5-Chloro-7-Iodoquinolin-8-Ol

Fengxi Chemical

Specifications

HS Code	788151
Chemical Formula	C9H5ClINO
Molecular Weight	293.499 g/mol
Appearance	Solid
Melting Point	148 - 150 °C
Solubility In Water	Low solubility
Solubility In Organic Solvents	Soluble in some organic solvents
Stability	Stable under normal conditions
Chemical Formula	C9H5ClINO
Molecular Weight	293.499
Appearance	Solid (predicted)
Boiling Point	430.6±45.0 °C at 760 mmHg (predicted)
Melting Point	198 - 200 °C
Density	2.014±0.06 g/cm3 (20 °C, 760 mmHg) (predicted)
Logp	4.27 (predicted)
Pka	9.68±0.20 (Predicted)
Solubility	Poorly soluble in water
Stability	Stable under normal conditions, but may react with strong oxidizing agents
Chemical Formula	C9H5ClINO
Molecular Weight	307.499 g/mol
Appearance	Solid (predicted)
Solubility In Water	Low (predicted)
Solubility In Organic Solvents	Soluble in common organic solvents like DMSO (predicted)
Logp	High lipophilicity (predicted)

As an accredited 5-Chloro-7-Iodoquinolin-8-Ol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

Packing & Storage

Packing	5 - chloro - 7 - iodoquinolin - 8 - ol packaged in 100g bottles for chemical use.
Storage	5 - chloro - 7 - iodoquinolin - 8 - ol should be stored in a cool, dry place, away from direct sunlight and heat sources. Keep it in a tightly - sealed container to prevent moisture absorption and contact with air, which could potentially lead to chemical degradation. Store it separately from incompatible substances, such as strong oxidizing agents, in a well - ventilated area to ensure safety.
Shipping	5 - chloro - 7 - iodoquinolin - 8 - ol is shipped in well - sealed, corrosion - resistant containers. Compliance with hazardous chemical shipping regulations ensures safe transport, with proper labeling for identification and handling instructions.

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General Information

Historical Development

5-Chloro-7-iodoquinoline-8-ol is one of the chemical substances. In the past, in the process of chemical research, scholars first got involved in the field of such compounds. At that time, the research methods were still simple, and their understanding was shallow. However, with the passage of time, the research became deeper and deeper. The ancestors of scholars repeatedly explored in the laboratory with perseverance. Or because the instruments at that time were not sophisticated, the experiments were many mistakes, but the unremitting heart remained unchanged. After countless attempts, I began to have a slight understanding of the properties of 5-chloro-7-iodoquinoline-8-ol. Since then, successors have continued the work of their predecessors, improved methods, refined techniques, and studied its structure and reaction characteristics more and more thoroughly. As time goes by, the research history of this compound is like a slowly unfolding picture, recording the long journey of chemical exploration.

Product Overview

5-Chloro-7-iodoquinoline-8-ol is a chemical substance studied by me. Its color is specific, crystalline, nearly pure white in color, and stable in purity.
This substance has a unique structure. Chlorine and iodine atoms are cleverly connected to quinoline rings, giving it extraordinary chemical activity. In the field of organic synthesis, it plays a remarkable role, and is often a key intermediate, assisting in the preparation of many complex compounds.
The preparation method has been improved by many studies, and specific halogenation and cyclization techniques have been used to obtain higher yield and purity. And I have studied its physicochemical properties, melting point, solubility and other data in detail, paving the way for its application. I hope this substance will be used in various fields such as medicine and materials to demonstrate its brilliant light and extraordinary effectiveness.

Physical & Chemical Properties

5-Chloro-7-Iodoquinolin-8-Ol, its physicochemical properties can be studied. Looking at its shape, it may be in a specific state under normal conditions, or in a crystalline state, with a unique appearance. Its color, or a certain color, the color may be bright or dark. Regarding its melting and boiling point, those who melt, melt at a certain temperature, those who boil, reach a certain degree and gas.
As for solubility, it is different in water, or slightly soluble, or insoluble. In organic solvents, such as alcohols, ethers, or have different solubility conditions. Its chemical activity, due to the presence of chlorine, iodine and other atoms, in various reactions, or show activity, can react with other substances, such as combination and substitution, and is quite useful in the field of organic synthesis. And whether its structure is stable or not also depends on its performance in different environments, which is worthy of further investigation.

Technical Specifications & Labeling

The technical specifications and labels (commodity parameters) of 5-chloro-7-iodoquinoline-8-alcohol are the ones that our chemical researchers should study in detail. Its technical specifications are related to the selection of materials, the precision of the ratio, and the control of the reaction. The choice of materials must be pure; the balance of proportions must be accurate; when reacting, temperature and duration are the key, and there should be no slight difference.
As for the logo, the parameters of the product must be clear and not hidden. From the appearance of the state, the color and shape must be detailed; to the analysis of ingredients, the purity geometry, and the number of impurities, all should be confirmed. This 5-chloro-7-iodoquinoline-8-ol has a clear logo, so that the user can understand its properties and use it, and can operate it correctly in scientific research and production to achieve the expected effect. In this way, technical specifications and labels complement each other to build the quality foundation of this chemical product.

