Ethyl 3-(4-Iodophenyl)-3-Oxopropanoate

Fengxi Chemical

Specifications

HS Code	459659
Chemical Formula	C11H11IO4
Molar Mass	336.107 g/mol
Appearance	Typically a solid (description may vary)
Solubility In Water	Low solubility (organic esters generally have low water solubility)
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Boiling Point	Estimated based on similar esters, likely in a certain range (exact value may require experimental determination)
Melting Point	Specific melting point value needs experimental measurement
Density	Density value depends on temperature and requires experimental determination
Ir Spectrum Characteristics	Characteristic absorption peaks related to carbonyl, ester, and iodine - containing groups
H Nmr Spectrum Characteristics	Peaks corresponding to different hydrogen environments in the molecule
Chemical Formula	C11H11IO4
Molar Mass	336.11 g/mol
Appearance	Typically a solid (description may vary)
Solubility In Water	Low (organic esters often have low water solubility)
Solubility In Organic Solvents	Soluble in common organic solvents like ethanol, dichloromethane
Odor	May have a characteristic ester - like odor
Stability	Stable under normal conditions, but may react with strong oxidizing or reducing agents
Chemical Formula	C11H11IO3
Molar Mass	318.11 g/mol
Appearance	Solid (usually white to off - white)
Melting Point	80 - 84 °C
Solubility In Water	Insoluble
Solubility In Organic Solvents	Soluble in common organic solvents like dichloromethane, ethyl acetate
Purity Typically	Can be obtained in high purity (e.g., 95%+ in commercial products)

As an accredited Ethyl 3-(4-Iodophenyl)-3-Oxopropanoate 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 3-(4 - iodophenyl)-3 - oxopropanoate in a sealed, labeled chemical - grade bottle.
Storage	Ethyl 3-(4-iodophenyl)-3-oxopropanoate should be stored in a cool, dry place, away from heat sources and direct sunlight. Keep it in a well - sealed container to prevent moisture absorption and exposure to air, which could potentially lead to chemical degradation. Store it separately from incompatible substances, like strong oxidizing agents, to avoid any unwanted reactions.
Shipping	Ethyl 3-(4-iodophenyl)-3-oxopropanoate is shipped in well - sealed, corrosion - resistant containers. It's handled with care due to its chemical nature, and shipped in accordance with hazardous chemical transport regulations.

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General Information

Historical Development

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is a crucial compound in the field of organic synthesis. In the past, since the dawn of organic chemistry, chemists have devoted themselves to the exploration of such iodine and carbonyl ester compounds. At that time, due to technical and cognitive limitations, it was difficult to synthesize this compound. However, with the passage of time, chemical skills have become more and more exquisite, and the understanding of reaction mechanisms has become more and more profound. First, chemists tried a variety of basic synthesis paths to gradually optimize the reaction conditions. After long-term research and numerous experimental improvements, a more efficient and stable synthesis method has been found, resulting in a significant increase in the yield and purity of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate, and its application in organic synthesis and related scientific research fields has become increasingly widespread.

Product Overview

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an important product of organic synthesis. Its compound is an ester, containing iodophenyl and carbonyl groups in the molecule, and has a unique structure. This compound can be prepared through specific organic reactions, such as iodophenyl derivatives and carbonyl esters, obtained through condensation and other reaction pathways. In the field of organic synthesis, it is often a key intermediate and can participate in many reactions to construct complex organic molecules. Due to the activity of iodine atoms in its structure, it can undergo reactions such as nucleophilic substitution to introduce other functional groups. The presence of carbonyl also provides a variety of activity check points for reactions, or participates in addition and condensation. In the fields of medicinal chemistry and materials science, it has potential application value and is an important object of organic synthesis research.

Physical & Chemical Properties

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an important compound in organic synthesis. In terms of physical properties, it is mostly colorless to light yellow liquid at room temperature, with a specific odor and certain volatility. The boiling point is in a specific temperature range to ensure its phase stability under specific conditions.
From the perspective of chemical properties, the carbonyl and iodine atoms in this compound make it significantly active. Carbonyl can participate in reactions such as nucleophilic addition, while iodine atoms can undergo substitution reactions under appropriate conditions and interact with many nucleophilic reagents. This property makes Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate a key intermediate in the construction of complex organic molecular structures, and has important application value in the fields of medicinal chemistry and materials science.

Technical Specifications & Labeling

There is a product today called Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. To clarify its technical specifications and labels (commodity parameters), it is necessary to explore in detail.
The technical specifications of this product are related to its chemical composition and preparation method. Its chemical structure is established, and the preparation needs to follow a precise method. The proportion of materials used and the reaction conditions must be appropriate. Such as reaction temperature, duration, and catalyst selection are all key.
As for the logo (commodity parameters), it includes the appearance of the state, or the genus of color and shape; the purity geometry is the quality of the product; there are also relevant physical constants, such as melting point, boiling point, etc., which can be used as evidence for identification. In this way, the technical specifications and identification (commodity parameters) of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate can be clarified, which is of great benefit to research and application.

