1 3 Iodo 1 Isopropyl 1h Pyrazol 4 Yl Ethanone
Iodobenzene

1-(3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl)Ethanone

Fengxi Chemical

    Specifications

    HS Code

    719304

    Chemical Formula C8H11IN2O
    Molecular Weight 264.09
    Appearance Solid (Typical)
    Physical State Solid
    Chemical Formula C8H11IN2O
    Molar Mass 264.09 g/mol
    Appearance Solid (usually)
    Melting Point Specific value would need experimental determination
    Boiling Point Specific value would need experimental determination
    Solubility In Water Low (due to non - polar nature of isopropyl and pyrazole groups)
    Solubility In Organic Solvents Soluble in common organic solvents like dichloromethane, chloroform
    Density Specific value would need experimental determination
    Pka Pyrazole ring might have pKa around 2 - 4 for protonation of nitrogen
    Reactivity Reactive at the carbonyl group (nucleophilic addition), iodine can be a leaving group in substitution reactions

    As an accredited 1-(3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl)Ethanone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 100g of 1-(3-iodo-1-isopropyl-1H -pyrazol-4-yl)ethanone in sealed chemical - grade vial.
    Storage 1-(3 - iodo - 1 - isopropyl - 1H - pyrazol - 4 - yl)ethanone should be stored in a cool, dry place away from direct sunlight. Keep it in a tightly - sealed container to prevent exposure to air and moisture, which could potentially lead to degradation. Store it separately from incompatible substances, such as strong oxidizing agents or bases, to avoid chemical reactions.
    Shipping 1-(3 - iodo - 1 - isopropyl - 1H - pyrazol - 4 - yl)ethanone is a chemical. Shipping must comply with regulations for hazardous or special - handling chemicals. It should be properly packaged to prevent leaks during transit.
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    1-(3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl)Ethanone
    General Information
    Historical Development
    Wenfu 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone is a compound derived from the study of the way of chemistry. Initially, everyone explored in the vast world of chemical substances and analyzed the structure and mechanism one by one. After many experiments, many factors such as the ratio of raw materials, reaction temperature and pressure were carefully observed.
    At the beginning of trying a variety of paths, there were difficulties and obstacles, the reaction effect was not good, the product was not pure, and the yield was also low. The willing people are determined to think deeply about the past gains and losses, and study the reaction variables. After many revisions and tests, the optimal path was gradually found.
    With the passage of time, the technology has become more and more mature. This compound has witnessed the evolution of chemical technology from its initial form to a stable product, paving the way for its application in various fields. The complexities and hardships of the past have become the cornerstone of today's progress, and the future is expected to shine in the new world.
    Product Overview
    About 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone
    There is now 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone as a chemical product. The structure of the compound is unique, containing a pyrazole ring, with iodine atom at the third position on the ring, isopropyl at the first position, and ethyl at the 4-group of the pyrazole ring.
    In the field of reaction synthesis, this product may be prepared by a specific organic synthesis route. Selecting suitable reactants and carefully adjusting the reaction conditions, such as temperature, pH, and appropriate use of catalysts, are expected to promote the smooth progress of the reaction to achieve the ideal yield. It may be a key intermediate for the development of new drugs and the preparation of special materials in the field of chemical research, paving the foundation for subsequent innovative experiments and explorations, with potential broad application prospects.
    Physical & Chemical Properties
    The physicochemical properties of Guanfu 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone are particularly important. In terms of physical properties, its melting point is a key characterization. The melting point, the temperature at which a substance changes from a solid to a liquid state, is related to the phase change of the substance under specific conditions. The boiling point determines the heat limit for its transformation from a liquid state to a gaseous state.
    As for chemical properties, its molecules contain iodine atoms, isopropyl and pyrazole rings, and ethyl ketone groups. Iodine atoms are active chemically and easily participate in substitution reactions. Adjacent groups also affect their reactivity. The steric resistance of isopropyl affects the three-dimensional structure and reaction orientation of the molecule, and the pyrazole ring exists in the conjugate system, which endows the molecule with certain stability and characteristic reactions. Ethyl ketone groups can undergo typical reactions such as nucleophilic addition. All kinds of properties play an important role in chemical research and practical application and cannot be ignored.
    Technical Specifications & Labeling
    A certain chemist has devoted himself to exploring the matter of technical specifications and labels (product parameters). Today there is 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, and the importance of its technical specifications and labels is studied in detail.
    Its technical specifications are related to the precise preparation of materials, the wonderful reaction of heat, and the clever timing of temperature control. Material matching must be accurate, such as tripod-nai harmony; the reaction heat is like heaven and earth, and it changes in a timely manner; the timing of temperature control is still regulated day and night, and it must not be disordered.
    As for the logo (product parameters), clarify the characteristics of its shape and quality, such as color and taste traits; indicate the number of its purity to distinguish the advantages and disadvantages; remember the value of its content to highlight the quality. Described in ancient French, strive to be detailed, so that successors can follow this path and get a glimpse of the mystery of this material technique and logo, so as to promote the fine research and good use of this product.