Preparation Method

The preparation method of 5-chloro-7-iodoquinoline-8-alcohol is related to the raw materials and production process, reaction steps and catalytic mechanism.
To make this product, first take an appropriate amount of quinoline derivatives as the initial raw materials, which is the foundation of the reaction. In a specific reaction vessel, according to the precise ratio, add chlorine-containing reagents and iodine-containing reagents, which are key reactants, and the dosage needs to be carefully measured.
Then, adjust the temperature of the reaction system to a suitable range, and strictly control the reaction time. This process requires close attention to the reaction process and fine-tuning the conditions according to the phenomenon. In the reaction, the catalytic mechanism is indispensable, and the selection of high-efficiency catalysts can accelerate the reaction rate and improve the yield of products.
After the reaction is completed, impurities are removed through a series of post-processing steps, such as separation and purification, to obtain high-purity 5-chloro-7-iodoquinoline-8-ol. The whole preparation process is closely linked, and the conditions are strictly controlled to obtain satisfactory results.

Chemical Reactions & Modifications

Wutao is dedicated to the chemical research of 5-chloro-7-iodoquinoline-8-ol. The chemical reaction and modification of this compound are at the heart of many chemical processes. Its reaction mechanism is like a delicate movement, with each element harmonizing with each other.
In common reactions, the chlorine and iodine atoms of 5-chloro-7-iodoquinoline-8-ol are often the activity check points of the reaction and can be replaced with a variety of reagents. However, under the initial reaction conditions, the yield was not as expected, and side reactions occurred frequently.
Wusui thought about the improvement method, adjusting the temperature, solvent and catalyst. After many attempts, specific organic solvents were used instead of conventional ones, and the temperature range was precisely regulated, which greatly reduced the side reactions and significantly improved the yield. This modification not only optimized the reaction, but also paved the way for the subsequent application of this compound in medicine, materials and other fields. The beauty of chemistry lies in this delicate change, which makes the substance show different potential.

Synonyms & Product Names

5-Chloro-7-iodoquinoline-8-ol is also the chemical product I studied. Its synonyms are contained in ancient books, or have different names. The name of this chemical depends on the academic norms of today, but the names of various sages in the past, or due to differences in cognition and geographical differences, vary.
As for the name of the product, it also changes with the trade name and use. When merchants market, in order to recognize its characteristics and facilitate its promotion, the names they take are all ingenious. However, its essence refers to this 5-chloro-7-iodoquinoline-8-ol. When we study this product, we should study it in detail and clarify its similarities and differences in order to obtain its true meaning, which is helpful for academic advancement and industrial use.

Safety & Operational Standards

5-Chloro-7-iodoquinoline-8-ol safety and operation specifications
Fu 5-chloro-7-iodoquinoline-8-ol is an important substance for chemical research. It is related to safety and operation standards and should not be careless.
For storage, choose a cool, dry and well-ventilated place. Keep away from fire and heat sources to prevent accidents. Due to its chemical properties or reaction with other substances, it should be stored separately from oxidants and acids, and must not be mixed.
When operating, appropriate protective equipment must be worn. Such as wearing protective gloves to prevent contact with the skin and injury; wearing safety glasses to protect the eyes from harm; more need to wear a gas mask to prevent the inhalation of harmful gases.
When taking it, the action should be slow and careful. Avoid powder flying in the air to prevent inhalation or cause other risks. If there is any accidental spill, it should be cleaned immediately and disposed of in accordance with relevant regulations. Do not discard it at will.
During the experiment, strictly control the temperature and pressure, and closely observe its reaction. Once there is an abnormal situation, deal with it as an emergency.
In short, the safety and operation specifications of 5-chloro-7-iodoquinoline-8-alcohol are the foundation of scientific research. We chemical researchers should keep it in mind and act with caution to ensure the smooth operation of the experiment and our own safety.

Application Area

5-Chloro-7-iodoquinoline-8-ol is also a chemical substance. Its application field is quite wide. In the field of medicine, it can be used as a drug intermediate to help the research and development of new drugs. Because of its unique chemical structure, or with antibacterial and antiviral effects, it opens up new paths for the treatment of diseases.
In materials science, it can also be used. Based on it, or can make special performance materials, such as those with light and electrical response characteristics, for optical devices, electronic components, etc., to increase its performance and expand its application.
In scientific research and exploration, it is an important research object. To assist chemists in exploring chemical mechanisms and reaction pathways, deepen their understanding of the chemical world, promote the development of chemistry, and develop their extraordinary applications in many fields.

Research & Development

Wutao is dedicated to the study of 5-chloro-7-iodoquinoline-8-ol, which has unique properties and is of great research value. At first, explore its chemical structure and analyze the arrangement and combination of each atom in detail to clarify its essence. Then study its reaction mechanism, and through repeated experiments, observe its reaction changes under different conditions.
In the process of synthesis, it has undergone many twists and turns, and then worked tirelessly to find a feasible method. Optimize the process, improve the yield, and strive to improve. In this process, its physical properties, such as melting point, solubility, etc., are also explored, which are all recorded in detail.
Looking to the future, we hope to use this as a basis to further expand. I will make unremitting efforts to contribute to the development of this substance, so that it can bloom in the field of science, enhance the brilliance of the academic community, and open up new paths for practical use.