Preparation Method

To prepare Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate, its raw materials and production process, reaction steps, and catalytic mechanism are the key.
First take an appropriate amount of 4-iodobenzoic acid, dissolve it in an alcohol solvent, add a suitable catalyst, heat it up to a specific temperature, and carry out the esterification reaction. When the reaction is smooth, add an acetylation reagent, control the temperature and adjust the reaction time to promote the accurate integration of the acetyl group. In this step, the reaction needs to accurately grasp the ratio and temperature of the reagent, otherwise it will affect the yield and purity.
After the reaction is completed, the product is purified through cooling, extraction, distillation and other steps. When cooling, pay attention to the rate to avoid poor crystallization. During the extraction process, choose the appropriate extractant to ensure effective separation. In the distillation process, the pressure and temperature are controlled to obtain pure Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. In this way, a good method for preparing this substance is obtained.

Chemical Reactions & Modifications

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate The transformation and change of this thing, the ancient alchemy, and today's research are all involved. In the past, based on the ancient law, the practice of transformation and adaptation was based on the ancient law, although it was effective, there were many problems. The rate of transformation and adaptation is often difficult to satisfy, and there are many by-products, so that pure products are difficult to mention.
Today, all researchers think about changes and seek innovation, and study in detail the method of transformation and adaptation. Change its medium, adjust its temperature and pressure, in order to promote its response speed and increase its yield. After repeated trials and obtained a good method, the effect of transformation and adaptation is quite advanced, the yield is increased, and the by-product is gradually reduced. Such a change has made the preparation of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate more refined, and it is effective in both work and research. From this point of view, the technique of transformation and adaptation can be applied more and more widely and benefit more and more.

Synonyms & Product Names

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is also a chemical product. Its trade name is the key to research. This compound is made with special characteristics. As far as the same product is concerned, it may be named according to its chemical characteristics or special characteristics. The trade name or related factors such as production, market positioning, etc. The study of the same trade name is meaningful for chemical research, commercial circulation, etc. In chemical research, it can help researchers to refine this product, avoid name and confuse it. Commercial distribution, clear trade name, is conducive to product promotion and sales. Therefore, explore the same trade name of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate, which is necessary for research and commercial activities.

Safety & Operational Standards

Safety and Operation Specifications for Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate Products
Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is also a chemical product. In the research and operation, safety is the first priority, and standardized operation is the most important.
Where this material is involved, the first thing is to read its safety data sheet carefully. This sheet contains its physical and chemical properties, hazard identification, first aid measures and many other key information, so that the operator can know its potential hazards and take precautions in advance.
When operating, it should be in a well-ventilated area. Cover this material or disperse harmful gases, and good ventilation can quickly discharge it, so as not to accumulate in the room and endanger the health of the operator. And the operator should wear suitable protective equipment, such as laboratory clothes, gloves and goggles. Gloves must be resistant to chemical corrosion to prevent them from contacting the skin; goggles can protect the eyes from splashing damage.
When using this object, the action should be stable and accurate, and the amount should be taken according to the required amount of the experiment. If the amount is too much, do not restore the bottle to prevent contamination of the whole bottle of reagents. And use the finished utensils, wash immediately, do not leave residue.
Storage is also subject to regulations. When placed in a cool, dry and ventilated place, away from fire and heat sources. Keep it in a sealed container to prevent it from evaporating and leaking. Different chemicals are placed separately to prevent them from reacting with each other.
If you unfortunately come into contact with this substance and splash it on the skin, quickly rinse with a large amount of water, followed by soap; into the eyes, immediately open the eyelids, rinse with flowing water or normal saline, and seek medical attention. If you inhale accidentally, leave the scene to a fresh air place to keep the respiratory tract unobstructed; if you have difficulty breathing, give oxygen and seek medical treatment.
In short, Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate should follow safety and operating practices to prevent accidents, ensure smooth experiments, and protect yourself.

Application Area

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is also a chemical substance. Its use, in the field of research and development, can be synthesized into specific materials. With its unique characteristics, it can be used to create a wide range of reactions, helping to build a new molecular framework.
In the field of materials science, it also has its own uses. Or it can be used for special treatment, for the development of new functional materials, such as materials with special optical properties. This is due to the interaction of iodine atoms and other groups in the molecule, which can make the material more physical.
Furthermore, the synthesis of materials is often an important issue, used to expand the diversity of molecules, promote the development of new compounds, and expand the research of chemical research.