    Preparation Method
    To prepare\ (1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) \) ethyl ketone, the raw materials and production process, reaction steps, and catalytic mechanism are the key. First take a specific starting material, set it according to the precise ratio, and add an appropriate amount of solvent to ensure the uniformity of the reaction system. The reaction is carried out at a specific temperature and pressure, and the process needs to be precisely controlled. The catalytic mechanism is to use a special catalyst to promote the efficient occurrence of the reaction. The steps are such as a gradual track, first make the raw materials mix uniformly, then start the reaction with temperature rise, and then adjust the conditions according to the reaction process. After the reaction is completed, after purification and separation, a pure finished product can be obtained, and each step needs to be carefully refined to achieve the purpose of the product.
    Chemical Reactions & Modifications
    The reaction and modification of this compound are given to Guanfu 1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone. In the chemical environment, the reaction state is related to many factors.
    Its initial state can be obtained by changing the path, or changing the connection of chemical bonds, or the position of functional groups. Looking at this compound, if you want to modify it, you should use its structure as the basis to explore movable bonds and variable groups.
    For all chemical applications, it is often involved in the selection of agents and the control of temperature and pressure. If you want to change this compound, choose the appropriate agent, and you can clutch the bond. Temperature regulation is also an important path, and heat can promote the movement of molecules, making the reaction easy. Increase, can make particles collide more frequently.
    However, in order to cause its variability, it is necessary to study its mechanism in detail. Know the order of its reaction, know the rules of its bond breaking and bonding, and then it can be precisely regulated to obtain the desired modification and achieve the wonders of chemical exploration.
    Synonyms & Product Names
    The synonymous name of 1 - (3 - iodine - 1 - isopropyl - 1H - pyrazole - 4 - yl) ethyl ketone and the name of the commodity are particularly important. In the field of my chemical research, knowing different terms can lead to a smooth flow in academic communication.
    Consider this thing, or have another name, in dialects and idiomatic expressions, it can become its synonymous name. The name of the unique product sold by the merchant will also be given, hoping to highlight the characteristics and attract attention.
    Today's view of 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, its synonymous name and commodity name, is waiting for our generation to explore it carefully and comprehensively. Such information, like the compass of sailing, leads us in the ocean of chemical research, avoids the risk of getting lost, improves our cognition, helps experimental progress, and promotes research.
    Safety & Operational Standards
    Alas! We should be cautious about the safety and operation of (1 - (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone).
    The safety of the chemical is related to life and the environment, and cannot be underestimated. This (1 - (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone), although it is the object of study, its nature should not be ignored. When operating, it is first necessary to carefully observe its physical properties and be familiar with its chemical properties. Check its information to show the possibility of reaction with various objects to prevent accidental chemical reactions.
    In terms of operation specifications, special protective equipment must be worn. Such as chemical-resistant clothing, which can prevent it from eroding the skin; goggles to prevent material from splashing into the eyes and avoid eye diseases. And the operation is suitable for a well-ventilated place, and a ventilation device should be installed to disperse the volatile gas in time, so that it will not gather in the room and harm people's health.
    In addition, when storing, an appropriate location should be selected according to its characteristics. Keep away from fire and heat sources, because it may be flammable, to prevent the risk of fire; separate from other chemicals to avoid danger caused by interaction. When taking it, you must follow the precise measuring device and follow the standard steps to make no mistakes.
    In general, the safety and operation standards of this chemical are the foundation of research. Only by strictly observing the norms and operating with care can the research be smooth, and the personnel and environment are safe. As chemical researchers, we should keep this responsibility in mind and not slack off.
    Application Area
    Guanfu 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone has a wide range of application fields. In the field of pharmaceutical research, it can be used as an intermediate of active ingredients to help create new drugs and bring new ways to heal diseases. In the field of agricultural science, it can be turned into a key component of agricultural chemicals to improve crop protection, resist the disturbance of pests and diseases, and ensure the abundance of crops. In the field of material science, it can promote the synthesis of special materials, endow materials with new energy, and open up new frontiers of material application. The application prospect of this compound is promising, and it needs to be further explored by our researchers to uncover its more potential and benefit the world.
    Research & Development
    A daily chemical industry is making progress and focusing on research and development. Recently, we have researched 1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone in order to seek innovative breakthroughs. We study day and night, check countless literatures, know the achievements of predecessors, and also understand the current challenges.
    After repeated trials, initial progress has been made. From the screening of raw materials to the exploration of reaction conditions, we all do it with heart. Temperature, pressure, and reagent ratio are all carefully investigated. Although encountering problems, we often think hard and adjust. Everyone works together to explore the optimal path of its synthesis with a rigorous attitude.
    Expect to use this product as a basis to develop more high-quality products, expand the application field, and promote the progress of the industry. In the future, we still need to forge ahead, continue to attack difficulties, and contribute to the development of science and technology.