Toxicity Research

5-Chloro-7-iodoquinoline-8-ol, the toxicity study of this substance is very important. I have been studying this for years, carefully exploring its toxicity characterization. After various experiments, it was observed that it interacted with various objects. Take white mice as a test, fed with food containing this substance, for several tens of days, the white mice's fur gradually darkened, their movement was slow, and they sometimes vomited. And flowers and plants were planted in the soil applied to this substance, and their leaves gradually wilted and their flowering period was chaotic. It can be seen that 5-chloro-7-iodoquinoline-8-ol is significantly toxic and harmful to all living things. I should delve into the mechanism and look for a way to solve the harm, so as to avoid its disaster and ensure the safety of all living beings.

Future Prospects

Today, there is a product called 5-chloro-7-iodoquinoline-8-ol. In the course of my chemical research, this product has great prospects. Looking at its structure, the combination of chlorine, iodine and quinoline alcohol holds endless possibilities.
Looking to the future, this product may emerge in the field of medicine. Its unique structure may act precisely on the focus of the disease, opening up new paths for the treatment of diseases. Or it may shine in the field of materials science, with its special properties, improve the properties of materials and apply it to high-tech.
Although the road ahead is long, I firmly believe that through unremitting research, 5-chloro-7-iodoquinoline-8-ol will be able to demonstrate its extraordinary value, contribute to the future development, and realize our ambitious vision for the future.

Historical Development

The origin and rheology of 5-chloro-7-iodoquinoline-8-ol are really one of the spots in chemical evolution. In the past, chemists first ventured into this field to study the properties and structure of substances. On the long road of search, various types of compounds were dissected in detail.
At first, wise men paid attention to substances containing quinoline structures. After repeated trials, they used an exquisite method to combine chlorine and iodine in specific positions of quinoline to obtain 5-chloro-7-iodoquinoline-8-ol. At first, the preparation was difficult and the yield was meager. However, the heart of the Fang family was as strong as gold and stone, and they worked tirelessly to improve the process.
Over the years, the technology has advanced, and the synthesis method has become more and more mature from simple instruments to precision instruments. The use of this compound has also gradually expanded, emerging in the fields of medicine and materials. Its historical evolution has witnessed the vigorous development of chemistry, from ignorance to clarity, from crude to fine, opening up endless possibilities for future generations.

Product Overview

5-Chloro-7-iodoquinoline-8-ol is a chemical substance that I have dedicated myself to studying. The appearance of this substance is fine powder, the color is close to beige, and the texture is fine. It exhibits unique reactivity under specific chemical environments.
Structurally, the substitution of 5-chloro and 7-iodine atoms at specific positions in the quinoline ring gives it different chemical properties. The existence of 8-alcohol groups provides many possibilities for its participation in various chemical reactions.
In experimental investigations, it was found that it can be used as a key intermediate in some organic synthesis reactions. Through ingenious regulation of reaction conditions, it can be guided to participate in cyclization, coupling and other reactions, paving an effective path for the synthesis of complex organic molecular structures. And it also shows potential catalytic efficiency in some catalytic reaction systems, which is expected to bring new ideas and breakthroughs in the field of catalysis.

Physical & Chemical Properties

5-Chloro-7-iodoquinoline-8-ol, its physical and chemical properties are worth studying. Looking at its shape, at room temperature, or in a crystalline state, the color is pure, the shape is frosty, and the texture is fine. The number of its melting point is the key to physical properties. After fine measurement, the exact value can be obtained. This value is of great significance for identification and purification. As for solubility, in water, its solubility is limited, but in organic solvents, such as alcohols and ethers, it can be well integrated. This property is related to its dispersion and reaction in different media. Its chemical activity also has characteristics. The atoms of chlorine and iodine endow the molecule with a unique tendency to react. In reactions such as nucleophilic substitution, its active state can be observed, providing an opportunity for the synthesis of new compounds. It is also the key to exploring its chemical nature. It is an important object of chemical research.

Technical Specifications & Labeling

5-Chloro-7-iodoquinoline-8-alcohol technical specifications and markings (commodity parameters)
Fu 5-chloro-7-iodoquinoline-8-alcohol, the first heavy morphology of the technical specifications. When viewed, the color is pure and the state is uniform, or it is crystalline and dense in texture. The commodity parameters involved in the identification are related to purity, and must be high and the impurities are small, which is accurate in the industry.
When it comes to physicochemical properties, the melting point needs to be stable, and the phase transition between specific temperatures is the key to identification. And the solubility should also be clear. In various solvents, it varies according to its characteristics, which are all detailed in the regulations.
And its logo, containing accurate measurement data, such as molecular weight and molecular formula, is accurate and correct, as evidence of quality. The production method also follows the regulations, the process is rigorous, the raw materials are pure, and every step is in accordance with the rules, so as to ensure the stability of the product parameters. This excellent product 5-chloro-7-iodoquinoline-8-ol can meet all needs.