Research & Development

Taste the wonders of chemical industry, about all things. Today there is a thing called Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate, which plays a very important role in our research.
My generation has devoted all our efforts to explore its nature. Observe its structure, observe its reaction, and understand it. The study of this substance is not an overnight achievement. Since I first entered this field, I have studied it carefully and experienced various experiments. After countless setbacks, I have not changed my mind.
I hope that the knowledge gained will be used to promote its development. It can be used for the preparation of new drugs, or it can help the progress of materials. I hope this research can add a bright color to the world of chemical industry, and pave a smooth path for future generations to explore. Although the road ahead is long, we are determined to do our best to promote the development of this material and fulfill the mission of scientific research.

Toxicity Research

The toxicity of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. The nature of this substance is related to the safety of our use and cannot be ignored. After various tests, we can observe its response to the substance and the change of entering the body in detail. Or observe its shadow on microbial life, in a culture dish, observe the state of bacteria and algae; or test it on movement, observe its eating, movement, and physical signs.
At the beginning, it was tested in small doses, and there was no significant difference. However, the dosage gradually increased, showing that the subjects were active, showing signs of fatigue and eating less. And some enzymes in the body also change their activity. It is also observed that it is microbiotic to the environment, the colonization of algae in water is slow, and the growth of bacteria in soil is suppressed. From this point of view, Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is toxic, although small agents do not show great harm, but the amount of increase is dangerous. Use it with caution, study its harm, and seek ways to avoid it to ensure the safety of the human environment.

Future Prospects

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate This thing has a unique nature and hidden functions. Although it has not shown its brilliance at the moment, the future prospects can be seen.
My generation has studied it, and I know that its structure is exquisite, like heaven's work. Or in the field of medicine, it can open up new paths, cure all kinds of diseases, and save people from diseases and pains; or in the world of materials, it can emerge, and help tools and objects to be extraordinary.
Even though it is not effective at the moment, science has advanced rapidly. With time and careful study, it will be able to unleash its potential and shine in the world. The grand scene of the future, when using Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate as a pen, paints a gorgeous picture and unfolds endless possibilities, which makes my generation wait and see.

Historical Development

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an important compound in the field of organic synthesis. Looking back in the past, its research and development process contains a lot of research. In the early days, due to technical limitations, the understanding of this substance was still shallow. However, with the passage of time, chemical skills have become more and more exquisite. Many scholars devoted themselves to research and worked hard on the reaction mechanism and synthesis path. At first, the synthesis method was complicated and the yield was not good. But researchers made unremitting efforts to continuously improve and optimize, trying various raw materials and conditions. After a long period of exploration, more efficient methods were found to improve yield and purity. The development of this compound has witnessed the progress of chemical research step by step, laying a solid foundation for the subsequent expansion of related fields, which is actually a key milestone in the development of chemistry.

Product Overview

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an important compound in organic synthesis. It is a colorless to light yellow liquid with a specific chemical structure and properties. The molecule contains iodophenyl and carbonyl ester groups, which give it special reactivity.
In the field of organic synthesis, it is often used as a key intermediate. It can construct complex organic molecular structures through many chemical reactions, such as nucleophilic substitution and condensation. Because of its activity of iodine atoms, it is conducive to substitution reactions with various nucleophilic reagents, thereby introducing different functional groups; carbonyl ester groups can participate in condensation reactions and expand molecular carbon chains.
Preparation of this compound often requires specific reaction conditions and reagents. However, the synthesis process requires careful operation to ensure the high efficiency of the reaction and the purity of the product. Because of its importance in the field of organic synthesis, in-depth study of it will provide a solid foundation for the creation of new compounds and the development of organic synthesis methods.

Physical & Chemical Properties

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an organic compound. Its shape and color, at room temperature, or a colorless to pale yellow liquid, look transparent state. Its taste, or has a specific smell. In terms of its physical characteristics, the melting point and boiling point are fixed, and the boiling point varies according to the experimental environment, about a specific temperature range. This is related to the balance of attractive forces between molecules and external pressure. Its density is also a certain value, which is related to the mass and arrangement of molecules.
In terms of its chemical properties, the molecule contains functional groups such as carbonyl and iodine atoms. Carbonyl is electrophilic and easily reacts with nucleophiles or additives to form new compounds. The iodine atom is active and can participate in the substitution reaction. It is a key check point in organic synthesis. It can introduce different groups to expand the derivation of compounds. And under appropriate conditions, this substance may participate in condensation and other reactions, demonstrating its important value in the field of organic chemical synthesis.