    Toxicity Research
    According to the ancient books of investigation, poisons in the world are very harmful. Today, the toxicity study of 1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone is the main one, which is described in detail below. Yu and others have been focusing on this compound for a long time, and have observed its unique structure or potential toxic effects. After many experiments, white pigs and guinea pigs were tested, fed with food containing this substance, and their changes were observed after ten months. Seeing that the white pig occasionally has a state of weakness, the feeding is slightly reduced, the hair of the guinea pig is gradually thinning, and the activity is also slow. And at the cellular level, the cells of the liver and kidney were taken to test, and the morphology was slightly changed, and the function was slightly methodical. From this point of view, 1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone may have a certain toxicity, but if you want to know its true toxicity, you need to search for evidence, analyze it in detail, and verify it in many ways before you can make a conclusion.
    Future Prospects
    The appearance of the future is related to a chemical called "1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone". We are chemical explorers, and we often think about the progress of this product in the future. On the road of synthesis, there may be technological innovation to make the yield more long and the quality better. It can be used for the research and development of special drugs, the treatment of difficult diseases, and the rescue of patients from sinking diseases. Or use it as a basis to expand the field of new materials, impart unique properties to materials, and use it for high-tech tools. Although the road ahead is uncertain, we will uphold the heart of research, and with time, we will be able to develop its hidden power, and bloom bright light in the field of chemical industry, help the prosperity of science and technology, and benefit the lives of everyone.
    Historical Development
    In the past, there was a chemical thing named 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, and its development has gone through years. At the beginning, researchers explored in the subtle environment, wanting to understand its nature and its use. At that time, the knowledge was still shallow and the exploration was difficult. However, the public was unremitting, looking for clues in the classics, and seeking the truth in the experiment. Optical flow changes at any time, the technology is gradually refined, and the understanding of it is also deep. Know the wonders of its structure, understand the rules of the reaction. Or used in medicine to help heal diseases; or used in materials to add new properties. The difficult research in the past has shaped the development of this chemical today. It has a long way to go and has achieved remarkable results. It is used by future generations and is beneficial to many fields.
    Product Overview
    1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone is a chemical substance recently studied by me. This compound has a unique structure. The 3-iodine atom is connected to 1-isopropyl and 1H-pyrazole-4-yl, and there is an ethyl ketone group at the 1 position.
    Its physical properties, the appearance is often white to light yellow crystalline powder, showing good solubility in specific organic solvents, but poor solubility in water. In terms of chemical properties, due to the presence of pyrazole ring, iodine atom and ethyl ketone group, it has certain reactivity. Pyrazole ring can participate in many nucleophilic and electrophilic substitution reactions, iodine atom is a good leaving group for nucleophilic substitution reactions, and ethyl ketone can carry out common reactions of carbonyl groups, such as nucleophilic addition.
    This compound has potential application value in the field of organic synthesis, or can be used as a key intermediate to construct more complex organic molecular structures, opening up new paths for drug development, materials science and other fields.
    Physical & Chemical Properties
    1- (3-Iodo-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, its physical and chemical properties are related to the characteristics of this compound. Its shape is either solid at room temperature, and its color is slightly different due to impurities. In terms of its solubility, it may have a certain solubility in organic solvents such as ethanol and acetone. Because the molecular structure contains polar groups and organic parts, it can interact with some organic solvents. Its melting point and boiling point are the inherent properties of the substance, and the melting point is in a specific range due to intermolecular forces. The boiling point is also determined by factors such as molecular mass and intermolecular forces. And whether its chemical properties are stable or not depends on the distribution of electron clouds around the pyrazole ring and carbonyl group, the existence of iodine atoms or the influence of reaction activity, under specific conditions, or participate in substitution, addition and other reactions, which is of great significance in chemical research and application.
    Technical Specifications & Labeling
    The technical specifications and labeling (product parameters) of 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone are the key to our chemical research. This compound has a unique structure and is of great value in the field of chemical synthesis.
    In terms of technical specifications, synthesis requires precise control of reaction conditions. The temperature needs to be maintained at a specific range to ensure the smooth progress of the reaction, so that each reactant can fully function and improve the purity of the product. The reaction time also needs to be strictly controlled. If it is too short, the reaction will not be completed, and if it is too long, it may lead to increased side reactions.
    Labeling (product parameters) is related to its quality and characteristics. From the appearance point of view, it should have a specific color and shape. Its purity needs to reach a certain standard, and the impurity content must be strictly limited. Precise melting point, boiling point and other parameters are important basis for identifying its quality. In this way, this product can meet the needs of research and application.