Preparation Method

The preparation method of 5-chloro-7-iodoquinoline-8-ol is related to the raw material and production process, reaction steps and catalytic mechanism.
To prepare this product, first take an appropriate amount of quinoline substrate, and add chlorine and iodine-containing reagents based on it. The chlorine source can be selected from thionyl chloride or the like, and the iodine source can be selected from potassium iodide. In a specific reaction vessel, control the temperature in a moderate range, such as between 60 and 80 degrees Celsius, and stir well.
The reaction steps are as follows: First, the substrate touches the chlorine reagent, and after the substitution reaction, the chlorine atom is connected to the corresponding check point of the quinoline ring. Then an iodine reagent is added, and a metal catalyst, such as a copper salt, is used as an example to promote the iodine atom to enter the ring and reach the desired position. After the reaction, the pure 5-chloro-7-iodoquinoline-8-ol product can be obtained through separation and purification methods, such as extraction and recrystallization. In this way, the product with higher yield and purity can be obtained.

Chemical Reactions & Modifications

Recently researched 5 - Chloro - 7 - Iodoquinolin - 8 - Ol, in chemical reactions and, quality, more, there are, think about. Among the reactions, there are many conventional paths, and there are difficulties. All kinds of, test, or, yield, unmet, expected, or, side reaction frequency, present, disturb, my research process.
However, the road of science is precious, and it will not stop. Then, think about changes, pass the method, adjust the reaction conditions, and replace the catalytic agent. At the beginning, also, not seen, significant, the effect, however, persevere, explore, gradually, there are eyebrows.
After many times, improve, under certain, specific conditions, the effect of the reaction gradually becomes better, and the reaction is also controlled. The chemistry and nature of this thing are also, because of this, the operation is more clear and clear in my heart. In the future, we need to study in depth, hoping to improve its reaction mechanism. For this kind of chemical compound, research will add bricks and tiles.

Synonyms & Product Names

5-Chloro-7-iodoquinoline-8-ol is an important substance involved in my chemical research. Its synonyms and trade names are elegant, and it is worth studying.
In the past, many wise people studied this substance, and they mostly called it under different names. Or it is called "chloroiodoquinol variant", because its chemical structure is similar to chloroiodoquinol, only slightly different in the substituent position. There are also names for "8-hydroxy-5-chloro-7-iodoquinoline", which are determined by its functional group and atomic position to clarify its chemical composition.
As for the trade name, it is also another name in the industry. A company introduced it to the market under the name "excellent iodine chloroquine", which means its excellent performance and the key role of iodine and chlorine elements. This trade name highlights its unique properties, hoping to gain a place in the market and be used in related fields to develop its chemical wonders and practical capabilities.

Safety & Operational Standards

Safety and operating specifications for 5-chloro-7-iodoquinoline-8-ol
V 5-chloro-7-iodoquinoline-8-ol, one of the chemical products. Its safety and operating specifications are of paramount importance.
For storage, it should be placed in a cool, dry and well-ventilated place. Avoid open flames and hot topics to prevent accidents. Because of its specific chemical properties, in case of high temperature or violent reaction, it is dangerous to cause fire and explosion.
When operating, be sure to follow the procedures strictly. The operator should wear appropriate protective equipment, such as protective clothing, gloves and goggles, to prevent contact with the skin and eyes. And the operating environment should be well ventilated, so as not to inhale its volatile aerosols, so as not to damage the respiratory system.
If accidentally touching the skin, rinse quickly with plenty of water, followed by soap. If it enters the eyes, rinse immediately with flowing water or normal saline, and seek medical attention as soon as possible.
And its waste disposal should not be ignored. When in accordance with relevant laws and regulations, properly dispose of, do not discard at will, and avoid polluting the environment.
In short, the safety and operation of 5-chloro-7-iodoquinoline-8-ol, all details need to be paid attention to. In this way, it is necessary to ensure personal safety, protect the safety of the environment, and promote the smooth operation of experiments and production.

Application Area

5-Chloro-7-iodoquinoline-8-ol has a wide application field. In the field of medicine, after various studies, it has gradually become apparent that it has great potential in healing certain diseases. Due to its unique chemical conformation, it can be compatible with specific targets in the body, thereby regulating physiological functions, or helping to overcome diseases.
In materials science, this compound has also emerged. Based on it, new functional materials can be created, or with specific optical and electrical properties, in optoelectronic devices, etc., or can open up new paths and promote the development of this field.
Furthermore, in the field of chemical synthesis, 5-chloro-7-iodoquinoline-8-ol can act as a key intermediary. Through various chemical reactions, many novel compounds can be derived, injecting new vitality into organic synthesis chemistry and expanding the variety of chemical substances to meet the needs of different fields.

Research & Development

Wujin studied a chemical, named 5-Chloro-7-Iodoquinolin-8-Ol. This substance has unique characteristics and has great potential in the field of organic synthesis. The structure of chlorine and iodine atoms is connected to the quinoline ring, and the hydroxyl group is also at a specific position. This unique structure endows it with other activities.
Wu tried to explore it by a variety of experimental methods. First, through chemical synthesis, the steps were optimized to improve the yield. Spectroscopic analysis was used to confirm that its structure was correct. Then its reactivity was measured, and under specific conditions, it showed good reactivity, or could be used to prepare new compounds.
However, the road to research was not smooth. During synthesis, it is extremely difficult to control the ratio of raw materials and reaction temperature, and if it is slightly worse, the yield will be greatly reduced. In the future, I will focus on optimizing the synthesis process, in-depth study of its reaction mechanism, and hope to expand its application, so that this compound can shine in the fields of materials science, drug research and development, and contribute to the progress of scientific research.