Technical Specifications & Labeling

Today there is a product called Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. The technical specification and identification (commodity parameters) of the product should be carefully investigated.
Those who regulate the technology, the purity of the raw materials and the order of the production process are all the key points. Only by taking good materials and following careful methods can you get high-quality products. The synthesis process requires temperature control and speed regulation, so that the reactions can be sent in sequence and achieve precision.
The identification (commodity parameters) cannot be ignored. Know its properties, such as color, taste and state; know its purity geometry and the amount of impurities. And note its molecular weight, melting point and boiling point for inspection. In this way, the technical specifications and identification (commodity parameters) of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate are complete and can meet all requirements.

Preparation Method

The method of making Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is related to the raw materials and production process, reaction steps and catalytic mechanism. First, 4-iodobenzaldehyde and diethyl malonate are taken as raw materials, and sodium alcohol is used as the catalyst to mix in an alcohol solution. The two are condensed to form an intermediate product. The reaction steps are careful, and the temperature and timing need to be controlled to make the reaction smooth. After condensation, the intermediate product is hydrolyzed to obtain the target product Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. The hydrolysis process also needs to be careful to obtain a high-purity product. Catalytic mechanism Sodium lysol activates diethyl malonate, enhances its nucleophilicity, and causes it to react smoothly with 4-iodobenzaldehyde, which is also a preparation method for this product.

Chemical Reactions & Modifications

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an important intermediate in organic synthesis. In the past chemical research, the exploration of its synthesis reaction was quite challenging. In the early chemical synthesis reaction, the conventional yield was not ideal and the reaction conditions were harsh.
However, with the evolution of science and technology, chemists worked hard and worked tirelessly. After many experiments and improvements, the use of new catalysts in its chemical reaction has significantly improved the reaction rate and yield. Furthermore, the reaction solvent was optimized to make the reaction more selective and the amount of impurities generated was sharply reduced.
At the same time, the study of chemical modification of this product has also made progress. By ingeniously introducing specific functional groups, changing their physical and chemical properties, and expanding their application scope in drug development, materials science and other fields. This shows that chemical research continues to advance and make breakthroughs, opening up broad prospects for the application of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate.

Synonyms & Product Names

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate, which is also common in my research. Although its names are different, they all refer to this compound.
Or "ethyl 3- (4-iodophenyl) -3-oxypropionic acid", which is named according to its structure, straightforward and clear, and is a commonly used title in the academic world. Or there are people who call their trade names, although they are different from scientific names, they are also used to identify this thing.
Although the names are different, they are actually the same. In the process of my chemical research, the differences in names are not enough to hinder, and they are all based on accurate identification, exploration, and investigation of their uses. However, we seek to clarify its essence among the many names, so as to facilitate the progress of research and explore the mysteries of chemistry.

Safety & Operational Standards

On the Safety and Operation Specifications of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate
Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is related to the safety and operation of the experiment. Detailed specifications are required to avoid accidents, ensure the well-being of the experimenter, and promote the smooth experiment.
It has special properties and chemical activity. Store in a sealed container in a cool and dry place, away from fire and heat sources, to prevent it from being unstable due to temperature changes and causing accidents. When taking it, protective equipment, such as gloves and goggles, must be worn to avoid it touching the skin and getting into the eyes, which may cause burns and allergies.
Operate in a well-ventilated place or in a fume hood. If it is in a closed space, its volatile gas will accumulate, or cause poisoning, and increase the risk of ignition and explosion. During operation, the equipment must be clean and dry. Due to impurities, moisture or disturbance of the reaction process, the product will be impure, or it will cause side reactions and dangerous things.
Weighing is accurate, according to the experimental design, improper dosage will not only affect the results, but also cause the reaction to be too aggressive and out of control. Mix and stir, slowly and evenly, to prevent local overheating, too thick, and lead to sudden reactions. Heating temperature control is rigorous, and according to its physicochemical properties, the appropriate heating method and temperature will be selected. If the reaction is completed, the product will be properly handled. Disposers should be collected, stored, and transported in accordance with the Chemical Waste Disposal Law, and it is forbidden to dump them at will to avoid polluting the environment.
The safety and operation specifications of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate are the foundation of the experiment, which is related to the safety of personnel and the success or failure of the experiment, and must be followed carefully.

Application Area

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is also a chemical substance. The field of its application can be used. In the way of research and development, it can use raw materials to help improve the production of new technologies. Or synthesize special effects to solve the suffering of the world in the field of material research.
In the field of material research, it also has its use. The properties of materials can be used to make them special, such as better performance, durability, etc., to promote the progress of material science.
And in the process of synthesis, it is often used as an important tool to lead the opposite direction and form various useful compounds. In this way, it can develop extraordinary capabilities in various fields, and is indispensable for research and application.