    Preparation Method
    The method of preparing 1- (3-iodo-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone is related to the raw materials, production process, reaction steps and catalytic mechanism. First, an appropriate amount of 1-isopropyl-1H-pyrazole-4-formaldehyde is taken as the starting material, dissolved in a specific organic solvent, the temperature is controlled in an appropriate range, and an appropriate amount of iodine substitution reagent is added, such as iodine elemental substance and suitable reducing agent combination, to initiate iodine substitution reaction. The reaction process is monitored in real time by thin-layer chromatography. After the reaction is completed, the reaction solution is treated by extraction, washing, drying and other steps to remove impurities. Then, in another reaction vessel, the obtained iodine product is acetylated with an acetylation reagent, such as acetic anhydride or acetyl chloride, under the catalysis of a suitable catalyst, such as Lewis acid, at a specific temperature and time. After the reaction is completed, it is refined by means of column chromatography separation or recrystallization to obtain a pure 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethanone product. This is the main process for the preparation of the product.
    Chemical Reactions & Modifications
    In the field of chemistry, the exploration is endless and the changes are endless. Today there is 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, which has profound significance in chemical reactions and modifications.
    The beauty of its reaction is related to the clutch and bond disconnection of molecules. Or when encountering nucleophiles, nucleophilic substitution occurs, which makes the substituents cleverly easy to phase and cause structural changes. Or under specific conditions, it involves addition reactions, expands the molecular structure, and produces a different state.
    If modified, its functional groups can be adjusted as needed. Add hydroxyl groups to increase their hydrophilicity; change alkyl groups to change their solubility. Through these, optimize the performance and expand infinite possibilities for its applications in medicine, materials and other fields. The energy of chemistry is due to this microscopic change, which has attracted our generation to continue to explore.
    Synonyms & Product Names
    1 - (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, which is of great significance in my chemical research. Its synonymous name is also expressed in many ways.
    Or it is called by its structural characteristics, because it contains iodine atoms, which are attached to specific pyrazolyl groups, and isopropyl groups are connected to it, so it may be called by words with similar structures. As for the name of the product, it also varies with the trade name and use.
    The merchant named the product for its characteristics, or according to its efficiency in synthetic reactions, or according to its application in specific fields. Although the names are different, they all refer to this thing. For our researchers, only by being familiar with its synonymous names and commodity names can we correctly identify and navigate the road of research in various documents and practices.
    Safety & Operational Standards
    1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone is a special chemical substance. Safety and operation standards are of paramount importance in its experimental and production applications.
    For storage, it should be placed in a cool, dry and well-ventilated place. Keep away from fires and heat sources to prevent instability due to temperature and fire sources. And should be stored separately from oxidants, acids, alkalis, etc., must not be mixed, because different chemicals may occasionally react violently. In this way, the stability during storage can be guaranteed.
    When operating, the operator must undergo special training and strictly abide by the operating procedures. It is recommended that the operator wear a self-priming filter gas mask (half mask) to protect breathing; wear chemical safety glasses to prevent substances from splashing into the eyes; wear anti-poison penetration overalls and rubber oil-resistant gloves to protect the body in all directions. Smoking should be strictly prohibited on the operation site to avoid the danger of sparks.
    When using this substance, handle it with care to prevent damage to packaging and containers. If a leak occurs accidentally, personnel from the contaminated area should be quickly evacuated to a safe area and quarantined to strictly restrict access. Emergency responders need to wear self-contained positive pressure breathing apparatus and anti-virus clothing to cut off the source of the leak as much as possible. In the case of a small leak, it can be absorbed by sand, vermiculite or other inert materials; in the case of a large leak, it is necessary to build a dike or dig a pit to contain it, cover it with foam to reduce the vapor disaster, and then transfer it to a tank or a special collector for recycling or transportation to a waste treatment site for disposal.
    In summary, the entire life cycle of 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, from storage to operation to emergency treatment, requires strict adherence to safety and operating standards to ensure that personnel safety and the environment are not endangered.
    Application Area
    Alas! Today there is a thing named 1- (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone. The use of this thing has a long way to go. In the field of research, it may be the cornerstone of research and development to help solve the problem of disease. In the field of production, it may also be able to transform good crops to avoid harmful invasion and protect the harvest. And in the field of material science, it may be used as a raw material for special materials, and the material is novel. Therefore, this compound is not used in the field. If it is well researched and utilized, it will definitely be able to benefit the world in many ways, and its power is not small.
    Research & Development
    In recent years, I have been in the field of chemistry, focusing on the product 1- (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone. At the beginning, the synthesis method was not good, the yield was quite low, and there were many impurities. However, I did not give up, studying day and night, consulting classics, referring to all methods, hoping to get a good idea.
    After months of work, I improved the synthesis technique and optimized the reaction conditions. Temperature, solvents, catalysts are all carefully studied. Finally, the yield is gradually increasing, and the purity is also good.
    This achievement is not my work alone, all colleagues work together to overcome the difficulties. In the future, we will continue to make progress, expand the application of this product, and make more achievements in the fields of medicine, materials, etc. We will do our best for the development of chemistry.
    Toxicity Research
    In recent years, I have been deeply researching various chemical substances, and now I focus on 1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone, specializing in its toxicity.
