show their extraordinary capabilities, contributing to the development of this world.
    Research & Development
    In recent years, we have studied methyl 3-iodopyridine-4-carboxylic acid ester. In the field of organic synthesis, it is a key intermediate and has a wide range of uses. We study the synthesis path, improve the old method, and increase its yield and purity. The old method, or the raw materials are rare, or the steps are cumbersome, and the yield is not good. Our innovative method starts with the common pyridine, and through halogenation and esterification steps, we obtain this product. The new method has mild conditions, easy operation, easy availability of raw materials, and cost control. The reactivity of this substance was also explored, and it performed well in the coupling reaction. It can be used to connect different groups to expand its application. The research and development of methyl 3-iodopyridine-4-carboxylate has a broad prospect, which is expected to add new colors to the field of organic synthesis and help the development of new materials and new drugs.
    Toxicity Research
    The toxicity of methyl 3-iodopyridine-4-carboxylic acid ester is under investigation. This substance is a new product of chemistry. Its properties are unknown, and it is related to the safety of use. Therefore, it is studied.
    Take a few of this substance and test it by various methods. Observe its combination with other substances and its changes under different circumstances. Observe the response of the test substance, such as changes in shape and color, and the opposite of the organism.
    Initial test, no significant difference was found. However, continued research, under specific circumstances, there may be concerns. Although no signs of severe toxicity were found, trace accumulation, or potential danger. It is necessary to be careful, study its nature in detail, clarify its harm, and ensure the safety of the user to avoid the danger of being cute.
    Future Prospects
    Today there is a thing called Methyl 3 - Iodopyridine - 4 - Carboxylate, and I have been studying it for a long time. Looking at this compound, its structure is exquisite and it contains infinite possibilities. Although I know it today, it is only its appearance, but I look forward to the future.
    It is expected that in the future, after repeated experiments and fine investigation, its unique reaction mechanism may be able to be revealed, and it will shine in the field of organic synthesis. Or it can be applied to the creation of novel drugs to relieve the pain of patients; or it can help the research and development of materials to generate new materials with excellent performance.
    I firmly believe that with time and dedication, this compound will be able to appear like a pearl in the world of chemistry, open up a new realm, and achieve extraordinary achievements. The future prospects are bright and promising.
    Historical Development
    Taste the field of chemical industry and explore endlessly. There is a thing called Methyl 3-Iodopyridine-4-Carboxylate, and its birth can also be traced. At the beginning, the sages found clues in the micro-end, and with exquisite methods, they started the road of synthesis. At that time, the skills were not yet mature, but those who were determined were unremitting and tried again and again.
    Years pass, and the techniques are gradually refined. From the crude at the beginning to the delicate in the follow-up, every step is soaked in hard work. Researchers seek the truth between bottles and cans. As time passes, the synthesis method becomes increasingly complete, and the purity and yield of this compound increase.
    Looking at its journey, it is like a journey of stars, from weak light to shining. From less to more, from simple to complex, it has carved a unique mark in the long river of chemical industry, becoming the development chapter of Methyl 3-Iodopyridine-4-Carboxylate.
    Product Overview
    Today there is a product called Methyl 3-Iodopyridine-4-Carboxylate. This is a key raw material for organic synthesis and is widely used in the fields of medicine and pesticides. It is a colorless to light yellow liquid with a special odor. Boiling point, melting point and other physical properties are stable, and under specific temperature and pressure conditions, the properties are particularly good.
    Preparation of this product often follows a specific chemical path and is obtained through multiple steps. In the reaction, it is necessary to precisely control the temperature, time, proportion of reactants and other factors to obtain high-purity products.
    Because of its great significance in industrial production and scientific research, our chemical researchers should devote themselves to research and strive to refine the preparation process and improve the quality of the product, so as to promote its wider application and benefit the world.
    Physical & Chemical Properties
    "Physical Properties of Methyl 3-Iodopyridine-4-Carboxylic Acid Ester"
    Methyl 3-iodopyridine-4-carboxylic acid ester, its color is light yellow, like a crystalline powder, under normal conditions, quite stable. Its melting point is about [X] ° C, and it gradually melts when heated, which is one of its physical characteristics.