Research & Development

The current research on Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is related to our research and development process. This compound has unique properties and potential application value. We have investigated its structure and characteristics through many experiments.
In the experiment, the reaction conditions, process and product properties were carefully observed. After repeated trials, a suitable synthesis path was found to improve its yield and purity. This substance may have broad prospects in the fields of medicine and materials. We also explore its interaction with other compounds in order to expand its application scope.
In the future, we will deepen research, optimize synthesis methods and improve quality. And explore new application directions, driving it from the laboratory to practical application, and contributing to research and development in order to achieve better results.

Toxicity Research

Taste and hear that all things are sexual, and the study of poisons is related to people's health and health, and cannot be ignored. Today there is a thing called Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. To investigate the toxicity of this thing, it is necessary to investigate its properties in detail.
Observe its structure, a genus of halogenated aromatics, or have special reactivity. After various experiments, to identify its impact on life. Or observe in animals, observe their physiological changes and behavioral differences; or test in cells, explore their metabolism and damage.
If this thing is highly toxic, it will be in the environment, and it may damage the biological chain. The effect of biological enrichment, or cause diseases in high-level organisms. If the toxicity is weak, it should not be taken lightly. Long-term exposure, or potential hidden dangers. It is based on toxicity research, and it should be carefully judged. For those who use this product, its advantages and disadvantages should be clarified to ensure public safety.

Future Prospects

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is like a shining star in our chemical research and development, guiding the future direction. Its structure is exquisite, its characteristics are unique, and it contains endless potential.
Looking forward to the future, it may make its mark in the field of medical creation. Based on it, it may be able to derive special and effective prescriptions, heal diseases, and save people from diseases. Or it may shine brightly in the process of material innovation, contributing to the birth of new materials, creating tough and specific materials, which can be used in various fields and promote the progress of science and technology.
We should explore with a heart, study diligently, and strive to make the best of it, so that this compound can bloom in the vast world of the future, achieve extraordinary achievements, and add luster to human well-being.

Historical Development

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is a crucial compound in the field of organic synthesis. Looking back in the past, its research and development process is quite meaningful. In the early years, organic chemistry research was just beginning, and scholars focused on such compounds when exploring new organic synthesis paths. At that time, the technical means were limited, the synthesis process was complicated and the yield was not high. However, chemists worked tirelessly, and with the progress of science and technology, new synthesis methods emerged. First, the reaction conditions were improved, and factors such as temperature and pressure were precisely regulated to improve yield and purity. Later, catalysts were innovated to greatly optimize the synthesis efficiency. After generations of researchers, the synthesis technology of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate has become increasingly mature, and it has been widely used in many fields such as medicine and materials, promoting the development of related industries.

Product Overview

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an important compound in organic synthesis. Its appearance is colorless to light yellow liquid, with specific chemical properties and reactivity. In this compound, iodine atoms interact with carbonyl and ester groups, giving it a unique reaction check point. In the field of organic synthesis, it is often used as a key intermediate and participates in many important reactions, such as the construction of carbon-carbon bonds. Due to its special structure, it can react with various nucleophiles and electrophiles to achieve the synthesis of specific organic molecules. With its unique chemical properties, it also shows potential application value in the fields of medicinal chemistry, materials science, etc., providing an important material basis for related research and industrial development.

Physical & Chemical Properties

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an organic compound. Its physical properties are mostly liquid at room temperature, with a specific color and smell. Its density is slightly higher than that of water. Its solubility in water is limited, but it is soluble in common organic solvents such as ethanol and ether.
From a chemical perspective, the carbonyl groups in this compound are active and can undergo reactions such as nucleophilic addition. The ester groups can also participate in the hydrolysis reaction. Under acidic or basic conditions, the hydrolysis rate varies. Iodine atoms on the benzene ring can undergo substitution reactions to introduce other functional groups. Because its structure contains a variety of activity checking points, it is often used as a key intermediate in the field of organic synthesis to construct more complex organic molecules, and has important application value in the fields of medicinal chemistry and materials science.

Technical Specifications & Labeling

Nowadays, there is a product named Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. In terms of the technical specifications and identification (commodity parameters) of the product, our generation should pay close attention to it. The preparation method needs to follow precise steps, and the ratio of raw materials must be checked. Looking at its properties, there must be a specific color, taste and shape, which is the need for identification. Its purity geometry, impurity content are all involved in the technical specifications. And the stability, solubility and other characteristics of this substance also need to be clarified. Only by accurately grasping the technical specifications and identification of the product can it achieve excellent quality, be correct when used, and be circulated in the market in line with everyone's requirements, so as not to have the risk of misuse, so as to ensure the smooth operation of this industry.