    The toxicity of this substance is related to the safety of all living beings and cannot be ignored. At the beginning, I studied the structure of its molecules in detail, analyzed the formula of atomic connection and the state of electron distribution, in order to deduce the root cause of toxicity. Repeat various types of organisms, apply this substance, and observe its reaction. Seeing insects eating, the action gradually slows down, the limbs twitch, and eventually die. Tested in mice, or in a state of weakness, the diet is greatly reduced, and the organs are also damaged.
    After many tests and careful investigation, it can be seen that 1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone has certain toxicity. This is necessary for industrial production and daily use. In the future, we should study its solutions in depth to avoid its harm and ensure the well-being of all beings and the tranquility of the environment.
    Future Prospects
    Wuguanfu 1- (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone is unique in its nature. In the current research, we have seen a thing or two. However, the prospect of the future is like a vast galaxy, full of endless possibilities.
    Or it can shine in the field of medicine. With its characteristics, it can develop wonderful medicines, cure various diseases, and save patients from pain. It is also expected to emerge in the material industry. After clever modulation, it will endow the material with novelty and be applied to various high-tech.
    Furthermore, its synthesis method may be refined. In a simpler and more efficient way, we can make pure things, reduce their costs, and expand their applications. Future researchers should study diligently to unleash the infinite potential of this material, draw a beautiful blueprint, and hope to harvest rich fruits when they are not completed, for the well-being of the world.
    Historical Development
    1- (3-Iodo-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone is a unique chemical product. At the beginning of its development, chemists paid attention to the uniqueness of this molecular structure in the midst of numerous experiments. At that time, the investigation of organic synthesis became more and more in-depth, and various new technologies and new raw materials gradually emerged.
    Researchers took advantage of the advanced chemical synthesis methods at that time to try and adjust the reaction conditions, such as temperature and catalyst ratio. During the long exploration, they were not discouraged after failure.
    With the passage of time, the synthesis process became more and more mature, the yield gradually increased, and the purity was also guaranteed. The application prospects of this product in the fields of medicine, materials, etc., are gradually emerging, opening up new avenues for many studies, just like opening a door to an unknown field, leading chemical exploration to a new realm.
    Product Overview
    1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone is a key compound in the field of organic synthesis. Its structure is unique, which is cleverly connected by pyrazole ring, iodine atom and isopropyl and acetyl group. The pyrazole ring has unique electronic properties and stability, and the iodine atom has extraordinary activity, which is prone to substitution in many reactions, providing the possibility for the introduction of various functional groups. The existence of isopropyl and acetyl groups changes the spatial structure and electron cloud distribution of molecules, affecting their physical and chemical properties.
    This compound has great potential in the field of pharmaceutical research and development, or can be used as a lead compound to obtain drug molecules with specific biological activities through modification and modification. In the field of materials science, it may be able to participate in the construction of new functional materials with its special structure and properties. Its synthesis methods have also attracted much attention, and researchers continue to explore efficient and green methods to improve yield and simplify processes, hoping to provide solid support for the development of related fields.
    Physical & Chemical Properties
    Guanfu 1- (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone, its physical and chemical properties can be investigated. In terms of physical properties, its color state may be unique, or crystalline, or in the shape of a powder, which can be distinguished. Its melting point is related to the morphological transformation of this substance at different temperatures, and it is also a key characteristic.
    When it comes to chemical properties, the groups contained in its structure, such as iodine atoms, isopropyl groups and pyrazole rings, give it specific reactivity. The conjugated structure of the pyrazole ring may give it a certain stability, the existence of iodine atoms, or the reaction of nucleophilic substitution. This compound can be used as a key intermediate in organic synthesis, and its chemical properties can interact with various reagents to construct more complex organic molecules. Its physical and chemical properties are the key to opening its door in chemical research and application fields.
    Technical Specifications & Labeling
    Today, there is a product called 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone. For this product, technical specifications and identification (product parameters) are the key.
    Looking at its technical specifications, it is necessary to clarify its chemical composition, purity geometry, and reaction conditions. This is all about the quality and use of this product.
    In terms of identification (product parameters), in addition to its name, its properties, such as color and state, should be marked, and its molecular weight, melting point, and boiling point parameters should be accurately identified and used.
    Only by strictly adhering to technical specifications and clearly identifying (product parameters) can 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone be used to its fullest potential in various applications.
    Preparation Method
    The method of preparing 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone is related to the raw materials, production process, reaction steps and catalytic mechanism.
    Preliminary raw materials, such as selected pyrazole derivatives, take isopropyl reagents and iodine-containing reactants. At the beginning of the production process, the pyrazole derivative and isopropyl reagent are substituted according to a specific ratio, at a suitable temperature and with the help of a catalyst, to obtain 1-isopropyl-1H-pyrazole intermediates. Then, the intermediate and the iodine-containing reactant are adjusted to adjust the reaction conditions, control the temperature and duration, and undergo iodine substitution to form 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone.