    In terms of chemical properties, this substance has certain reactivity. Its iodine atom is active and easy to be replaced by nucleophiles, and can participate in many organic synthesis reactions. The existence of the pyridine ring gives it a certain alkalinity, which can react with acid substances to form corresponding salts. And its carboxylic acid ester groups can be decomposed into corresponding carboxylic acids and alcohols under hydrolysis conditions. In the field of organic synthesis, this property is often used to construct more complex compound structures. In short, the physical and chemical properties of methyl 3-iodopyridine-4-carboxylic acid esters lay an important foundation for their application in organic synthesis and other fields.
    Technical Specifications & Labeling
    This product is methyl 3-iodopyridine-4-carboxylate. Its process specifications and identification (product parameters) are the key. To make this product, follow a rigorous method. The material selection must be fine, the ratio is appropriate, the operation is in sequence, and there should be no difference.
    As far as the identification is concerned, the product parameters must be detailed, such as the purity geometry, the impurity content, and the physical and chemical properties should be clear. This can make its properties and uses clear to everyone at a glance. Strict adherence to process specifications and accurate identification can preserve the high quality of methyl 3-iodopyridine-4-carboxylate, and it can be suitable for all applications and play its effect.
    Preparation Method
    The method of preparing methyl 3-iodopyridine-4-carboxylic acid esters is related to the raw materials and production process, reaction steps and catalytic mechanism. The raw materials are taken from pyridine derivatives, supplemented by iodide and specific esterification reagents. First, the pyridine derivative and iodide are catalyzed by a certain catalyst in a suitable solvent, and the temperature is controlled and stirred. After the reaction steps of nucleophilic substitution, the iodine atom is connected to the pyridine ring. Then, the esterification reagent is added, the reaction conditions are adjusted, and the esterification reaction is carried out, and then the methyl 3-iodopyridine-4-carboxylic acid ester is formed. In this process, precise temperature control, selection of suitable solvents and catalysts are related to the reaction rate and product purity. The catalytic mechanism is that the catalyst activates the reactants, reduces the reaction energy barrier, and promotes the efficient progress of the reaction. Precise control of each reaction step is the key to producing high-purity products.
    Chemical Reactions & Modifications
    Methyl 3-iodopyridine-4-carboxylic acid ester is an important matter in chemical reaction and modification. The mechanism of its reaction needs to be explored in detail. Or by nucleophilic substitution, the iodine atom is replaced by other groups, and then its properties are changed.
    The choice of nucleophilic reagents is crucial. If a suitable amine is used as an agent, a nitrogen-containing group can be introduced to make the substance have other activities. Or with nucleophilic alcohols, the ester group can be changed to change its solubility and reactivity. When
    is modified, the stability and functionality of the product should be considered. By adjusting the reaction conditions, such as temperature, solvent and catalyst, the desired product can be obtained. And this product may have extraordinary uses in the fields of medicine and materials, so chemical reactions and modifications need to be carefully studied to expand its application.
    Synonyms & Product Names
    Today there is a thing called Methyl 3-Iodopyridine-4-Carboxylate. The synonymous name of this thing and the trade name are related to the importance of our research. Its synonymous name may come from its chemical structure characteristics to accurately describe its composition and composition. The trade name is mostly for the convenience of market circulation, hoping to make it easy to remember and make it known to everyone.
    I am equal to the complexity of common synonymous names in research. Or because of academic inheritance, the words used by various schools are slightly different; or because the research focuses on different, but the names are different. As for the trade name, merchants take wonderful names to show their characteristics and expand their sales. However, no matter the synonymous name or the trade name, it is the truth of this thing. Our chemical researchers should carefully observe the differences and use them accurately to avoid confusion and errors in the research. This has great significance for the exploration of chemistry and the application of industry.
    Safety & Operational Standards
    About Methyl 3 - Iodopyridine - 4 - Carboxylate Product Safety and Operation Specifications
    F Methyl 3 - Iodopyridine - 4 - Carboxylate, chemical products are also. When preparing, storing and using it, strict safety and operation practices should be followed to ensure the safety of people and the environment.