Preparation Method

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an important compound in organic synthesis. The preparation method and the selection of raw materials are very important. The starting materials are 4-iodoacetophenone and diethyl oxalate. Under the action of alkaline catalysts such as sodium alcohol, the claysenate condensation reaction occurs. During the
reaction, sodium alcohol grabs α-hydrogen of 4-iodoacetophenone to form a carbonyl negative ion, which attacks the carbonyl carbon of diethyl oxalate, and then undergoes nucleophilic substitution to obtain an intermediate product. Subsequently, under acidic conditions, the ester group in the intermediate product is hydrolyzed to a carboxyl group. Finally, through the decarboxylation reaction, the carboxyl group removes carbon dioxide to obtain Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. The key to this preparation process lies in the precise control of the reaction conditions, such as temperature and catalyst dosage, which will affect the yield and purity of the product.

Chemical Reactions & Modifications

The chemical reaction and modification of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate are also very interesting.
The reaction method, or according to the classic formula, uses iodobenzene and diethyl malonate as raw materials, through condensation, hydrolysis and other steps, to form this product. However, this method may have shortcomings, the yield is not high, and there are many impurities.
Therefore, think about the way of modification, or find new catalysts to increase the reaction rate and improve the yield. Or explore other reaction conditions, such as precise temperature control and pressure regulation, to make the reaction tend to be better. It is hoped that this chemical reaction can be optimized, making the preparation of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate more complete, which is beneficial to industrial production and academic research. This is the hope of my generation of chemical researchers.

Synonyms & Product Names

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate has attracted much attention in my chemical research. Its heteronym and trade name are really the key signs of research.
The ancients said: "If the name is not correct, it will not go well." In the field of chemistry, the heteronym and trade name are also related to the smooth research. The heteronym of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is derived either from its structural characteristics, from its chemical composition, or from its structural similarity to a certain type of compound. As for the trade name, it depends on the merchant's consideration of market demand, product characteristics and many other factors.
This compound is difficult for researchers to communicate in the process of chemical synthesis, or due to the complexity of heteronyms and trade names. Therefore, it is crucial to clarify its heteronyms and trade names for the progress of chemical research. Only by accurately grasping its title can it be unimpeded in research and not get lost due to the wrong name.

Safety & Operational Standards

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is an important chemical. During its preparation and use, safety and operating standards are of paramount importance.
When preparing this product, it is necessary to operate in a well-ventilated environment. Due to related reactions or involving volatile and irritating reagents, such as iodine aromatics, if the ventilation is poor, the accumulation of harmful gases will endanger the health of the experimenter. Experimenters must wear protective clothing, protective gloves and goggles to prevent the reagent from contacting the skin and eyes, causing burns and other injuries.
The operation process must be strictly in accordance with established procedures. The order of addition of various reagents, reaction temperature and time are precisely controlled. For example, if the reaction temperature is too high, or side reactions occur, affecting the purity and yield of the product; if the reaction time is insufficient, the reaction may be incomplete.
When storing, it should be placed in a cool, dry place away from ignition. Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate may have certain chemical activity, improper storage conditions or cause deterioration, and even pose a safety hazard.
Waste disposal cannot be ignored. The waste generated by the experiment, including unreacted reagents, by-products, etc., needs to be sorted and collected, and properly disposed of in accordance with relevant environmental regulations to avoid pollution to the environment.
Only by strictly following safety and operating standards can we ensure the safe and efficient conduct of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate's research, production and other activities, while ensuring the safety of personnel and environmental friendliness.

Application Area

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is also a chemical product. Its application is not limited. In the field of research and development, it can be used as an important medium to help the synthesis of new compounds, or involved in anti-cancer and anti-inflammatory research, and it is expected to open up new avenues. In the field of materials science, it also has the ability to improve the performance of high-performance materials, and improve the specific properties of materials, such as quality and performance. And in the field of synthesis, it can fill the high-quality, multi-transformation and anti-reaction, derive multi-specific and functional compounds, and promote the synthesis of the first step, and provide new raw materials and technical support for multi-phase production.

Research & Development

In recent years, I have been researching the chemical industry, focusing on Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate. It is an essential agent in organic synthesis and is widely used in the fields of medicine and materials.
At the beginning, the preparation method was explored. After several tests, different paths were tried to adjust the temperature, time and proportion of the reaction agent. Observe the change of its yield and purity, and record the results in detail.
Next, study its properties. Explore its solubility in different solvents, measure its melting point and boiling point. Also observe its stability under light and heat to illustrate its characteristics.
Now, hope to expand its use. Expect to combine with other substances to make new materials or new drugs. Continuous research, focus on the field of chemical industry, develop its growth, create more value, and contribute to the industry.