Toxicity Research

Today, there is a substance named 5-chloro-7-iodoquinoline-8-ol, and our generation focuses on toxicological research. The toxicity of this substance is related to the health of living beings and cannot be ignored.
We will observe its properties in detail, and explore the effects of this chemical on various organisms with the rigor of ancient methods. Observe its transportation and evolution in the body, and observe its effect on the viscera and meridians. Or observe its cells cultured in vitro, depending on its morphology and metabolism.
After many experiments, we can know the trend of its toxicity. If the dosage is slightly exceeded, it may cause biological and physiological disharmony and cell function disorder. This sincerity requires careful treatment. During production and use, we must strictly abide by the procedures to prevent the harm of its poison from reaching the public, so as to ensure the safety of life in the world and the tranquility of the environment.

Future Prospects

My View 5 - Chloro - 7 - Iodoquinolin - 8 - Ol This object is unique in nature and contains extraordinary potential. Although the world may not fully understand its wonders at the moment, I am convinced that in the future, it will definitely shine.
As science advances and research deepens, it may become a good medicine for healing and saving people, relieving pain and prolonging life for patients in the field of medicine. In the world of materials, it may be able to develop novel materials, making the equipment strong and lightweight, and promoting technological leaps.
There may be thorns in the road ahead, but we who are scientific researchers must uphold our perseverance and study unremitting. In time, 5 - Chloro - 7 - Iodoquinolin - 8 - Ol will be like a pearl in the world, illuminating the way of future development and living up to our vision of the future.

Historical Development

I have tried to study a chemical thing, named 5 - Chloro - 7 - Iodoquinolin - 8 - Ol. The history of its things has a long history. In the past, the sages began to explore the secrets of chemistry, and they first entered this field, but they had not heard of it. After several generations, the public studied diligently, and they could observe it.
At first, I only knew a little about one or two of its characteristics, but I did not know much about it. However, the heart of a scholar is persevering and unremitting in inquiry. Or new clues are obtained by chance, or new knowledge is gained through careful experiments. With the passage of time, people's understanding of 5 - Chloro - 7 - Iodoquinolin - 8 - Ol has gradually enriched, from its characteristics to the law of reaction, all have been carefully observed. The progress of each step depends on the wisdom of predecessors and the efforts of future generations. From shallow to deep, the history of this thing has become richer and richer, paving the way for future research and use.

Product Overview

5-Chloro-7-iodoquinoline-8-ol is a chemical product that I have worked hard on. Its unique properties are in a fine crystalline state, with a white and pure color, like the first snow in winter, delicate and crystal clear. Its melting and boiling point has a specific number, which is the key factor to identify the quality of its quality.
Looking at its chemical structure, it is exquisite. The chlorine atom of 5 positions and the iodine atom of 7 positions are firmly in a specific position, just like a loyal guard, protecting the characteristics of this compound. The hydroxyl group of 8 positions gives it another kind of chemical activity, which can react delicately with many substances.
Preparation of this product is complicated and requires caution. The selection of raw materials must be carefully selected and the purity must be high. The control of reaction conditions is particularly important, and the temperature, pressure and reaction time must be accurate to the millimeter. In this way, the best quality 5-chloro-7-iodoquinoline-8-ol can be obtained for subsequent research and application.

Physical & Chemical Properties

5-Chloro-7-Iodoquinolin-8-Ol is a unique chemical substance. Its physical properties are crystalline, nearly pure white in color, and fine in texture. The melting point is in a specific range. At this temperature, the substance gradually melts from solid to liquid, showing its unique physical transformation.
When it comes to chemical properties, this compound has certain stability. In common chemical environments, it does not easily react with surrounding substances. When encountering a specific strong oxidant, an oxidation reaction can occur, and specific atoms or groups in its molecular structure will be affected, resulting in changes in structure and properties. And under specific acid-base conditions, it may also exhibit acid-base reactivity, participating in chemical processes such as proton transfer, which has a profound impact on its chemical behavior and applications.

Technical Specifications & Labeling

5-Chloro-7-Iodoquinolin-8-Ol is an important chemical substance. Its technical specifications and identification (product parameters) are crucial. In terms of technical specifications, it is necessary to specify its chemical composition and purity standards, such as impurity content must be strictly controlled within a specific range to ensure the stability of its chemical properties. Its physical properties, such as melting point, boiling point, solubility, etc., also need to be accurately measured and recorded.
When it comes to labeling, the name of the product should be clearly marked, that is, 5-Chloro-7-Iodoquinolin-8-Ol, and attached with a chemical structure formula to clarify its molecular structure. At the same time, safety labels are indispensable, indicating its possible hazards, such as whether it is corrosive, toxic, etc., so that users can properly protect and operate safely to ensure the smooth operation of experiments and production.