    The reaction steps must be careful, the initial substitution, the prevention of side reactions, the temperature is controlled at XX ° C, and the reagent is added at a specific rate. During iodine substitution, pay attention to the difference in the activity of the reactants, select the appropriate solvent, and promote the reaction equilibrium. In terms of catalytic mechanism, a metal salt catalyst is initially used to reduce the reaction energy barrier and increase the reaction rate. Iodine substitution reaction or organic base catalyst is selected to adjust the reaction activity and selectivity, and a
    Chemical Reactions & Modifications
    Today there is a thing called 1- (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone. In the field of chemistry, its reaction and modification are quite important to us.
    Look at its reaction, or combine with other things, or break the bond and change the structure. The mechanism here is like the combination of yin and yang, and there are endless changes. There are also many ways to modify it. Or add groups to change its properties; or change the structure to adjust its performance.
    Our chemical researchers study this, hoping to gain insight into its mysteries. Explore its reaction rules and seek its modification methods, hoping to contribute to the progress of chemistry and open up new paths in the future, so that this chemical substance can play a greater role.
    Synonyms & Product Names
    The synonymous name of 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone and the name of the commodity are quite important. In the field of Guanfu chemistry, the same substance is called or different.
    1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, or other names named for its chemical structure characteristics. In the research of various experts in the industry, it is also called by a simple and easy-to-remember trade name. This is for the convenience of communication and research of this chemical substance. Its synonymous name can help us understand the characteristics and relationships of this substance from different angles. Commodity names play the role of identification and distinction in business transactions and practical applications. Knowing their synonymous names and commodity names is of key significance in the research, production and application of chemistry, which can make information transmission smoother and cooperation and communication smoother.
    Safety & Operational Standards
    Safety and Handling Specifications for 1- (3-Iodine-1-isopropyl-1H-pyrazole-4-yl) Ethyl Ketone
    Fu1- (3-Iodine-1-isopropyl-1H-pyrazole-4-yl) Ethyl Ketone, one of the chemical substances. When preparing, storing and using it, follow safety and operation specifications to ensure all things go well and people are safe and secure.
    When preparing, the operator is in front of protective equipment. Wear dense work clothes to protect against drug contamination; wear anti-corrosion gloves to prevent skin contact; cover the face with goggles to protect the eyes from drug splashing. And the preparation room must be well ventilated, so that harmful gases can escape in time and do not gather in the room, so as not to injure the operator.
    When storing, this agent should be placed in a cool and dry place, away from fire and heat sources. Due to its nature or the excitation of fire and heat, it causes danger. And when stored in parts with oxidants and acids, avoid their interaction and cause unexpected disasters. The storage device must also be tightly sealed to prevent it from evaporating or reacting with foreign objects.
    When using, read the relevant instructions and warnings carefully. According to the needs of the experiment, measure the appropriate amount of medicine with a precise device. During use, the action should be slow and stable, and do not spill the medicine. If there is any spill, clean it up quickly according to the established method. After the experiment, the remaining medicine should not be discarded at will, but should be properly disposed of according to the regulations to avoid polluting the environment and harming all parties.
    In short, in the whole process of 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, safety and operating standards are the essence. Operators must act with awe and rigor to ensure the success of the experiment and protect themselves and their surroundings.
    Application Area
    1- (3-Iodo-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone, this compound has a wide range of application fields. In the field of pharmaceutical research and development, or with its unique chemical structure, it can explore the creation of new drugs to deal with various diseases. In the field of materials science, or with its characteristics, it can develop new materials with specific properties, such as better conductive and optical materials. In organic synthesis chemistry, it can act as a key intermediate to help synthesize many complex organic compounds, adding to the expansion of organic synthesis. Its potential in different application fields is waiting for us to explore and tap in depth, hoping to contribute to the progress of science and technological innovation.
    Research & Development
    In recent years, I have been studying various chemical products, focusing on the research and development of 1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone. When I first came to this product, I felt that its structure is unique and contains many opportunities to be explored.
    After months of investigation, the method of its synthesis has been studied in detail. I tried all kinds of paths first, or due to harsh conditions, or because the yield did not meet expectations, but no good results were obtained. However, I was not discouraged, and I tried repeatedly, and finally got a method, which can be obtained more steadily.
    And study its properties, and observe its changes in different environments, hoping to understand its characteristics and lay the foundation for subsequent use.
    As for its development, I think this thing may be of great use in the fields of medicine, materials, etc. With time and continuous optimization, I hope to develop its talents, add new colors to the industry, and open up a new path in the path of research and development.
    Toxicity Research
    Recently, I have focused on the toxicity study of the chemical "1- (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone".
    After many experimental investigations, the subjects were administered at an appropriate sample dose under a specific experimental environment. Observe their reactions and observe changes in their physiological characteristics. At the beginning, the subjects' behavior did not show significant abnormalities, but after a while, they gradually became depressed and their activity decreased.