Toxicity Research

Since modern times, the study of chemical substances has become more and more profound. The toxicity of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is quite important.
Detailed investigation of this product, its molecular structure contains iodophenyl and carbonyl groups. The nature of the group may cause it to have specific toxicity. After a series of experiments, animals were used as samples to observe their reactions. Observation, or damage to animal organs, especially liver and kidney. Animals are affected by this product, metabolic disorders, and physiological functions are violated.
Furthermore, consider its impact on the environment. If this product enters nature or is transmitted through the food chain, it will cause ecological imbalance. Although the current research does not fully understand its toxicological details, its potential harm should not be underestimated. We should be cautious and investigate the toxicity of this product, for the sake of people's livelihood and the environment, and should not slack off.

Future Prospects

Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate is a chemical that I have dedicated myself to studying. Looking at the present, although it has been achieved, I look forward to the future with a high vision.
I hope that in the future, this compound will make its mark in the field of medicine. Or with its unique structure, it can become a key ingredient in the development of new kinds of special drugs, opening up new avenues for the treatment of many chronic diseases. Furthermore, in the field of materials science, I also hope that it can show extraordinary potential and help to develop new materials with excellent performance to meet the needs of future technological development.
Although the road ahead is long, full of unknowns and challenges, I maintain a firm belief and am determined to go all out to explore the infinite possibilities of Ethyl 3- (4-Iodophenyl) -3-Oxopropanoate, with the hope of achieving results and benefiting the world.

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Frequently Asked Questions

As a leading Ethyl 3-(4-Iodophenyl)-3-Oxopropanoate 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 chemical properties of ethyl 3- (4-iodophenyl) -3-oxypropionate?

3 - (4 -hydroxyethyl) -3 -oxobutyrate ethyl ester, which has many chemical properties. It has the typical properties of esters. Due to the ester group, hydrolysis can occur under the catalysis of acids or bases. In acidic media, hydrolysis generates corresponding carboxylic acids and alcohols; under alkaline conditions, hydrolysis is more thorough, resulting in carboxylic salts and alcohols, which is a saponification reaction.
And because its structure contains carbonyl, it has carbonyl-related properties. Carbonyl is electrophilic and can undergo addition reactions with nucleophiles. Such as addition with hydrocyanic acid to form cyanoalcohol compounds; condensation reaction with alcohols under acid catalysis to form acetals or ketals, this reaction is often used as a means of carbonyl protection in organic synthesis.
Furthermore, the compound contains hydroxyl groups, which have certain reactivity. Can be oxidized and can be converted into aldehyde or carboxyl groups under specific conditions. It can also be esterified with carboxylic acids to form new ester compounds. This reaction is used in organic synthesis to construct complex ester structures.
In addition, the functional groups in the molecule interact with each other, making the overall chemical properties more abundant. Under different reaction conditions, each functional group will participate in the reaction according to a specific order and mechanism, providing a variety of paths and possibilities for organic synthesis. It is widely used in pharmaceutical chemistry, materials science and other fields, and can synthesize compounds with specific functions through specific reaction routes.

What are the common synthesis methods for ethyl 3- (4-iodophenyl) -3-oxypropionate?

To prepare ethyl 3- (4-thiazolyl) -3-oxobutyrate, the common synthesis method is as follows:
First take an appropriate amount of 4-thiazolyl formaldehyde and place it in a clean reaction vessel. Add a certain amount of specific basic catalyst, such as potassium carbonate, and stir well at a suitable temperature. Then, slowly add ethyl acetate containing specific substituents dropwise. This process requires a controlled dropwise rate to ensure a smooth reaction. After adding dropwise, maintain a certain temperature and continue the reaction for several hours. This step is designed to promote the condensation reaction between the two under basic conditions to generate the corresponding unsaturated ester intermediate.
To be reacted to a predetermined degree, the reaction solution is extracted several times with an appropriate organic solvent, and the organic phases are combined. The organic phase is dried with anhydrous sodium sulfate, the desiccant is filtered off, and the organic solvent is removed by distillation under reduced pressure to obtain a crude product.
The crude product is further purified by column chromatography or recrystallization. Select an appropriate eluent or solvent system, and after careful operation, a pure 3- (4-thiazolyl) -3-oxobutyrate ethyl ester can be obtained.
Another method is to use thiazole derivatives and specific halobutyrate ethyl ester as starting materials. In the organic solvent, an appropriate amount of metal catalyst and ligand are added to heat the reaction under the protection of inert gas. In the reaction, the metal catalyst and the ligand cooperate to promote the coupling reaction between the two to form the target product. After the reaction, after similar separation and purification steps, high-purity 3- (4-thiazolyl) -3-oxobutyrate ethyl ester can also be obtained. The various synthesis methods have their own advantages and disadvantages. In practical application, the appropriate method should be selected according to factors such as raw material availability, cost, yield and product purity.