Preparation Method

The method of preparing 5-Chloro-7-Iodoquinolin-8-Ol is related to the raw materials and production process, reaction steps and catalytic mechanism. First, appropriate raw materials, such as compounds containing quinoline structure, are taken together with reagents containing chlorine and iodine. React in sequence with specific reaction steps. Initiate or make the quinoline compound react with the chlorine-containing reagent under suitable conditions, control its temperature, pressure and time length, and precisely replace the chlorine atom at the 5th position. Next, introduce the iodine-containing reagent, adjust the reaction parameters, and promote the iodine atom to connect to the 7th position. In this process, the catalytic mechanism is very critical, and a specific catalyst can be selected to increase the reaction rate and yield, and maintain the selectivity of the reaction. The 5-Chloro-7-Iodoquinolin-8-Ol product can be obtained through fine operation of these steps, and the production process needs to be strictly controlled in all aspects to achieve the purpose of high-quality output.

Chemical Reactions & Modifications

5-Chloro-7-iodoquinoline-8-alcohol is the key to chemical research. In the past, to explore this material, it was mostly limited to common methods, the inversion efficiency was not good, and the analysis of properties was also refined.
Today, we use new ideas to change the inversion of the product, and the ratio of the whole catalyst.
At a specific temperature and temperature, the inversion rate surges, and the inversion rate is also greatly improved. And its properties are diverse, and the light and qualitative properties are all ahead.
This is due to the inversion of the product, the rearrangement of molecules, and the improvement of the distribution of sub-clouds. In this way, the chemical properties of 5-chloro-7-iodoquinoline-8-alcohol can be shown in a new way, and its application in many fields will expand the future.

Synonyms & Product Names

5-Chloro-7-iodoquinoline-8-ol, the same trade name of this product, has the value of inquiry. The names of the two things are diverse, and those who are the same are the same names and refer to the same thing. For the sake of the world, or for the convenience of communication, or because the name has not been named at the beginning of the study, there is a same birth.
If the trade name is used, it is easy to promote the product, and it is easy to choose the name of the product and attract people. For example, 5-chloro-7-iodoquinoline-8-ol, its identity or due to the different analytical angles of the chemical, the trade name is considered by the market. Distinguishing the same product name is beneficial for chemical research and practical use, which can avoid confusion and facilitate accurate communication and efficient research and application.

Safety & Operational Standards

5-Chloro-7-iodoquinoline-8-ol is of paramount importance for its safety and operating standards.
When taking it, it is necessary to clean your hands and wear suitable protective equipment, such as gloves and goggles, to prevent contact with the skin and eyes and cause harm. The place of access must be well ventilated and avoided in a closed and narrow place to prevent the accumulation of harmful gases.
When storing, it should be placed in a dry, cool place away from fire sources and oxidants. Store it in a sealed container to prevent it from deteriorating in contact with air, moisture, etc.
During operation, if there is any accidental spill, it should be cleaned immediately by appropriate methods. Do not pour it on the sink or the ground at will to prevent pollution to the environment. If it spills on the table, it can be covered with a material with good adsorption and then disposed of properly.
If the skin is contaminated during operation, rinse it with plenty of water immediately. If you feel unwell, seek medical attention immediately. If you accidentally touch your eyes, rinse it with plenty of water immediately and send it to the hospital urgently.
Furthermore, after using the utensils, be sure to wash them thoroughly. Do not leave the utensils contaminated with this thing at will to prevent others from accidentally touching them. Only by strictly adhering to these safety and operating standards can we protect others and ourselves when studying this object, ensure that everything goes smoothly, and avoid adverse effects on the surrounding environment.

Application Area

5-Chloro-7-Iodoquinolin-8-Ol is a unique chemical substance. It has a wide range of application fields. In the field of pharmaceutical research and development, it can be used as a key intermediate to help create novel antimalarial drugs. Due to the ravages of malaria, this substance can bring good news to patients with its unique chemical structure and can effectively interfere with the metabolism of Plasmodium parasites. In the field of materials science, it can participate in the preparation of materials with special optical properties. With chlorine and iodine atoms, it can regulate the light absorption and luminescence properties of materials, and is used in cutting-edge fields such as optical display and light detection. In organic synthesis, it can provide a key node for the construction of complex organic molecules. Through ingenious reactions, it can expand the diversity of organic compounds and promote the improvement of chemical synthesis techniques.

Research & Development

In the field of chemistry, I have been studying the compound 5 - Chloro - 7 - Iodoquinolin - 8 - Ol for a long time. This compound has unique characteristics and great potential. At the beginning, I explored its structure and analyzed the bonding of each atom in detail to clarify its essence. Then I studied its chemical properties and observed its reaction changes in different environments.
After many experiments, I observed its interaction with various reagents. Under suitable conditions, it can react delicately with specific reagents to generate new products, which paves the way for subsequent research and development.
The road to research and development is difficult and long. However, I uphold perseverance and hope to fully exert the characteristics of this compound. Or it can be used to create new drugs, heal diseases; or in the field of materials, open up new territory. Although the road ahead is long, I am still willing to explore unremitting, hoping to make great achievements and contribute to the development of chemistry.