    When preparing, all raw materials and reagents should be accurately measured and properly mixed. Experimental equipment must be clean and dry to prevent impurities from mixing, causing reaction deviation, or even causing danger. Operators must wear protective equipment, such as goggles, gloves, lab clothes, etc., to avoid direct contact with skin and eyes.
    Storage rules, this product should be placed in a cool, dry, well-ventilated place, away from fire and heat sources. Do not store with oxidizing agents, reducing agents, etc. to prevent chemical reactions and hidden dangers. Containers should be tightly sealed to prevent volatilization and leakage.
    When using, operate in a fume hood to ensure air circulation and remove harmful gases that may be generated. If it comes into contact with the skin, rinse with plenty of water immediately, followed by soap. If it enters the eyes, rinse immediately with flowing water or normal saline, and seek medical attention immediately.
    Disposal should be in accordance with relevant laws and regulations, and should not be dumped at will. It must be collected by classification and handed over to professional institutions for treatment, free of pollution environment.
    In conclusion, the safety and operation specifications of Methyl 3 - Iodopyridine - 4 - Carboxylate are of great significance. From preparation to disposal, all aspects should not be ignored. Only by adhering to the norms can we avoid disasters and ensure the smooth operation of the experiment, the safety of personnel and the environment.
    Application Area
    Methyl 3 - Iodopyridine - 4 - Carboxylate, the best product of chemistry. Its application field is quite vast. In the field of pharmaceutical creation, it can be a key intermediate, help to develop novel drugs, or have great effect on the treatment of specific diseases. With its unique chemical structure, it can precisely interact with molecules in the body to achieve the purpose of treatment. In the field of materials science, it has also emerged, or it can be specially treated for the preparation of materials with specific properties, such as outstanding optical and electrical properties, which contribute to material innovation. In the process of organic synthesis, it is often used as an important building block to help chemists build complex organic molecules, expand the boundaries of organic chemistry, and promote the continuous progress of this field, benefiting many industries.
    Research & Development
    I have been studying methyl 3-iodopyridine-4-carboxylic acid ester for a long time. This compound has exquisite structure and unique properties, and has great potential in the field of organic synthesis.
    At the beginning, I explored the method of its synthesis. After various attempts, the ratio of raw materials and reaction conditions were carefully studied. Or the temperature is slightly different, or the solvent is different, the effect of the product will be very different. However, unremitting research, I finally got a better method, and the yield gradually increased.
    Then, explore its properties. In different media, observe its stability and reactivity. It is clear where it can react with, and where it can maintain its own stability. This is the cornerstone for future applications.
    Now, look to the future. Methyl 3-iodopyridine-4-carboxylate is expected to shine in the fields of medicine and materials. We should continue to study it to tap more potential, promote its development, and contribute to the progress of science.
    Toxicity Research
    The nature of taste and smell is related to its use and human feelings. Now look at Methyl 3-Iodopyridine-4-Carboxylate, the study of its toxicity is quite important.
    Those who are toxic may harm the body of the living being or disrupt its physiological order. Study the toxicity of this thing, when it encounters with living things, observe the various changes that occur. If it enters the body, it can explore its path of travel and affect the ability of the viscera.
    In the context of experiments, try it with various living things, observe the differences in its representation, and observe its physiological changes. Only by recording it in detail and analyzing its cause and effect can we understand the intensity of its toxicity and the scope involved. This research is also to ensure the safety of all living beings, avoid its harm and use its benefits, so that this chemical substance is in harmony with the Tao, follows the reason, and does not go against the life of living beings.
    Future Prospects
    Methyl 3-iodopyridine-4-carboxylic acid ester is also an important substance in organic synthesis. This compound has a delicate structure and specific properties, and has great prospects for future research and application.
    In today's world, science and technology are changing, and chemical research is also advancing rapidly. Methyl 3-iodopyridine-4-carboxylic acid ester is used in the field of drug research and development, and may become the basis for new drugs, cure various diseases, and save patients from diseases. In the genus of materials science, it may also be the key to creating novel materials, endowing materials with specific properties and applying them to electronics and energy.
    Although the current understanding of it is still limited, in time, with the diligent study of our researchers, we will be able to understand its mysteries and expand its application. In the future, methyl 3-iodopyridine-4-carboxylate can shine brightly and add brilliance to human well-being, which is the earnest hope of our chemical researchers.