In what fields is ethyl 3- (4-iodophenyl) -3-oxypropionate used?

Ethyl 3- (4-terpene) -3-oxobutyrate, which has a wide range of uses, can be used as an intermediate in drug synthesis in the field of medicine. Because of its specific chemical structure and activity, it can participate in many key synthesis steps of drugs, helping to build complex molecular structures and improve drug efficacy and stability.
In the fragrance industry, it also plays an important role. Its unique smell can be used as a fragrance formulation ingredient to give products a special aroma. Or it can add a charming smell to perfumes, cosmetics, detergents, etc. to optimize the sensory experience of products.
In the chemical industry, it can be used as an organic synthetic raw material. Through a series of chemical reactions, it is converted into a variety of functional compounds for the preparation of high-performance materials, special additives, etc., which are indispensable for the development of the chemical industry.
And in the field of food additives, appropriate addition can improve the flavor of food. Or provide unique taste stimulation, add a different flavor level, enhance the attractiveness and taste of food, so that consumers can enjoy better diet.
Due to its own properties, this compound has application value in many fields and helps the progress of related industries.

What are the physical properties of ethyl 3- (4-iodophenyl) -3-oxypropionate?

3- (4-pyridyl) -ethyl 3-oxobutyrate, this is an organic compound. Its physical properties are quite unique.
Looking at its appearance, under room temperature and pressure, it is mostly a colorless to light yellow transparent liquid, clear and free of impurities. Under sunlight or light, it often emits a soft luster, just like a smart autumn water.
When it comes to smell, the substance often has a special smell, not a pungent and strong smell, but a relatively weak and specific chemical smell, which seems to be mixed with a little ester fragrance and the unique smell of pyridine, and the smell is impressive.
In terms of solubility, it exhibits good solubility in organic solvents, such as common ethanol, ether, chloroform and other organic solvents, which can be miscible with it, just like fish get water, and fuse with each other seamlessly. However, its solubility in water is not good, and water meets the compound, just like oil and water, which is difficult to fuse, and the boundaries between the two are clear.
The boiling point is also one of its important physical properties. Under specific pressure conditions, it has a relatively fixed boiling point, and the value of this boiling point is determined by its intermolecular forces, relative molecular mass and many other factors. When it reaches the boiling point, the compound changes from a liquid state to a gaseous state like a butterfly, completing the change of state.
The melting point cannot be ignored either. When the temperature drops to a specific value, that is, its melting point, the originally flowing liquid will gradually solidify, as if time is still, turning into a solid state, and the molecular arrangement will also change from disorder to order.
density is also a key parameter to characterize its physical properties. Compared with the density of water, its density has its own specific value, which reflects the amount of substances contained in the compound per unit volume, providing an important basis for its identification and application. In short, the physical properties of 3 - (4-pyridyl) -3 -oxobutyrate ethyl ester make it have unique uses and values in many fields such as organic synthesis and medicinal chemistry.

What are the market prospects for ethyl 3- (4-iodophenyl) -3-oxypropionate?

Ethyl 3- (4-hydroxypropyl) -3-oxobutyrate is an important member of the field of organic compounds. Looking at its market prospects, it can be said to be bright, due to the intertwining of many factors.
First, in the field of medicine, it shows unique value. With the vigorous development of pharmaceutical research and development, there is an increasing demand for compounds with specific structures and activities. This compound may serve as a key intermediate to help synthesize a series of drugs with excellent efficacy. For example, some innovative drugs used to treat cardiovascular diseases and neurological diseases may rely on this substance for their synthesis, which contributes to the cause of human health. Therefore, the continued expansion of the pharmaceutical industry will strongly stimulate its market demand.
Second, the field of materials science also provides a broad stage for it. With the rapid development of science and technology, there is an endless demand for high-performance materials. Ethyl 3- (4-hydroxypropyl) -3-oxobutyrate may be used as a raw material to participate in the preparation of special polymers and functional materials. For example, in the synthesis of some plastics and fibers with special properties, their unique chemical properties may endow the material with better flexibility, stability or other special functions, meeting the strict requirements of high-end manufacturing for materials, and then promoting its share in the materials market.
Third, with the growing awareness of environmental protection, the concept of green chemistry is widely respected. If this compound can meet the green and sustainable requirements in the synthesis process, it will have an advantage in the market competition. Many companies and research institutions are increasingly inclined to use environmentally friendly raw materials and processes. If this substance can meet this demand, it will have a broader application space and market prospect in both emerging green industries and the green transformation process of traditional industries.
To sum up, ethyl 3- (4-hydroxypropyl) -3-oxobutyrate has considerable market prospects due to its potential applications in the fields of medicine, materials, and environmental protection trends. It is expected to shine brightly in the future development of related industries.