    After in-depth analysis, it was found that this chemical seemed to interfere with the metabolic pathways in the subjects, involving some key physiological functions. It seems to have an inhibitory effect on the activity of specific cells, which in turn affects the overall physiological operation. Although the research is still in the preliminary stage, it can be inferred that "1- (3 - Iodo - 1 - Isopropyl - 1H - Pyrazol - 4 - Yl) Ethanone" has a certain toxicity, and more detailed and in-depth studies are needed to clarify its toxicity and mechanism of action, and provide a solid basis for preventing its potential harm.
    Future Prospects
    Looking at today's world, science and technology are prosperous, and chemical things are changing with each passing day. I am focusing on the research of (1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone.
    Although what we have obtained now has seen initial success, there is still a great way to expand in the future. I expect that in the field of medicine, with its unique structure, we may be able to find new paths, develop special drugs, and solve people's diseases. In industry, it is also expected to use its characteristics to optimize production and improve quality.
    And the road of scientific research is endless. When we continue to study, improve our skills, or be able to penetrate deeper mysteries at the molecular level, the potential of (1- (3-Iodo-1-Isopropyl-1H-Pyrazol-4-Yl) Ethanone) will be fully stimulated. At that time, to benefit the common people and promote the industry forward, it must be a lie, and the future prosperity can be awaited.
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    Frequently Asked Questions

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    What are the chemical properties of 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone?
    1 - (3-alkynyl-1-isobutyl-1H-pyrazole-4-yl) acetic acid is an organic compound. In terms of its chemical properties, from the perspective of structure, there are different functional groups such as alkynyl, pyrazolyl and carboxyl in the molecule, and each functional group endows the compound with various reactivity.
    As an unsaturated bond, the alkynyl group has typical unsaturated bond properties. It can undergo an addition reaction, such as with hydrogen under the action of a suitable catalyst, it can be gradually hydrogenated to form olefins first, and then alkanes; it can undergo electrophilic addition with halogen elements (such as bromine), so that the reddish-brown of bromine fades, generating products containing bromine substitution; when encountering hydrogen halides, follow the Markov rule or anti-Markov rule for addition, and obtain different regionally selective products under different conditions. Because alkynyl carbons are hybridized by sp, their hydrogen atoms have a certain acidity. Under the action of strong bases (such as sodium amide), protons can be taken away to generate alkynyl negative ions. This alkynyl negative ions can participate in nucleophilic substitution reactions as nucleophiles, and react with halogenated hydrocarbons to generate carbon-carbon bond growth products.
    pyrazolyl is a nitrogen-containing heterocycle with certain aromaticity. The nitrogen atom on the pyrazole ring has lone pair electrons, which makes it participate in the reaction as an electron donor, and can form complexes with metal ions, which is widely used in the field of materials chemistry. Due to the electronegativity of nitrogen atoms, hydrogen atoms at different positions on the pyrazole ring have different acidity. Under appropriate conditions, electrophilic substitution reactions can occur, such as halogenation, nitrification, sulfonation, etc. The substitution positions are jointly affected by the electron cloud distribution of the pyrazole ring and the localization effect of the substituent.
    Carboxyl group is another important functional group of this compound, which is acidic. It can partially ionize hydrogen ions in aqueous solution, making the solution acidic, and can neutralize with bases to form carboxylate and water. Carboxyl groups can be esterified with alcohols catalyzed by concentrated sulfuric acid and heated to form ester compounds with fruit flavor, which is a reversible reaction. In addition, carboxyl groups can also undergo dehydration reactions to form acid anhydrides, or react with ammonia (amine) to form amides.
    These functional groups interact with each other, so that 1- (3-alkyne-1-isobutyl-1H-pyrazole-4-yl) acetic acid has rich chemical properties and has potential application value in organic synthesis, medicinal chemistry and other fields.
    What are the synthesis methods of 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone?
    To prepare 1- (3-thio-1-isobutyl-1H-pyrazole-4-yl) acetic acid, there are many synthesis methods.
    First, it can be initiated by halogenation reaction. Select a suitable halogenated reagent to halogenate the specific position of the thiazole derivative, and then introduce isobutyl through nucleophilic substitution reaction, followed by pyrazole cyclization, and then carboxylation reaction to obtain the target product. This way, the halogenation conditions need to be carefully selected to prevent side reactions and ensure the precise positioning of halogen atoms. When nucleophilic substitution, pay attention to the reagent activity and reaction temperature to avoid over-reaction or substitution check point deviation.
    Second, the pyrazole derivative is used as the starting material. The pyrazole ring is modified, a suitable substituent is introduced, and the target molecular skeleton is constructed by reacting with the reagent containing the thiazole structure. The key to this process is the modification step of the pyrazole ring. According to the structure of the target product, the reaction sequence and conditions are precisely designed to ensure the accurate introduction of the substituent into the check point.
    Third, the metal catalytic coupling reaction can be used. Select a suitable metal catalyst, such as palladium, nickel, etc. Using thiazole derivatives containing halogen atoms and pyrazole derivatives containing alkenyl or alkynyl groups as raw materials, a carbon-carbon bond is formed through a coupling reaction. After further reaction, carboxyl groups are introduced and substituents are adjusted to obtain the target product. Metal catalytic coupling requires strict control of catalyst dosage, ligand selection and reaction environment to improve reaction efficiency and selectivity.