    Where to Buy Methyl 3-Iodopyridine-4-Carboxylate in China?
    As a trusted Methyl 3-Iodopyridine-4-Carboxylate manufacturer, we deliver: Factory-Direct Value: Competitive pricing with no middleman markups, tailored for bulk orders and project-scale requirements. Technical Excellence: Precision-engineered solutions backed by R&D expertise, from formulation to end-to-end delivery. Whether you need industrial-grade quantities or specialized customizations, our team ensures reliability at every stage—from initial specification to post-delivery support.
    Frequently Asked Questions

    As a leading Methyl 3-Iodopyridine-4-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 Methyl 3-iodopyridine-4-carboxylate?
    Methyl-3-iodopyridine-4-carboxylic acid esters are important compounds in the field of organic synthesis. They have a wide range of uses, first in the field of medicinal chemistry. In this field, they are often used as key intermediates to create various biologically active drug molecules. For example, through a series of chemical reactions, a drug skeleton with a specific structure can be constructed. By modifying the substituents on the pyridine ring, the interaction between the drug and the target can be adjusted to improve the efficacy and reduce side effects.
    Furthermore, in the field of materials science, methyl-3-iodopyridine-4-carboxylic acid esters also have unique uses. It can participate in the preparation of functional organic materials, such as luminescent materials, conductive materials, etc. Its special molecular structure endows the material with specific optical and electrical properties, providing the possibility for the development of new high-performance materials.
    In addition, in the study of organic synthesis methodologies, this compound is also often used as a substrate. Chemists use this to explore novel chemical reaction pathways and strategies, such as palladium-catalyzed coupling reactions. Through such reactions, effective connection of pyridine rings with other organic groups can be achieved, expanding the structural diversity of organic molecules, and contributing to the development of organic synthesis chemistry. In conclusion, methyl-3-iodopyridine-4-carboxylic acid esters play an indispensable role in many fields and contribute significantly to the advancement of related scientific fields.
    What are the synthetic methods of Methyl 3-iodopyridine-4-carboxylate?
    There are several common methods for synthesizing methyl 3-iodopyridine-4-carboxylic acid esters. One is to start with pyridine-4-carboxylic acid, and first go through the method of esterification, so that it can be esterified with methanol under the catalysis of acid, such as concentrated sulfuric acid or p-toluenesulfonic acid, etc., to obtain methyl pyridine-4-carboxylic acid ester. Then, the product is added to a suitable solvent, such as dichloromethane or chloroform, under the action of iodine substitution reagents, such as N-iodosuccinimide (NIS) or the combination of iodine and oxidizing agent, at mild temperatures, such as room temperature to about 50 ° C, after a certain period of time, the purpose of iodine substitution can be achieved, and methyl 3-iodopyridine-4-carboxylate is obtained.
    Furthermore, starting from 3-halogenated pyridine-4-carboxylic acid esters, if the 3-halogen atom is chlorine or bromine, with an iodizing agent, such as potassium iodide, etc., under the help of a phase transfer catalyst, such as tetrabutylammonium bromide, in a suitable solvent, such as acetone or acetonitrile, when heated and refluxed for several times, the halogen atom is replaced by an iodine atom, and the final product is obtained.
    Or start with the construction of the pyridine ring, with suitable nitrogen-containing, carbonyl-containing and halogenated small molecules as raw materials, through multi-step cyclization reaction, the pyridine ring structure is first formed, and then methyl ester groups and iodine atoms are introduced. Although there are many steps in this path, if the design is exquisite, it can also achieve the purpose of synthesis. During synthesis, attention should be paid to the control of reaction conditions, the selection of solvents and reagents, and the purification of each step of the reaction, so as to obtain better yield and purity.
    What are the physical properties of Methyl 3-iodopyridine-4-carboxylate?
    Methyl 3-iodopyridine-4-carboxylate is an organic compound with unique physical properties. Its appearance is usually a crystalline solid, and its color may be white to light yellow. This is due to the specific arrangement and interaction of molecular structures, light reflection and absorption characteristics.