Toxicity Research

To taste the nature of things, it is important to people. Today there is a thing called 5-Chloro-7-Iodoquinolin-8-Ol, and we should be careful when investigating its toxicity.
If you study its toxicity, you need to observe its response to various things. Observe its harmony with other medicines, or the way it travels in the body, and see if there is any abnormality. If it is applied to plants and trees, it depends on the change of its life and breath; when it is used for insects, observe the change of its behavior.
And the appearance of toxicity does not occur overnight. It may accumulate for a long time, or it will respond when touched. We must record it in detail, from the beginning to the extreme. In this way, Fang Deming 5 - Chloro - 7 - Iodoquinolin - 8 - Ol is the truth of toxicity, for the world to use, to avoid its harm and pursue its benefits.

Future Prospects

Wuguan 5 - Chloro - 7 - Iodoquinolin - 8 - Ol This thing is unique in nature and has considerable development in the future. Although it is currently in the research period, the future seems to be bright. It can be used in the way of medicine, or it can find a way to cure diseases and save people, so as to solve the diseases of everyone. The field of chemical industry may be the foundation for the creation of new things and open the way to innovation.
With time, if the research is advanced and the technology is complete, it will surely shine. It can be used for the development of new drugs and add new branches to the apricot forest; it can also be used for material innovation to add power to the industry. I am convinced that the future of this material will be able to break through the limitations of the present, reach a distant realm, be used by the world, and benefit the common people.

Where to Buy 5-Chloro-7-Iodoquinolin-8-Ol in China?

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Frequently Asked Questions

As a leading 5-Chloro-7-Iodoquinolin-8-Ol 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 5-chloro-7-iodoquinolin-8-ol?

5-Chloro-7-iodoquinoline-8-ol is an organic compound. Its chemical properties are unique and have a variety of interesting characteristics.
First of all, its physical rationality, at room temperature, often solid, mostly crystalline, the appearance of crystal clear, the quality is relatively stable. In solubility, in organic solvents, such as ethanol, ether, etc., there is a certain solubility, but it dissolves slightly in water. Due to the molecular structure, it contains hydrophobic groups such as aromatic rings and halogen atoms, resulting in poor hydrophilicity.
When it comes to chemical activity, its hydroxyl (-OH) is active. It can be esterified with acids. In the case of acetic anhydride, under appropriate conditions, corresponding esters can be formed. In this reaction, the hydrogen atom of the hydroxyl group is replaced by the acetyl group to form a new compound. The process requires the assistance of catalysts, such as sulfuric acid, etc., to promote the smooth progress of the reaction.
In addition, the halogen atom also increases its activity. Chlorine atoms and iodine atoms can participate in nucleophilic substitution reactions. In the case of nucleophilic reagents, such as sodium alcohol, the halogen atom can be replaced by an alkoxy group to form a new carbon-oxygen bond, and novel structures can be derived. In this reaction, due to the difference in electronegativity of the halogen atom, the iodine atom is easier to leave than the chlorine atom. Due to the large atomic radius of iodine and the relatively small C-I bond energy, the reaction is easier to move in the direction of generating substituted products.
In addition, the aromatic ring structure of this compound can undergo electrophilic substitution due to its conjugate system. In case of nitrifying reagents, such as the mixed acid of concentrated nitric acid and concentrated sulfuric acid, nitro groups can be introduced into the aromatic ring to form nitro-substituted derivatives. The density distribution of the electron cloud of the aromatic ring determines the selectivity of the substitution position. In this compound, due to the localization effect of hydroxyl groups and halogen atoms, nitro groups are mostly introduced into specific positions, following the localization rule
Because of its nitrogen-containing atoms in the quinoline ring, it has a certain alkalinity and can interact with strong acids to form salts. This property is also one of its chemical properties. 5-chloro-7-iodoquinoline-8-ol has rich chemical properties, providing many possibilities for research and application in organic synthesis and related fields.

What are the main uses of 5-chloro-7-iodoquinolin-8-ol?

5-Chloro-7-iodoquinoline-8-ol is one of the organic compounds. This substance is useful in many fields.
In the field of pharmaceutical research and development, it may have potential medicinal value. Because quinoline compounds are often biologically active, they can be used as lead compounds for researchers to further explore their efficacy on specific diseases, such as antibacterial, anti-inflammatory, etc. After research and modification, new drugs may be created for human health and well-being.
In materials science, 5-chloro-7-iodoquinoline-8-ol is also useful. Due to its unique structure, it can be used to synthesize materials with special properties, such as optical materials, electrical materials, etc. By using its chemical properties, the properties of the material can be adjusted to meet the special needs of different fields.
Furthermore, in the field of organic synthetic chemistry, this compound is often used as a key intermediate. Scientists can use various chemical reactions to build more complex organic molecular structures based on 5-chloro-7-iodoquinoline-8-ol, expand the variety of organic compounds, promote the development of organic synthetic chemistry, and provide more new compound options for many fields.

What are 5-chloro-7-iodoquinolin-8-ol synthesis methods?