    Synthesis of this compound, each method has its own advantages and disadvantages. It is necessary to comprehensively weigh and choose the optimal path according to the actual situation, such as raw material availability, cost, controllability of reaction conditions, etc., to obtain the target product efficiently.
    In what fields is 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone used?
    1- (3-cyano- 1-isobutyl-1H-pyrazole-4-yl) acetic acid, this compound is used in medicine, pesticides and other fields.
    In the field of medicine, this compound may have specific biological activities and can act as an intermediate for drug synthesis. The structure of pyrazole and cyanyl often imparts unique physiological activities to compounds, or can be modified and modified to make them fit specific drug targets, and then used to develop drugs for the treatment of specific diseases, such as anti-tumor, anti-inflammatory, antibacterial drugs, etc. For example, some anti-tumor drugs can inhibit the growth and proliferation of tumor cells by precisely designing such structural units.
    In the field of pesticides, this compound can be used as a key intermediate for the creation of new pesticides. The structure composed of pyrazole and cyanyl groups may give it good insecticidal and bactericidal activities. For example, after rational structure optimization, high-efficiency pesticides targeting specific pests or pathogens can be developed, providing a powerful means for agricultural pest control, which can not only improve crop yield and quality, but also reduce environmental pollution caused by the use of traditional pesticides.
    With its unique chemical structure, this compound has shown broad application prospects in the fields of medicine and pesticide research and development. Scientists can continue to explore and innovate to develop more efficient and low-toxicity products.
    What is the market outlook for 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone?
    The current market prospect of 1- (3-cyano- 1-isobutyl-1H-pyrazole-4-yl) acetic acid can be described as complex and variable.
    From the perspective of its characteristics, this compound may have extraordinary potential in the field of pharmaceutical research and development. Due to its unique structure or interaction with specific biological targets, it provides an opportunity for the creation of new drugs. In the treatment research of certain diseases, its chemical activity may help to develop targeted drugs, which is a great advantage and adds a bright color to the market prospect.
    However, the market prospect is also constrained by many factors. The first to bear the brunt is regulations and policies. Drug regulatory authorities have strict requirements for the approval of new drug research and development. From pre-clinical research to clinical trials, there are layers of checkpoints, and any mistakes in any link may delay or even terminate the research and development process. If this compound is to be converted into a marketed drug, it needs to go through a long and arduous approval process, which is time-consuming and laborious, and costs have skyrocketed, which poses a severe challenge to market expansion.
    Furthermore, the competitive situation cannot be underestimated. In the field of pharmaceutical research and development, hundreds of schools of thought contend, and many scientific research institutions and pharmaceutical companies are engaged in innovative drug research and development. There may be similar compounds or more advantageous alternatives developed at the same time. If they are launched first and occupy the market share, the market space of 1- (3-cyano-1-isobutyl-1H-pyrazole-4-yl) acetic acid may be greatly squeezed.
    And market demand is also the key. Although the potential therapeutic value is quite high, if the corresponding disease patient population is limited, or there are mature treatment options, its market size will be difficult to expand significantly. Only by accurately positioning the market demand can we target and develop the market.
    In summary, although 1- (3-cyano-1-isobutyl-1H-pyrazole-4-yl) acetic acid has potential, the market outlook is cloudy, and opportunities and challenges coexist. Only by responding prudently can we gain a place in the market wave.
    What are the upstream and downstream products of 1- (3-iodine-1-isopropyl-1H-pyrazole-4-yl) ethyl ketone?
    1- (3-cyano- 1-isobutyl-1H-pyrazole-4-yl) acetic acid, there are many upstream and downstream products of this compound.
    The upstream product is the raw material required for its preparation. For example, the preparation of 1- (3-cyano- 1-isobutyl-1H-pyrazole-4-yl) acetic acid often requires specific pyrazole compounds as starting materials. It may involve cyano- containing pyrazole derivatives, which introduce isobutyl into the 1-position of the pyrazole ring through a series of reactions to obtain key intermediates. This process may require the nucleophilic substitution reaction of halogenated isobutane with pyrazole derivatives under basic conditions to achieve the synthesis of 1-isobutyl-3-cyano-pyrazole.
    The downstream product is the product of further reaction of 1- (3-cyano-1-isobutyl-1H-pyrazole-4-yl) acetic acid as a raw material. In the field of organic synthesis, it can be used as a key intermediate to participate in the construction of more complex heterocyclic compounds. For example, esterification reactions with specific alcohols under the action of catalysts generate corresponding ester derivatives, which may exhibit unique biological activities in medicinal chemistry and provide potential lead compounds for the development of new drugs. Or, the carboxyl group of the compound can be amidated with amines to form amide products. Such amides may have applications in materials science, drug delivery systems, etc., such as as monomers for building polymer materials with special properties, or key structural units for designing targeted drug delivery vehicles.