    When it comes to the melting point, the melting point of this compound is about [X] ° C, and the melting point is determined by intermolecular forces, such as van der Waals force, hydrogen bond, etc. Its molecular structure is specific, and the force is stable, which requires specific temperatures to overcome and reach the melting point state change.
    In terms of boiling point, the boiling point of methyl 3-iodopyridine-4-carboxylate is about [X] ° C. The boiling point is closely related to the intermolecular force, and the force is strong. Gasification requires more energy and the boiling point is higher. The molecular force of this compound makes the boiling point in the corresponding range.
    In terms of solubility, it has a certain solubility in organic solvents such as dichloromethane and chloroform. Due to the principle of "similar miscibility", the compound matches the polarity of organic solvent molecules and can interact and disperse uniformly. However, the solubility in water is poor, because its molecular polarity is very different from water, it is difficult to form effective interactions.
    Density is also an important physical property. The density of methyl 3-iodopyridine-4-carboxylate is about [X] g/cm ³. The density reflects the unit volume mass of the substance and is determined by the molecular weight and the degree of packing compactness. The molecular mass and structural stacking characteristics of the compound make the density in this numerical range.
    In addition, the stability of the compound is acceptable under general conditions, but in case of specific chemical substances such as strong oxidizing agents, strong acids, and strong bases, or extreme conditions such as high temperature and light, chemical reactions may occur and cause structural changes.
    These physical properties of methyl 3-iodopyridine-4-carboxylate are of great significance in the fields of organic synthesis and drug development. Researchers can use this to understand its behavioral characteristics and design more effective synthesis routes and application methods.
    What are the chemical properties of Methyl 3-iodopyridine-4-carboxylate?
    Methyl 3-iodine-pyridine-4-carboxylate is a genus of organic compounds. It has unique chemical properties and is of great significance to organic synthesis.
    From the structural point of view, the pyridine ring is its core, with iodine atom at 3 position and carboxyl methyl ester group at 4 position. This structure gives it specific chemical activity. Iodine atoms have high activity. Due to their electronegativity differences, C-I bonds have a certain polarity and are prone to nucleophilic substitution reactions. In many organic reactions, iodine atoms can be replaced by nucleophilic reagents, such as reacting with compounds containing hydroxyl groups, amino groups and other nucleophilic groups, thereby forming new carbon-heteroatom bonds, which lays the foundation for the synthesis of complex organic molecules.
    Carboxymethyl ester groups are also active. Ester groups can undergo hydrolysis reactions, and can be converted into corresponding carboxylic acids or carboxylic salts under the catalysis of acids or bases. When alkali catalyzes hydrolysis, the reaction rate is faster, and 3-iodopyridine-4-carboxylic acids and methanol are generated. This carboxylic acid can further participate in esterification, amidation and other reactions to expand the derivatization ability of compounds. The presence of the
    pyridine ring makes the compound weakly basic and can react with acids to form salts. Due to its conjugation system, the pyridine ring can participate in the electron transfer process and affect some redox reactions. Methyl 3-iodopyridine-4-carboxylate can be used as a key intermediate in the field of organic synthesis, and organic molecules with biological activity or special functions can be synthesized through rational design of reaction pathways.
    What is the price of Methyl 3-iodopyridine-4-carboxylate in the market?
    The price of methyl 3-iodopyridine-4-carboxylate in the market is difficult to determine. The price often changes due to various factors.
    First, it is related to the output. If the output of this product is abundant and the supply exceeds the demand, the price may become flat. On the contrary, if the output is scarce and the supply exceeds the demand, the price will rise. Second, it depends on the quality. Those with high quality are expensive; if the quality is slightly inferior, the price may be lower. Furthermore, market demand is also the key. If the demand for it is strong at a certain time, the price will rise; if the demand is weak, the price will not improve.
    In the past, in the world of "Tiangong Kaiwu", the price of various materials was affected by the origin, season, supply and demand. The same is true for methyl 3-iodopyridine-4-carboxylate. Its price may fluctuate due to the difficulty of preparation process and the cost of raw materials. To know its exact market price, you must ask the merchants specializing in this chemical and the chemical raw material trading platform in detail to get a more accurate price.