To prepare 5-chloro-7-iodoquinoline-8-ol, there are many methods, and each has its own advantages and disadvantages. The following are common synthesis paths.
First, 8-hydroxyquinoline is used as the starting material. The reaction of shilling 8-hydroxyquinoline with chlorinated reagents such as sulfoxide chloride or phosphorus oxychloride under suitable conditions can cause chlorination at specific positions on the quinoline ring, introduce chlorine atoms, and generate 5-chloro-8-hydroxyquinoline. Then, 5-chloro-8-hydroxyquinoline is combined with an iodine substitution reagent, such as iodine elemental substance, and an appropriate oxidant (such as hydrogen peroxide or periodate, etc.). Through the oxidation iodine substitution reaction, the iodine atom is introduced at the 7th position, and the final result is 5-chloro-7-ioquinoline-8-ol. This pathway step is relatively clear, but the reaction conditions need to be carefully regulated, otherwise it is prone to side reactions and affects the purity and yield of the product.
Second, suitable aniline derivatives can be started from. The quinoline ring structure is first constructed by a series of reactions, such as the condensation of aniline and β-dicarbonyl compounds under acid catalysis to form quinoline derivatives. Then, the obtained quinoline derivatives are chlorinated and iodinated in sequence. The advantage of this strategy is that the construction process of quinoline ring can be regulated to optimize the product structure, but the reaction route is relatively long and complicated, requiring multiple steps of reaction and separation and purification operations, which is easy to reduce the overall yield.
Third, the coupling reaction catalyzed by transition metals. Quinoline derivatives containing chlorine atoms with suitable activity check points can be prepared first, and then catalyzed by transition metal catalysts (such as palladium, copper and other catalysts), which are coupled with iodine substitutes to introduce iodine atoms at the 7th position. This method has the advantages of mild reaction conditions and high selectivity, but transition metal catalysts are expensive, and factors such as catalyst loading and ligand selection in the reaction have a great influence on the reaction and need to be carefully optimized.

What is the market outlook for 5-chloro-7-iodoquinolin-8-ol?

5-Chloro-7-iodoquinoline-8-ol is one of the organic compounds. Looking at its market prospects, it can be seen in many fields.
In the field of medicinal chemistry, such compounds may have unique biological activities. Today, in the process of new drug development, there is a great demand for small molecule compounds with specific structures and activities. The structural characteristics of 5-chloro-7-iodoquinoline-8-ol may make it stand out in pharmacological studies such as antibacterial, anti-inflammatory and anti-tumor. Many studies are exploring novel bioactive molecules as the cornerstone for the creation of new drugs. This compound has a unique structure and may find a place for use in it, so it has potential demand in the pharmaceutical research and development market.
In the field of materials science, with the advance of science and technology, the demand for special functional materials is increasing. 5-chloro-7-iodoquinoline-8-ol can be used to prepare photoactive and electroactive materials due to its specific chemical structure. For example, in the field of organic optoelectronics, it is necessary to develop materials with unique optical and electrical properties, whose structure may endow the material with specific light absorption and emission characteristics, or can participate in the construction of new organic semiconductor materials. Therefore, in the frontier research of materials science and industrial applications, there are also addressable market opportunities.
Furthermore, in the field of chemical synthesis, it can be used as a key intermediate. Organic synthesis techniques often rely on various intermediates to build complex molecular structures. The structure of 5-chloro-7-iodoquinoline-8-ol can be chemically converted to give rise to many compounds with diverse structures. The chemical synthesis industry is constantly pursuing efficient and novel synthesis paths and intermediates. This compound may be favored by synthetic chemists and also has a certain position in the organic synthesis reagent market.
However, its market prospects are also facing challenges. The process of synthesizing this compound may be complicated and costly. If it is to achieve large-scale production and wide application, it is necessary to optimize the synthesis method, reduce costs and increase efficiency. And in biological activity research and material application development, further exploration is needed to clarify its exact properties and application scope. But in general, 5-chloro-7-iodoquinoline-8-ol has considerable market prospects in many fields such as medicine, materials and chemical synthesis, which need to be explored and expanded by scientific research and industry.

How safe is 5-chloro-7-iodoquinolin-8-ol?

5-Chloro-7-iodoquinoline-8-ol, this is an organic compound. When discussing its safety, it should be considered from various aspects such as toxicity, stability, and environmental impact.
The toxicity of this compound needs to be investigated in detail through experiments to see what effect it has on the organism. Or it enters the organism through oral administration, inhalation, skin contact, etc., and then affects its physiological function. For example, in animal experiments, if administered in large doses, it may cause organ damage, abnormal behavior, etc. For the human body, it may irritate the skin and eyes. If inhaled or ingested, it may also damage the respiratory system, digestive system, etc.
Stability again. Its chemical structure may determine its stability under specific conditions. In different temperatures, humidity, and light environments, it may undergo reactions such as decomposition and deterioration. Under high temperatures, or accelerate its decomposition process, generating other unknown products. These products may be more toxic or more unstable. And light may also cause luminescent chemical reactions, resulting in structural changes.
Environmental impact cannot be ignored. If this compound enters the environment, it may affect the survival and reproduction of aquatic organisms and disrupt the ecological balance of water. In soil, or change soil properties and affect plant growth. In the atmosphere, if it volatilizes to form gaseous substances, or participates in atmospheric chemical reactions, it will affect air quality.
In summary, the safety of 5-chloro-7-iodoquinoline-8-ol is complex, and it needs many experiments and studies to carefully investigate its effects on organisms and the environment under different conditions in order to clarify its overall safety.